Drug Search

Passiflora Dose

2011-10-01T06:38:00.003-07:00

Passiflora Dose

Büyüklerde im Laufe des Tages eine beruhigende Wirkung auf 1-2 Maßstab bieten vor den Mahlzeiten eine Stunde vor dem Schlafengehen alınır.Uyku 2 Umfang Störungen in der Getränkeindustrie. Kinder (3 Jahre und älter), wird in kleinen Dosen als von Ihrem Arzt eingesetzt. Einer nach dem 1 / 2 Maßstab sollte nicht mehr gegeben werden.

Nebenwirkungen von Passiflora

2011-10-01T06:38:00.001-07:00

Nebenwirkungen von Passiflora

Passiflora'nın keine bekannten schädlichen Nebenwirkungen.

Passiflora Warnhinweise und Vorsichtsmaßnahmen

2011-10-01T06:37:00.002-07:00

Passiflora Warnhinweise und Vorsichtsmaßnahmen

Bedeutet, dass Benutzer müssen Maschinen, die Aufmerksamkeit erfordern, um die Menschen und stellen die zentrale depressive Wirkung des Medikaments sollte im Auge behalten werden verwenden. Schwangere, kann aber mit einer Empfehlung des Arztes verwendet werden.

Indikationen Passiflora

2011-10-01T06:37:00.001-07:00

Indikationen Passiflora

Unruhe, Angst, Menstruation und Menopause Zeiten seelischer Not und Spannung ist in der Behandlung von symptomatischer Beschwerden wie Schlaflosigkeit eingesetzt.

Passiflora Drug Formula

2011-10-01T06:36:00.000-07:00

Passiflora Drug Formula

Jede 5 ml (1 Teil); Passiflora flüssigen Extrakt 700mg Alkohol, Süßstoff, Saccharose, Protective, Methylparaben, Propylparaben

Epidosin Comp. 10mg 20 dragees

2009-11-04T23:12:00.001-08:00

Drug formula:
1 coated tablet, Active substance: 10 mg Valethamate Bromide. Auxiliary substance: titanium dioxide, castor.

Indications:
Gastro-intestinal cramps, spastic constipation, kardiospazm, stomach and intestinal ulcers finger 12 complaints, mild and moderate in bile and urinary tract cramps, dysmenorrhea, born late in my arm make it easier to open cases, such as.

Warnings and precautions:
Hipertrofilerinde Epidosin prostate, urinary botalmasında can be disruptive. Output of the stomach to empty the stomach more narrow ones may be delayed. This should not be used outside Epidosin megacolon and taşiaritmide.

Side effects:
In rare cases the following side effects may occur. Decreased sweating, skin reddening, heart rhythm changes and challenges are seen in the urine. May exacerbate glaucoma. Higher doses, use machines, or may affect the ability to see traffic.

Interactions:
Amantadine, Quinidine, Tricyclic Antidepressants be desired degree of influence with Epidosin'in rises.

Dose of use:
Dragees are swallowed without chewing Günde3 times 1, is best taken after meals. Measures to be taken in case of overdose: Epidosin cramps antioxidant is a substance. Overdose due to vomiting, nausea and stomach should be washed from time.

Dank 340mg 30 lozenges

2009-11-03T05:32:00.000-08:00

Drug formula:
Dihydroxy aluminum sodium carbonate 340 mg sweetening and Odor transmitter: Saccharose, mint essence

Indications:
With stomach disorders manifested Hiperasidite (heartburn, acid indigestion due, heartburn) in eliminating symptomatic as indicated. In addition, with stomach and duodenal ulcers that can be used in the treatment hiperasiditenin and reflux esophagitis.

Warnings and Precautions:
During the long time use can cause hipofosfatemiye. Hypophosphatemia in more severe form, anorexia, malesiya, muscle weakness and may cause osteomalesi'ye. Pregnant and breastfeeding mothers are actually used in the absolute consideration in consultation with the doctor is available. Use in children under 12 years is not recommended. In patients with chronic renal failure may occur hiperaluminemi. Therapeutic effect is sufficient for 8 tablets per day. Need to be taken more time during operation of hipofosfatemiye may yoktur.Uzun. Hypophosphatemia in more severe form, anorexia, malesiya, muscle weakness and may cause osteomalesi'ye. Pregnant and breastfeeding mothers are actually used in the absolute consideration in consultation with the doctor is available. Use in children under 12 years is not recommended. In patients with chronic renal failure may occur hiperaluminemi. Therapeutic effect is sufficient for 8 tablets per day. There is no more need to be taken.

Side Effects:
When used in high doses can cause intestinal motility by reducing konstipasyona.

Interactions:
As with other antacids containing tetracycline to reduce absorption should not be given drugs. For the same reason a lot of absorption of the drug not be taken together within 1 hour is recommended reduced.

Dosage adjustment:
Dank as chewing tablets have been made. Swallowing tablets be chewed to start immediately gives effect. Cases between the two dishes that require constant treatment and night lying be chewing 1-2 tablets are swallowed.

Diafuryl 200mg 24 capsules

2009-11-02T04:27:00.000-08:00

Drug formula:

Suspension 200mg/5ml Nifuroksazid
100mg Capsules Nifuroksazid

Indications:
Invasive non-bacterial origin (especially E. coli) is indicated for the treatment of acute diarrhea. Diafuryl therapy, rehydration does not make unnecessary treatment (see Warnings and Precautions).

Warnings and Precautions:

- Doctors should not exceed the recommended dose and should not be used more than 7 days. - Diafuryl therapy, rehydration therapy does not make unnecessary. Compensate for losses due to diarrhea plenty of salty and sugary fluids (rehydration fluid) is recommended to be taken. - Systemic effects of hemorrhagic and purulent invasive infective diarrhea powerful antibacterial substances should be used. - Contain Tartrazine sensitivity is due to be used with caution in people. Use in Pregnancy and Lactation Pregnancy Category C. Period. Nifuroksazid 'can be used safely in pregnancy is limited clinical experience shows are not recommended for use in pregnant women. Likewise Nifuroksazid 'pass into breast milk in nursing mothers is unknown and does not exceed the absolute usage is not recommended unless necessary.

Side Effects:
Allergic reactions (such as ekzantemik pustulosis) can be seen. In young children, or, rarely, nausea and vomiting can make.

Interactions:
Interactions with other drugs did not undergo systemic systemic absorbsiyona is expected.

Dose adjustment:

Fort Capsules: 6 years and older children and adults per day in 3 to 4 capsules (600 to 800 mg) in divided doses 2 to 4 times is given. Children under 6 years is recommended to use Diafuryl Suspension (see Contraindications). Overdosage because of systemic absorption is extremely low due to systemic overdose - a toxic effect is expected. However, in such a case is tried to be away from the channel of the drug and symptomatic GI / supportive treatment should be applied. Capsules: 10 years old and older children and adults, a total of 3 times per day 4-8 capsules (400-800 mg) in children between the ages of 1-10, a total of 3 times per day 4-6 capsules (400-600 mg) in children diafuryl suspension is recommended.

Omeprol 20mg 14 capsules

2009-11-01T02:08:00.001-08:00

Omeprol 20mg 14 capsules

Drug formula:
Omeprol in each capsule,
Omeprazole 20 mg Capsules Composition; Dye red iron oxide, titanium dioxide

Indications:
Gastric ulcer, duodenal ulcer, reflux esophagitis, Zollinger-Ellison syndrome and do not respond to treatment with H2 antagonists used to treat stubborn cases of ulcer.

Warnings and Precautions:
Omeprol capsule, the probability of malignant gastric tumors in patients with gastric ulcer and masking symptoms, delayed diagnosis of the disease should not be used. Liver enzymes should be measured during treatment Omeprazolle.

Long period of maintenance therapy in patients with liver failure required dose reduction is recommended. Long-term omeprazole treatment of atrophic gastritis during gastric biopsy rarely been observed in patients. Should not be used in children.

Side Effects:
Abdominal colic, dizziness, paresthesia, fatigue, dry mouth, nausea, headache, diarrhea can result. Very rarely, skin rash may occur. These side effects are usually mild and temporary.

Flatulence, somnolence, arthralgia, muscle weakness, myalgia, blurred vision, peripheral edema, gynecomastia, decreased sense of taste, leukopenia, thrombocytopenia, agitation and depression have been reported.

Interactions:
If used with phenytoin or diazepam capsules Omeprol these drugs will decrease the dose excreted in their re-adjustment gerekebilir.Warfarin can interact with.

Omeprol Dose adjustment

2009-11-01T02:08:00.000-08:00

Unless otherwise recommended by a doctor; Omeprol Capsules should be taken before meals, preferably morning. Gastric ulcer and reflux esophagitis: 1 time Omeprol capsule 20mg per day (1 capsule) dose alınır.Tedavi time is 4 weeks. In the treatment of peptic ulcer recurrence in order to prevent long-term use is objectionable.

Patients who do not respond to treatment with 20 mg per day and do not respond to treatment with H2 receptor antagonists in patients as a single daily dose of 40 mg (2 capsules) as a higher dose can be given. Duodenal ulcers: 1 time per day 20 mg (1 capsule) dose is taken. Ulcer in most patients within 2 weeks to apply iyileşir.Gerekirse 2-week treatment.

Zollinger-Ellison Syndrome: 1 In the beginning, once a day 60 mg (3 capsules) Omeprol alınır.Doz are set according to the patient's condition. Zollinger-Ellison syndrome, a daily dose of up to 180 mg in divided doses can be given in the form.

HIGH DOSE AND TREATMENT: There is no specific antidote. Very high rate of protein is connected with dialysis can not be removed from the blood. In case of overdose, symptomatic and supportive treatment should be made.

Motilium 30mg Dose Adjustment

2009-10-31T14:43:00.001-07:00

Chronic dyspepsia
Adults: 10 ml (or 1 tablet), 15-30 minutes before meals 3 times a day and evening before going to bed is taken when necessary.
Children: 2.5 ml body weight for each 10kg'ı, before meals, 3 times a day and evening before going to bed will be needed
Acute and subacute cases (mainly nausea and vomiting) Adults: 20 ml (or 2 tablets), 15-30 minutes before meals 3 times a day and evening before going to bed is taken when necessary.
Children: 5 ml of body weight for each 10kg'ı, before meals, 3 times a day and evening before going to bed is taken when necessary.

Use Ait Alerts:
Oral alımalıdır motilium before meals. When taken after meals may delay absorption.
In patients with renal impairment, dosage should be reduced frequency (Precautions section below).

Kg-scale for children Use of the Pipette:
- Plastic lid opens.
- Straws in the white outer sheath, with a transparent sheath are removed.
- Transparent pouch inside pipette, dipped into the bottle.
- Transparent cover can be kept constant ring, ring up the upper pipette to withdraw the desired dosage by (or for the child according to weight) is set.
- Pipette inner sheath is removed from the bottle with.
- Private press down into the drugs should be flushed of any beverage.
- Pipette sheath is placed to be used again.

Measures to be taken in dose-out
Symptoms
In cases of overdose, especially in children, drowsiness, extrapyramidal reactions dezoryantasyon and can be seen.
Treatment
Antikolinerjikler, anti-Parkinson drugs or anticholinergic effect of antihistamines can be effective extrapyramidal reactions. There is no specific antidote, implementation and activated charcoal in cases of overdose the patient kept under close supervision is recommended. Symptoms usually pass spontaneously within 24 hours.

Motilium 30mg 6 Suppozituar

2009-10-31T14:40:00.004-07:00

Drug formula:
10 mg Tablet Domperidon
Suspension 1mg/ml Domperidon

Indications:
Fullness in the epigastric region, abdominal bloating, upper abdominal region pain, belching, gas, bloating, nausea, vomiting, heartburn (stomach contents come out of the mouth with or alone) in gastric emptying, such as delay, gastroözofajeal reflux, and together with özofajitle dyspeptic symptoms complex.

Functional, organic, infectious, or from the diet of radiotherapy and drug treatment of nausea and vomiting leading.

Motilium 30mg Interactions

2009-10-31T14:40:00.003-07:00

Anticholinergic drugs, anti-dyspeptic Motilium'un can eliminate the effect. Antacid and anti-secretory drugs, reduces oral bioavailability, and suspension motilium tablets should not be taken at the same time (Precautions section below). Motilium In theory, due to gastro-kinetic effects, the oral drugs are applied, particularly controlled release or may affect the absorption of enteric-coated formulation.

However, blood levels of digoxin or paracetamol and constant access to has been applied in individuals with domperidon use, these drugs do not affect blood levels. Motilium following drugs may be related:
does not increase the effects of neuroleptics,
dopamine agonists (bromocriptine, L-dopa) from the central effects of inhibiting unwanted digestive problems, nausea, vomiting, peripheral effects such as printing.

Motilium 30mg Interactions

2009-10-31T14:40:00.002-07:00

Motilium 30mg Side Effects

2009-10-31T14:40:00.001-07:00

Rare side effects can be seen as a temporary abdominal cramps have been reported. Extrapyramidal effects in young children, rare, very rare in adults: treatment and completely spontaneously returns to normal after discontinuation.

The pituitary gland is located outside the blood-brain barrier, may cause an increase in motilium prolactin levels. Rarely, this hyperprolactinemia, galactorrhea and gynecomastic cause. Mature blood-brain barrier (in babies) or is damaged, neurological side effects can not be completely ignored. Rarely, rashes, allergic reactions such as hives have also been reported.

Motilium 30mg Warnings and Precautions

2009-10-31T14:40:00.000-07:00

Used in conjunction with antacid and antisekretuvarlar motilium, these drugs must be taken after meals not before, simultaneously with motilium tablets or suspension alnmamalıdır.
Use in children: the first months of life in the body's metabolic and blood-brain barrier function is not fully developed, infants in the control of any drug should be administered with caution and physicians. Motilium, it does not pass the blood-brain barrier, does not cause neurological side effects, one is given to children under the age of such side effects should be careful in case.

Liver Patients Use: Large percentage is metabolized in the liver, in patients with liver failure, should be careful when using motilium.
Kidney Patients use: serious renal failure that (serum creatinine value of> 6 mg / 100 ml,> 0.6 m mol / l) in patients domperidonun elimination half-life of 7.4 hours to 20.8 hours longer, but plasma levels in healthy individuals is low. A very small fraction of the drug is excreted in urine unchanged in patients with severe renal failure dose modification of a single application is required.

However, applications that can be repeated, depending on the severity of renal failure, one or two times a day by applying the drug, the dose can be reduced. Overall, patients in long-term treatment on a regular basis will be evaluated.

Use in Pregnancy and Lactation Period: The observations in experimental animals 160 mg / kg / day as high doses, teratogenic effects of medication has been found. However, like many drugs Motilium'da pregnancy trimestrinde the first, is more than likely be given the benefit of risk. So far not been shown in humans with increased risk of malformation. Passes into breast milk of nursing rats (mostly in the form of metabolite: 2.5 mg / kg oral and intravenous obtained the highest concentrations applied, respectively, 40 ng / ml and 800 ng / ml). In women, breast milk concentrations of plasma concentrations of domperidon is 4 times.

Whether this concentration is harmful to the newborn is unknown. Therefore, the risk of motilium use of mothers, but more than likely when the benefits of breastfeeding is recommended. Tools and Machinery to Use Effect: motilium, when used in recommended doses does not affect psychomotor activity.

ide-intestinal bleeding, perforation of the digestive system, gastro-intestinal mechanical occlusion and after surgery is not used. Pregnancy and lactation is not used unless necessary in certain. Anticholinergic drugs are used together.

Duspaverin 100mg 50 dragee

2009-10-30T01:22:00.001-07:00

Pharmaceutical Formulation:

Each contains the active ingredients coated tablet 100 mg Mebeverin HCl. Supporting materials: titanium dioxide and sugar.

Indications:

Columns of functional disorders;
- Primary irritable bowel syndrome, the following secondary causes of irritable bowel syndrome:
- Regional enteritis (Crohn's Disease)
- Abdominal pain
- Divertiküloz and diverticulitis
- Gallbladder disease (bile diskinezisi)
- Stomach and duodenal ulcers
- Specific or non-specific inflammation of the digestive tract, enteritis, such as dysentery.

Warnings and Precautions:
Teratogenic effects of the results of the experiments has not been found. Alone, as other drugs during pregnancy should be cautious when using the Duspaverin.

Using dose:
In the elderly, adults and children over the age of 10; 1 coated tablet 3-4 times per day (100 mg) 20 minutes before meals should be taken. On the desired effect within a few weeks when the dose of the drug should be reduced gradually.

Overdosage: In case of overdose in experiments on animals the central nervous system eksitasyonu can be expected. There is no known antidote. Of the stomach is recommended to be washed and symptomatic treatment is recommended.

Duspaverin side effects

2009-10-30T01:22:00.000-07:00

No side effects when used within the specified doses is not.

Famodin 40mg 30 tablets

2009-10-28T01:13:00.006-07:00

Drug formula:
Each tablet; Famotidine
Article 20.40 mg Coating Ingredients: titanium dioxide, iron oxides

Interactions:
Required in humans, as well as animal models and in vitro studies with liver enzymes mikrozomal (eg cytochrome P450 system), which metabolize drugs among Famotidine did not reveal a significant interaction.
Among the tested drugs warfarin, theophylline, phenytoin, diazepam, antipyrine aminopirin and can be considered. Is no carcinogenic or mutagenic effects, does not affect fertility adversely.

Famodin 40mg Dose Adjustment

2009-10-28T01:13:00.005-07:00

Unless otherwise recommended by a doctor;
-Acute treatment of duodenal ulcer: The recommended oral dose of 40 mg of active ulcer duedenal (2 tablets) and at a time before going to bed most alınır.Hastaların longer than 4 weeks iyileşir.Nadiren 6-8 weeks should be continued. Uncomplicated active duodenal ulcer at 8 weeks Famodin'in long-term use has not been determined yet reliability. 20 mg in the morning and evening is equally effective.

Maintenance therapy; recommended oral dose of 20 mg (1 tablet) and at a time before going to bed alınır.Aktif ulcer healing after low doses of patients with duodenal ulcer treatment, but controlled studies are limited to 1 year. Short-term treatment of active benign gastric ulcer-doses, acute treatment, the recommended dose for adults 1 a day is 40 mg before bed time. Longer than 8 weeks of use Famotidinin reliability and safety has not been established.

Be used in the treatment of short-term dose-Gastroösofageal reflux; gastroösofageal reflux symptoms in people who show 2 times a day 20 mg (1 tablet) at a dose of 6 weeks duration to apply. These symptoms are also accompanied by erosion and ülserasyonda the recommended doses, twice a day for 12 weeks and 20 (1 tablet) or 40 mg (2 tablets) capability. Pathological case of hipersekresyon (Zollinger-Ellison syndrome and multiple endocrine adenomalar): Recommended starting dose of 6 hours 20 mg (1 tablet) capability.

Some patients may need a higher dose to start with. Dose is adjusted to the needs of the patient and clinical treatment as long as is necessary in some patients with more edilir.Ağır Zollinger-Ellison Syndrome with a 160 mg dose of 6 hours were used. Renal failure dose adjustment: severe renal failure (creatinine clearance 10 ml / min) Famodin'in elimination half-life may exceed 20 hours and could take up to approximately 24 hours in patients anürik. Although Famodin'in side effects and plasma concentration or the relationship between certain drug to prevent the accumulation of, Famodin'in dose should be reduced (20 mg before bedtime), or time between doses, the patient's clinical response compared to 36 to 48 hours should be removed.

And TREATMENT OF EXCESSIVE DOSE: 640 mg per day for patients in pathological cases hipersekresyon doses given up to serious side effects and accidental overdoses of çıkmamıştır.İstemli purchases symptomatic and supportive treatment should be applied. Yet non-absorbent material must be removed from the digestive system (to induce vomiting, lavage) by monitoring the patient's vital functions, supportive treatment should be continued. Hemodialysis can not be removed from the body.

Famodin 40mg Side Effects

2009-10-28T01:13:00.004-07:00

The following side effects of patients treated with Famotidine in more than 1% and the drug may have emerged.
Headache (4.7%), dizziness (1.3%), constipation (1.2%) and diarrhea (1.7%). Famotidine depending In clinical trials they found exactly the rarely in the following side effects have been reported.
Systemic fever, asthenia, fatigue
Cardiovascular; palpitations
Gastrointestinal nausea, vomiting, abdominal pain, loss of appetite, dry mouth, pathological changes in liver enzymes
Hematological; thrombocytopenia Hypersensitivity; orbital edema, redness konjuktivada musculoskeletal system, muscle-skeletal pain, joint pain
Nervous system / psychiatric, paresthesia, depression, anxiety, libido decreased, sleep disorder
Respiratory system; bronchospasm
Skin; alopecia, acne, itching, skin dryness, redness
Sense organs; tinnitus, taste disorder
CONSULT YOUR DOCTOR IF AN UNEXPECTED EFFECT ENSUES.

Famodin 40mg Warnings and Precautions

2009-10-28T01:13:00.003-07:00

Famotidine treatment will be provided with the possibility of symptomatic improvement of gastric malignancy in the middle kaldırmaz.Ağır renal failure (creatinine clearance 10 ml / min) 2 extend the time interval between doses or low doses should be used.

However, due to toxicity in the plasma concentrations of high-Famotidine event so far has been found. Use during pregnancy and breastfeeding: But there are absolute indications should be used under close medical supervision. Used by children; Famotidin'in use efficiency and reliability in children has not been determined yet. Does not require dosage adjustment in elderly patients.

Famodin 40mg Indications

2009-10-28T01:13:00.001-07:00

Short-term treatment of duodenal ulcer 1.Aktif.
2.Aktif ulcer healing after low doses in the treatment of patients with duodenal ulcer.
Short-term treatment of benign gastric ulcer 3.Aktif.
4.Gastroösofageal reflü'nün short-term treatment.
Case in the treatment of 5.Patolojik hipersekresyon (Zollinger-Ellison syndrome, multiple endocrine adenomalar).

Gastrofam 40mg 30 tablets

2009-10-18T15:44:00.003-07:00

Drug formula:
Each film-coated tablet, 40 mg Famotidine, dyestuffs as titanium dioxide, iron oxide and yellow iron oxide contains.

Indications:

Gastroduodenal ulcer -
-Gastric ulcer since
-Zollinger
-Ellison Syndrome
-In protection of duodenal ulcer recurrence

Interactions:

Any interaction with other drugs among Famotidine has not been determined. Be supplied with antacids if necessary. Famotidine 'alınımından then applied at a dose of 20 mg Procainamid' in and has not been any changes in major metabolitilnin tubular excretion. Famotidine during the uygulanımı warfarin, theophylline, nifepidin, metaprolol, antipyrine, biological degradation processes in the body of drugs such as aminopirin any differences arise not.

Gastrofam 40mg Dose Adjustment

2009-10-18T15:44:00.002-07:00

Gastroduodenal ulcer: Start therapy: The recommended dose is 40 mg at night before going to bed 'lık Gastrofam a tablet obtusa. Duration of treatment is 4-8 weeks. Required duration of treatment may be shortened compared to controls. In many applications, at the end of a 4-week treatment of duodenal ulcer is seen improves. The first 4 weeks after the ulcers in the control good if treatment is continued for 4 weeks.

Maintenance therapy: Duodenal ulcer 20 mg before bedtime to prevent recurrence 'lık maintenance therapy with Famotidine is performed. This treatment is continued over 6 months. Gastric ulcer start: The recommended dose of 40 mg the evening before going to bed 'lık Famotidine a tablet is. Shorten the duration of treatment compared to controls with is 4-6 or 8 weeks. Zollinger-Ellison syndrome: Previously untreated acid secretion in patients with no preventive treatment given 6 hours or 1 ½ tablet 40 mg to 20 mg per tablet is.

Dose according to patient's condition and treatment time is increased according to clinical indication is extended. AND TREATMENT Overdosage: applications in experimental animals Famotidine in selective and non-relative as a drug that has proven to be toxic. As a result of accidents in people who received severe doses to patients tüksek general symptomatic and supportive treatment should be applied, if necessary Famotidine in plasma by hemodialysis in clearing should be provided

Gastrofam 40mg Side effects

2009-10-18T15:44:00.001-07:00

Was well tolerated in large-scale clinical trials were found. Headache, dizziness, constipation, diarrhea, flatulence, nausea, anorexia seen in side effects such as rate of 1% is below.

Mouth, skin rash, abdominal discomfort may be present. Be seen as a very rare side between ethical mild elevation of transaminase levels, side effects such as hallucinations oryontasyon disorder and can be counted.

Gastrofam 40mg Warnings and Precautions

2009-10-18T15:44:00.000-07:00

Famotidine in the treatment of gastric ulcer before starting the malignant ulcer must be tempered not definitely proven. Otherwise, the stomach cancer symptoms and thus diagnosis to be masked may result in the delay. Especially in long-term treatment, in terms of impact and possible side effects patients should be monitored periodically by the physician.

Dose adjustment should be performed in the elderly. Safety and efficacy in children has not been determined yet. Use in pregnancy: Gastrofam, as well as all other drugs, during pregnancy and lactation, but it was really necessary in cases under doctor's orders and control should be used.

Nevofam 20mg 60 tablets

2009-10-17T11:39:00.001-07:00

Drug formula:
Each tablet contains 20-40 mg Famotidine.

Indications:
Duodenal ulcer, gastric ulcer Selim, Repeater ulceration, gastritis, reflux esophagitis, Zollinger-Ellison syndrome, multiple endocrine adenoma hipersekresyon pathological conditions such as

Warnings and Precautions:
Severe renal insufficiency (creatinine clearance <10 ml / min) in subjects with a lower dose or dose range extension of the application may be required. Pregnancy and breast-feeding duration and usage safety in children has not been established.

Side Effects:
Rarely headache, dizziness, skin rashes, dry mouth, nausea, vomiting, flatulence, loss of appetite, diarrhea and constipation may occur.

Interactions
P-450 enzyme system and metabolized NEVOFAM tablet that does not interact significantly with medication.

Dose adjustment:
Duodenal ulcer 1x40 mg per day (at night before bedtime), for a period of 4-8 weeks; Selim 1x40 mg a day in gastric ulcer (night before bedtime), for a period of 6-8 weeks; Repeater in duodenal ulcer prophylactic 1x20 mg a day (at night before bed) ; Zollinger-Ellison syndrome 4x20 mg per day is recommended, including pathological hipersekresyonlarda. Overdosage Measures to be taken in the drug treatment and support will be removed from the stomach.

2009-10-16T04:33:00.003-07:00

------------------------------------------------
Side Effects 1mg 10 film tablet Setron
40 mcg / kg dose granisetron uygulamasınan after 7-day period of side effects observed in 1268 patients have been examined in a study covering 14% headache, asthenia 5%, dizziness 4%, diarrhea 4%, and constipation was found in 3%.

2-160 mcg / kg dose of granisetron is applied in more than 3000 patients evaluated the results of the study as the various organ systems according to the following side effects were observed: liver: Comparative studies of patients with 2.8% in the AST and 3.3% at the rate of normal ALT levels 2 times the values that go above been reported cardiovascular system: hypertension was found in 2%.

Hypotension, arrhythmias such as sinus bradycardia, atrial fibrillation, AV block in varying degrees, including uncontrolled tachycardia and ECG ectopia was seen as rare disorders. Central nervous system: Agitation, anxiety, CNS stimulation and insomnia were seen in less than 2% of patients. Other side effects: Fever 3%, taste disorders, 2%, skin rashes were seen in 1%.

Interactions 1mg 10 film tablet Setron

2009-10-16T04:33:00.002-07:00

Does not induce cytochrome P 450 enzyme system, Granisetron, or does not inhibit. Pharmacokinetic and pharmacodynamic interactions with other drugs Granisetronun for review does not have any specific studies.

However, the antiemetic granisetron in the treatment frequently used benzodiazepines, neuroleptics and has been used safely in conjunction with antiülser preparations. Liver cytochrome P 450 system Granisetron is metabolized by this system are made on the inhibition or induction, and therefore half-time clearance of drugs granisetronun change.

Setron 1mg 10 film-coated tablets

2009-10-16T04:33:00.001-07:00

Drug formula:
In each bulb (3 ml), Granisetron (as granisetron hydrochloride) 3 mg Sodium chloride 27 mg, water for injection qs

Indications:
Cancer therapy and cytostatic treatment Emetojen caused nausea and vomiting is indicated for the prevention and treatment.

Warnings and Precautions:

Granisetron reduced bowel movements, Setron after application of the common symptoms of subacute intestinal obstruction patients should be monitored. Use in Pregnancy and Lactation period category B in pregnancy is classified as Granisetron. Teratogenic effects in studies on animals or no negative impact on fertility has not been found. However, for the use of granisetronun in humans during pregnancy there are no adequate well-controlled studies in pregnant women absolutely Setron should not be used if not required.

Pass into breast milk is not known whether Granisetronun. Many drugs pass into breast milk because breast-feeding should be careful in those cases the use of granisetron. Intravenous use in children under 2 years in pediatric patients granisetronun use efficiency and reliability are not shown. Efficiency and reliability in elderly Granisetronun use in elderly patients is similar to adults.
Dosage adjustment:
Adults Setron of ampoule 10 mcg / kg dose chemotherapy in the previous 30-minute time period before the implementation is recommended. IV bolus in 30 seconds, the bulb Setron diluted or 0.9% sodium chloride or 5% dextrose with 20-50 ml total volume to be diluted in 5 minutes infusion may apply. Created immediately before the application of diluted solution preparation is recommended.

However, 0.9% sodium chloride or 5% dextrose solution was prepared at room temperature, diluted with normal lighting conditions are stable for a period of 24 hours. Children between the ages of 2-16 in children with 10 mcg / kg dose is recommended. Children under 2 years of use Granisetron has not been investigated. Senior citizens are not required for senior special pozoloji.

Used as specified in adults. Patients with kidney or liver failure in patients with kidney or liver failure do not need a special pozolojiye. Overdosage In case of overdose Granisetronun There is no specific treatment. In case of overdose symptomatic treatment should be applied. Up to 38.5 mg no symptoms in the use of granisetron overdose is not seen or been reported mild headache.

Anti-Vomit 200mg 20 film tablet

2009-09-30T03:44:00.001-07:00

Drug formula:
100mg Trimetobenzamid Bulb 1
200mg Coated Trimetobenzamid

Indications:
Keep vehicles, infection, intoxication, vomiting of pregnancy, hepatitis, drugs that cause nausea, cholecystitis, is indicated in migraine.

Warnings and Precautions:
Motor vehicles, etc. that may occur due to sleep. Use those, working in high places patients should be warned. Benzamide is not used in susceptible patients.

Side Effects:
Convulsion, hypersensitivity reactions, parkinsonism symptoms, weakness, inkoordinasyon, headache, blurred vision, irritation and side effects like dry mouth may occur.

Interactions:
Studies in experimental animals has been Antepsin'in (sucralfate) with tetracycline and phenytoin are used to a significant decrease of these drugs showed biyoyararlılığında.

In this respect, may inhibit the absorption of certain medicines in tablet Antep in mind, other drugs taken separately is recommended.

Using dose:
Lamp: In adults, only i.m. day 3-4x1 is applied as a light bulb. Dragee: day 3-4x1 coated tablet in adults is applied. Lying in the night and morning one dragee kalknca pregnancy is used.

Pariet 20mg 28 tablet

2009-09-29T06:11:00.003-07:00

Drug formula:
Rabeprazole sodium, 10-20 mg

Pariet Indications:
Active duodenal ulcer, active benign gastric ulcer or ulcerative erozif symptomatic treatment of reflux gastroözofajal.

Pariet Warnings and Precautions:
And as a whole must not be violated without breaking the tablets should be used. In children is not recommended. Severe liver dysfunction, those should be used with caution.

Pariet Side Effects:
Headache, diarrhea, abdominal pain, asthenia, flatulence, rash and dry mouth

Interactions Pariet:
The compound-dependent absorption in the stomach pH'sına serum etkileşebilir.Ketokonazolün may cause an increase in the level of azaltabilir.Taban digoxin level.

Pariet Dose Adjustment

2009-09-29T06:11:00.001-07:00

In the treatment of active duodenal ulcer and active benign gastric ulcer 1x1 tablet daily dose is to be taken in the morning.

In the treatment of active duodenal ulcer duration of 4 second 4-week treatment period haftadır.Gerektiğinde may apply.

In the treatment of active benign gastric ulcer cure period 6 haftadır.Gerektiğinde is repeated. 4-8 weeks for ulcerative gastroözofajial reflux Erozif or 1x20 mg per day on an empty stomach in the morning kullanılır.Tabletler should be used. Renal and hepatic impairment dose adjustment is required ones.

Intestinol 120 Coated

2009-09-28T03:05:00.001-07:00

Drug formula:
In each enteric coated tablet coated Pancreatin: 59.4 mg ox bile: 21.3 mg Medicinal Carbon: 71.1 mg Assistant Ingredients: titanium dioxide

Indications:
Dyspepsia, gastro-like symptoms, digestive system, gas watch Cardial bile and the enzyme deficiency, common postoperative digestive insufficiencies, kolesistopatiler, pancreas insufficiencies, fatty diarrhea and radiological examinations before the gas is used to resolve.

Warnings and Precautions:
Before using external pancreatic enzymes, the primary cause of indigestion should be investigated. Drug intake should be discontinued when symptoms on sensitivity.

Bicarbonate in patients with pancreatic insufficiency with diarrhea should be given control of a antiasid. Use in pregnancy: This topic is not enough work should be used only if absolutely necessary.

Side Effects:
Nausea and diarrhea in high doses may be tried. Rarely, allergic reactions, and hyperuricemia may cause görülebilir.Çok high doses hiperürükozüri.

Interactions:
Should not be used in patients on oral iron therapy.

Using dose:
Otherwise advised by doctors not to use, 3 times a day, 3-4 coated tablet should be taken with food.

Dragee for, without chewing should be swallowed whole with some water. Preparation of radiological examinations in order to be given to the patient survey should be initiated İntestinol from 1-3 days ago.

HIGH DOSE TREATMENT: High doses may cause diarrhea, nausea and use, it should be measures and gastric lavage should be performed if necessary.

Alin 250mg 20 tablets

2009-09-27T12:50:00.000-07:00

Drug formula:
Phenolphthalein Tablet 0.25g

Indications:
Acute and chronic constipation are used. And x-ray examination before their discharge from bowel surgery indicated.

Warnings and Precautions:
Used during pregnancy and lactation. Rectal bleeding, congestive heart failure, colostomy, ostomi, hypertension and diabetes mellitus'ta used with caution.

Urine color, should be reported to the patient değiştirebilecegi. Diuretics, M suplementleri, spironolactone, and will not be used in conjunction triamterenle.

Side Effects:
Allergic skin rash and especially side effects such as fixed erythema and skin pigmentation can be seen.

Dose adjustment:
In adults, 3x1 tablet / day
In children, 3x1 / 2 tablet / day dose, 2 hours before or after meals is used.

Ranitab 150mg 60 film tablet

2009-09-19T09:07:00.003-07:00

Drug formula:
Bulb 1 ranitidine hcl 50mg
Film-coated tablet 150mg ranitidine hcl 1
Flim ranitidine hcl 300mg tablet

Indications:
In duodenal ulcer, gastric ulcer, the ulcer in Anastamoz, duodoninin rezidiv Ulcus ventriculi and ulcus prophylaxis, reflux ösofajitte Zollinger-Ellison syndrome, with a single dose is indicated for the prevention of birth during the acid aspiration.

Warnings and precautions:
Before starting the treatment of malignant gastric ulcers and should be investigated. Renal and hepatic failure and the dose should be reduced in the elderly.

Ranitab dose adjustment

2009-09-19T09:07:00.001-07:00

Usual dose, morning and evening before going to bed 2x150 mg / day dose is 300 mg or a single dose before bedtime. 150 mg applied again before going to bed at night. Prevention of acid aspiration anesthesia a few hours ago 1 tablet in Zollinger-Ellison syndrome 3x150 mg per day should be used. 600-900 mg / day up to removable. Duration of treatment 4-6 weeks in uncomplicated cases and complicated cases for 8 weeks.

Preparations are used in cases of acute form of the bulb. Duodenal ulcer, gastric ulcer and gastric ulcers occur after surgery in the treatment of acute: 150 mg per day or 1 times 2 times 300 mg. Reflux ösofajitte: 150 mg per day or 1 times 2 times 300 mg. The duodenum and stomach ulcer prophylaxis rezidiv: 150 mg before bedtime. Single dose prevention of acid aspiration: from 2 hours before the start of anesthesia or the birth of 150 mg is given orally, and this dose should be repeated at intervals of 6 hours.

Zollinger-Ellison syndrome, gastric acid secretion, such as very high in cases where: treatment 3 times a day and maintenance dose is 150 mg per RANİTAB given to the patient's status is adjusted. Up to 6 g daily dose requiring upgrade of cases have been reported. Treatment duration: 4 weeks in the stomach and duodenum ulcer, reflux ösofajitte for 8 weeks. Night, lying in the cases of recurrence 1 a day times 150 mg given RANİTAB maintenance therapy can be applied.

Duphalac Solution 670Mg 250ml

2009-09-17T10:17:00.005-07:00

Drug formula:
Lactulose, 670 mg / ml

Indications:
Constipation conditions: normal physiological rhythm Duphalac win column allows.
Portal systemic encephalopathy: treatment and prophylaxis of hepatic protection and prekomanın is used.
Consistency of the stool is soft when medically desirable conditions
(hemorrhoids, cologne, after surgical interventions for in the anus).

Interactions:
Laktülozun column due to lower pH, pH dependent colonic release of drugs (5-ASA preparations containing some) may cause inactivation.

Duphalac side effects

2009-09-17T10:17:00.004-07:00

The first few days the feeling of bloating may occur. These effects usually disappear 1-2 days. Used in higher doses than recommended abdominal pain and diarrhea may occur. In this case the dose should be reduced. Depending on the diarrhea, electrolyte imbalances may be present levels.

Duphalac warnings and precautions

2009-09-17T10:17:00.003-07:00

Constipation status a few days despite treatment does not improve or if any physician should be consulted again.

In patients with lack Lakdoz is used preparations of this enzyme deficiency is associated with the sugar content should be taken into consideration.

The recommended dose for patients with constipation in diabetes does not present a problem. hepatic coma and in such cases usually prekoma much higher doses are used, these doses can be problematic in patients with diabetes. Safely used during pregnancy and lactation.

Duphalac dose adjustment

2009-09-17T10:17:00.001-07:00

Daily dose should be determined individually. Generally, the daily dose in adults since daily maintenance dose of 15-25 ml 15-45 ml
Children (7-14 years) to get started daily doses of 10-15 ml daily maintenance dose of 15 ml
In years 1-6: Start as a daily dose of 5-10 ml, the maintenance daily dose of 5-10 ml, 5 ml per day in infants starting and sustaining 'dir. Patient dose can be reduced by gereksimine.

Hepatic coma and prekomada dose: Starting dose of 30-50 ml 3 times a day, maintenance dose: 2-3 times per day should be set to provide a soft defekasyon. Fecal pH 5.0-5.5 and preferably should be.

Using Pankreon Dose

2009-09-16T17:11:00.002-07:00

Meals unless otherwise advised Pankreon Compositum dragee 1-3 pieces. Should be taken between meals are dragee chewing.
If you need higher doses or even outside the meals can be taken.

Pankreon Comp. 20 Dragees

2009-09-16T17:11:00.001-07:00

Pharmaceutical Formulation:
Coated 1; active ingredients: Pancreatin (8000 Lipase - 6500 Amylase - 450 Protease F.İ.P. Unit)
212.5 mg Dispert Safra
50.0 mg Excipient: Powdered sugar, titanium dioxide

Warnings and Precautions:
Be used in pregnant women and nursing mothers, the relationship between benefits and loss taken into account as should be used.

Side effects:
Içersindeki preparations of substances, especially proteins with known hypersensitivity should be used with caution in people.

Indications Pankreon

2009-09-16T17:11:00.000-07:00

Mild and severe digestive disorders, pancreatic insufficiency, gastric noble (lack of digestive juice), liver and biliary tract diseases due to digestive disorders, stomach and digestive disorders after bowel surgery, mukovisidoz.

Duspatalin Dose Adjustment

2009-09-15T18:59:00.005-07:00

Adults and older children under 10 years:
Meals 3-4 times per day 100 mg mebeverin preferably 20 min. should be taken before.
A few weeks later to obtain the desired effect when the dose should be reduced gradually.
Should not be used in children under the age of 101. Keep out of reach of children here in its packaging.

Duspatalin 100mg 50 dragee

2009-09-15T18:59:00.003-07:00

Drug formula:
Mebeverin HCl, 100 mg

Warnings and Precautions:
The use of any drug during pregnancy ilşkin measures must be supervised.

Side Effects:
Dose used in the treatment of side effects has not been reported for any Duspatalin'e.

Indications Duspatalin

2009-09-15T18:59:00.001-07:00

Spastic colon irritable bowel syndrome primary functional disorders,
Following secondary causes of irritable bowel syndrome,
Divertüküloz and diverticulitis,
Regional enteritis,
Gallbladder disease,
Stomach and duodenum ulcer, digestive specific or nonspecific way iltihablar, enteritis, such as dysentery.

Asacol 800mg 90 tablets

2009-09-14T16:37:00.004-07:00

Drug formula:
Each gastro-resistant tablets; Mesalazin (5-aminosalicylic acid )....... 400 mg contains. Assistant Ingredients: Lactose, Modified starch, Mg. Stearate, Talk, Povidone, Metakrilik acid-Metilmetakrilat copolymer, Trietil citrate, iron oxides and Makrogol 6000

Indications:
Mild and moderate ulcerative colitis, Asacol tablets provide and ulcerative colitis in remission and is used to maintain remission in Crohn's disease.

Using dose:

Ulcerative colitis: remission in adults divided doses per day to provide 2.4 - 4.8 g is used. Day to maintain remission 1.2 - 2.4 g in divided doses is given. Crohn's Disease: The recommended dose for maintaining remission and 2.4 g is divided. For children a special dose recommendation is not available.

Tablets to be taken by mouth and should be swallowed whole without chewing, and without breaking. Ideally, the tablets should be taken before meals with a glass of water. Overdosage AND MEASURES: Signs and symptoms seen in cases of salicylate intoxication are expected to be similar.

Mixture of acidosis-alkalosis: hyperventilation, pulmonary edema, sweating and vomiting, dehydration and hypoglycemia results. Acidosis-alkalosis mixture treatment: According to the special case of acid-base balance and electrolyte losses should be corrected must be met. Sweating and vomiting, dehydration results: liquid should be given. Hypoglycaemia: glucose should be given. Stomach wash is done and also to increase diuresis are given intravenous electrolyte solutions. There is no specific antidote.

Asacol interactions

2009-09-14T16:37:00.003-07:00

Mesalazin reduce digoxin absorption. Effects of azathioprine and 6-merkaptoprinin immunosupressed Mesalazin may increase. At the beginning of such a combination therapy, blood counts should be monitored by repeating particular the number of leukocytes and lymphocytes.

Probenecid and sülfinpirazonun urikozürik effect, diuretic effect of furosemide and spirolakton effect may be reduced. Gastrointestinal side effects of glucocorticoids may increase. May inhibit the effect of warfarin Mesalazin. If you see this combination are indispensable prothrombin time should be monitored closely.

Asacol side effects

2009-09-14T16:37:00.002-07:00

Side effects seen in clinical treatment with ASACOL usually mild and transient. Short-term (6 weeks) placebo-controlled study of patients ASACOL group, 3.2%, while the placebo group, 2.2% had stopped treatment. In this study, 2% on a frequent major side effects: Headache, abdominal pain, belching, pain, nausea, pharyngitis, diarrhea, asthenia, dizziness, back pain, fever, skin rash, dyspepsia, rhinitis, arthralgia, hypertonia , vomiting, constipation, flatulence, dysmenorrhea, chest pain, chills, fever and peripheral edema.

Among these, only "skin rash" has shown a tendency to increase with increasing dose ASACOL. 3342 patients, including uncontrolled clinical study, 5% above the commonly reported and ASACOL dose increased with the increasing incidence of side effects are: Asthenia, fever, flu syndrome, pain, abdominal pain, flatulence, gastrointestinal bleeding, back pain, arthralgia, and rhinitis.

Asacol Warnings and Precautions

2009-09-14T16:37:00.001-07:00

In patients with kidney disease are not recommended for use and production of blood in patients with elevated proteinuria, which should be used with caution. Developed during treatment in patients with kidney dysfunction caused mesalazinin nephrotoxicity should be considered. Before starting treatment Asacol and periodically during treatment with Asacol in patients with renal function examining all recommended.

These tests should be done within 14 days after starting treatment and then 4 weeks should be repeated 2-3 times. If the result is normal tests can be done every 3 months. If new symptoms occur if control tests should be repeated. If the lung function impairment should be monitored especially closely astmada patients. With regard to these preparations have been reported very rarely serious blood diskrazileri.

If you can not be explained in a patient with bleeding, bruising, purpura, anemia or hematological tests should be made if fever developed. If you have signs of blood or suspected diskrazisi treatment should be interrupted immediately and the patient must consult a doctor. Pregnancy and Lactation Usage: pregnancy risk category B.. Teratogenic effects in animal studies or from mesalazinden related toxicity on the fetus showed.

Regarding use in pregnancy limited Mesalazinin clinical research on pregnancy and the fetus showed no harmful effects. Human breast milk at low concentrations and low concentrations mesalazin its N-acetyl metabolite were found. The clinical significance has not been determined, the mesalazin given to nursing mothers should be careful. Use in the elderly: Mesalazin only for patients with normal renal function is recommended and should be used with caution (see warnings).

Polivit 100ml syrup

2009-09-13T00:26:00.001-07:00

Drug formula:
5 Do you (1 part) Polivit Syrup, active ingredients as: Vitamin A 1500 IU Vitamin B1 1 mg Vitamin B2 (Sodium Phosphate) 1.2 mg Vitamin B6 2 mg Nicotinamide (PP) 7 mg D-Panthenol 3 mg Vitamin C 25 mg Vitamin D3 400 IU Vitamin E 5 mg Auxiliary substances: sugar and sodium SACCHARIN, also methyl paraben, propyl paraben and sodium benzoate contains.

Warnings and Precautions:
When taken in high doses and long periods may cause hipervitaminoza should not be forgotten. Because of possible teratogenic effects, high doses of vitamin A intake during pregnancy should be avoided.

Side effects:
In the case of long-term use of excessive doses side effects may occur due hipervitaminoza. Allergic skin rash, mucosal ulcerations and rarely sensation of heat that can be seen, side effects may occur, such as feeling faint.

Interactions:
Vitamin A, you can create side effects increased with Retinoid containing products. Barbiturate and antikonvülsanlar, Vitamin D may reduce the effect of D's. Niacin, ganglionik blockers may increase the hypotensive effects. Vitamin B6, Erlich reagent may give inaccurate results in the determination ürobilinojen.

Using dose:
By the physician unless otherwise recommended: 3 months-1 between the ages of children: day 5 ml (1 part) 1-5 between the ages of children: 7.5 ml per day (1.5 scale), 5 years old and older children and adults: 10 ml per day (2 scale) , pregnant mothers and milk: 10 ml per day (2 scale). Overdosage: accidental or intentional overdose is received, the symptomatic treatment and supportive therapy discontinuation of the drug is applied.

Polivilit indications

2009-09-13T00:26:00.000-07:00

- Nutrition disorders in children observed as a result of growth in cases of delayed development,
- Vitamin deficiency status and in order to support normal nutrition,
- Health, infection, postoperative Recovery circuit, fatigue, weakness, weight loss, pregnancy and lactation in order to meet the growing need for vitamins and
- Special diet due to vitamin deficiency, is used.

Polivit 30 Dragee

2009-09-12T05:33:00.003-07:00

Indications Polivit

2009-09-12T05:33:00.002-07:00

Nutritional disorders result in children observed growth-growth delay in cases, * Vitamin deficiency status and normal diet in order to support, * the disease, infection, postoperative Recovery circuitry, fatigue, weakness, weight loss, pregnancy and lactation in the vitamin increased the need to meet and * Special diet due to vitamin deficiency, is used.

Polivit Interactions

2009-09-12T05:33:00.001-07:00

Vitamin A, you can create side effects increased with Retinoid containing products. Barbitürat ve antikonvülsanlar, Vitamin D'nin etkisini azaltabilir. Niacin, ganglionik blockers may increase the hypotensive effects. Vitamin B6, Erlich reagent may give inaccurate results in the determination ürobilinojen.

Polivit Side Effects

2009-09-12T05:33:00.000-07:00

In the case of long-term use of excessive doses side effects may occur due hipervitaminoza. Allergic skin rash, mucosal ulcerations and rarely sensation of heat that can be seen, side effects may occur, such as feeling faint.

Megadyn 30 film tablets

2009-09-11T12:14:00.002-07:00

Pharmaceutical Formulation:
As a film-coated tablets Vitamin: Vitamin A 1667 IU Vitamin D3 400 IU Vitamin E 10 IU Vitamin B1 0.90 mg Vitamin B2 1:10 mg Vitamin C 45.0 mg Vitamin B12 Vitamin B6 1:10 mg Biotin 0025 mcg 1:00 mg Folic Acid 0.075 mg Nicotinamide 12.0 mg

Pantothenic Acid as 3:50 mg Minerals: Calcium 25.0 mg Iron Magnesium 2250 mg 31,250 mg 31,250 mg Phosphorus 0250 mg Zinc Copper Manganese 1880 mg 0180 mg Dyestuffs as Red Iron Oxide, Mannitol as a sweetener, Ksilitol,
Sorbitol, Aspartame, smell and taste as a matter of Permaseal 77896-31 Aroma Strawberry, Raspberry Aroma contains 502707/AP 0551.

Warnings and Precautions:
Junior Megadyn Chewing Tablets; hipervitaminoza used in high doses can cause. Containing preparations should not be used in combination with other vitamins.

Side effects:
Junior Megadyn Chewing Tablets; generally well tolerated. Hypersensitivity reactions may occur in sensitive people. When you see an undesired effect please the Ministry of Health Monitoring and Evaluation of Drug Adverse Effects Center (TADMER) 'What's your papers.

Using dose:
Unless otherwise recommended by a doctor, 4 years and over by children chewing tablets a day, preferably in the morning should be taken.

Megadyn 30 film tablets

2009-09-11T12:14:00.001-07:00

Indications Megadyn

2009-09-11T12:14:00.000-07:00

Junior Megadyn Chewing Tablets; growth for children at the age of 12 essential vitamins and 4 minerals and 3 developed oligo-element containing a multivitamin preparations and is Multimineral. Vitamins are substances vital for the organism. Energy, protein, lipid, and nucleic acid metabolism, as well as karbohnidrat amino acid, collagen, and thus the synthesis of neurotransmitter substances such as optimum physical and mental performance are indispensable to perform.

Vitamin A, growth and development of epithelial tissues and plays an important role in the protection. Regulate immune responses and the organism has a protective effect from infection. Vitamin D, calcium and phosphorus absorption, which are the bones of the small intestine regulate the amount of calcium will act as a hormone. Bone-formation and for the health of teeth is required. Vitamin B1, especially important for the metabolism of carbohydrates. Nervous tissue and provides the regularity of heart function. Vitamin B2, has a role in the body's energy production.

Nicotinamide in the body serves as a coenzyme in many metabolic reactions. Especially the cardiovascular system, gastrointestinal system and is important for skin health. Vitamin B6, especially important for protein metabolism. Biotin, leather and leather attachments (hair, nail) is important for development. Vitamin B12 and folic acid, vital for the body cells is catalyzed reaction of many.

Bone marrow cells are experiencing rapid change in particular, such as the gastrointestinal tract has an important role in body tissue. Vitamin C, collagen, osteoid tissue and is helpful to the formation of dentin. Therefore, teeth and bone formation in the body in terms of importance. By strengthening the immune system of the organism shows protective effect against infection. Minerals and oligo-elements, the optimum level of body functions in a healthy way and needed to take place, Junior maddelerdir.Megadyn Chewing Tablets; the body's daily requirement of vitamins and minerals to meet the nutrition support is used.

One-Alpha 1 MCG 10 Bulb

2009-09-10T04:55:00.000-07:00

Drug formula:
Alfacalcidol 1 mcg. / Ampoule Alfacalcidol 2 mcg. / Ampoule

Indications:
The reduction of endogenous production of 1,25-dihydroxyvitamin D3 results emerging diseases are caused by imbalances in calcium metabolism indicated. (Eg, chronic renal failure and osteoporosis)

Warnings and Precautions:
During treatment, serum calcium levels should be monitored regularly. In patients with renal bone disease, phosphate binding agents with kullanılmamısı recommended. Pregnancy and lactation, but by a doctor when necessary should be used in cases

Side Effects:
Hypercalcemia.

Interactions:
Anticonvulsant drugs or other desired effect of barbiturate to be on the use of higher doses may be required.

Using dose:

Starting dose; adults and children 20 kg greater than 1 mcg a day. Daily maintenance dose typically 0.25 to 2 mcg between.

Acceleration can be given after each hemodialysis. Recommended maximum dose for 6 mcg'dır each dialysis, a week should not be exceeded in 12 mcg.

Dose-out: Severe hiperkalsemide curve (loop) diuretics, intravenous fluids and use of corticosteroids may be required.

One-Alpha 1mcg 30 capsules

2009-09-09T04:50:00.003-07:00

Using One-Alpha Dosage

2009-09-09T04:50:00.002-07:00

Starting dose; adults and children 20 kg greater than 1 mcg a day. Daily maintenance dose typically 0.25 to 2 mcg between. Acceleration can be given after each hemodialysis. Recommended maximum dose for 6 mcg'dır each dialysis, a week should not be exceeded in 12 mcg.

Dose-out: Severe hiperkalsemide curve (loop) diuretics, intravenous fluids and use of corticosteroids may be required.

One-Alpha Warnings and precautions

2009-09-09T04:50:00.001-07:00

During treatment, serum calcium levels should be monitored regularly. In patients with renal bone disease, phosphate binding agents with kullanılmamısı recommended. Pregnancy and lactation, but by a doctor when necessary should be used in cases

Using dose Trio

2009-09-08T01:52:00.004-07:00

Reducing the risk of recurrent ulcer Duedenal H. Pylori eradication.
This drug is intended for adults.
The recommended adult dose: 2 times per day with 12 hours (morning and evening) 1 film-coated tablet 500 mg clarithromycin, 1 Micropellet lansoprazole 30 mg capsules and 1 tablet with 1000 mg amoxycillin, 10 or 14 days and should be used. Each drug should be swallowed divisions.
TRIO creatinine clearance 30 ml / min. 'S not recommended for patients who are under.

Dose overflow and Treatment:
In case of overdose patients, doctors immediately, must contact poison control center or emergency services are. Due to the increased intake of all three preparations of a toxicity risk that they are not available pharmacological data.

Clarithromycin
When taken in overdose clarithromycin gastrointestinal symptoms may occur. Allergic reactions accompanying overdose, the stomach can be emptied and supportive treatment should be controlled by applying.
Hemodialysis and peritoneal dialysis does not benefit.

Lansoprazole
Lansoprazolün is no known antidote. Dialysis can not be removed from the body. In case of overdose, symptomatic and supportive treatment should be made.

Amoxicillin
In case of overdose treatment should be interrupted necessary symptomatic and supportive treatment should be applied. Amoxicillin is removed from circulation by hemodialysis.

Storage Conditions:
At room temperature below 25 ° C. Store it in the box. Protect from light and moisture.

Type of Supply and contents of the pack:
Clarithromycin 500 mg film-coated tablets in blister 2 units each, 2 units of lansoprazole 30 mg capsules and 2 Micropellet Amoxicillin 1 g tablets in packages containing 7 and 14 blisterlik.

CHILDREN'S PLACE AND PACKAGING in the U.S. can not please STORAGE.

Trio Interactions

2009-09-08T01:52:00.003-07:00

Clarithromycin
Clinical studies, theophylline and carbamazepine together klaritromisinle implementation result, blood levels of these drugs in moderate but statistically significant (p 0.05) showed an increase.
Other macrolide antibiotics as well as in patients with cytochrome P450 enzyme system which metabolized (eg, warfarin, ergot alkaloids, triazolam, midazolam, lovastatin, dizopiramid, phenytoin, and cyclosporine) use of clarithromycin with drugs, other drugs that increase serum levels may cause.
HMG-Co-A reductase inhibitors clarithromycin, lovastatin and simvastatin and rhabdomyolysis were observed with the implementation.

In patients with combined clarithromycin and digoksini elevated serum digoxin concentrations have been reported. Serum digoxin levels should be considered controlling.
HIV-infected adults with oral clarithromycin and zidovudine continuous implementation zidovudinin can lead to a decrease in steady-state level. Such a reaction has not been reported in children.

When used with ritonavir, clarithromycin, clarithromycin may increase plasma concentrations significantly. The side effects of clarithromycin (diarrhea, nausea, indigestion) growth occurs. Patients with normal renal function when using ritonavir, clarithromycin receives dose is not necessary to make changes. However, creatinine clearance 30-60 ml / min. In patients with clarithromycin dose by 50%, creatinine clearance 30 ml / min. 's should be reduced below 75% of patients. Clarithromycin in patients with renal function should be monitored using ritonavir. 1 g / day at higher doses of clarithromycin and ritonavir should not be applied.

Lansoprazole
Lansoprazole cytochrome P450 enzyme system, especially with CYP3A and CYP2C19 izozimleri Although metobolize done in healthy volunteers> man in studies using the same system warfarin, antipyrine, indomethacin, aspirin, ibuprofen, phenytoin, prednisolone, propranolol, aluminum-magnesium hydroxide or diazepam with clinical antiasidleri as did not reveal an important interaction. Lansoprazolün, together with the use of theophylline, theophylline clearance minor (10%) create an increase. Therefore, the dose of theophylline used in conjunction with necessary adjustments to make during the patient should be monitored closely.

Lansoprazolün with the use of sucralfate, developed delayed absorption and bioavailability lansoprazolün was reduced to 30%. Therefore, lansoprazole, without taking at least 30 minutes before sucralfate should be used. Lansoprazole, aluminum-magnesium hydroxide is applied 1 hour after the antiasid preparations, the statistically significant value Cmax de € has not had an impact.

Lansoprazole inhibits gastric acid secretion because gastric pH is important in terms biyoyararlanımları ketoconazole, ampicillin esters, iron salts, may affect the absorption of drugs such as digoxin.
Lansoprazole when used in conjunction antiasidlerle bioavailability may be reduced. Therefore, at least one hour should be used with antiasidlerle.

Trio 7 Blister Treatment Pack

2009-09-08T01:52:00.002-07:00

Drug formula:
TRIO each blister, each containing 500 mg clarithromycin 2 film-coated tablets, each enteric-coated granules contains lansoprazole 30 mg in 2 pieces Micropellet capsules, 1000 mg each Amoksisiline Amoxicillin Trihydrate equivalent to 2 tablets containing; contains.

Auxiliaries in the trio make up products, titanium dioxide, Tartrazine, Indigo carmine, erythro, Quinoline yellow, yellow iron oxide, Peppermint flavoring, sugar, Sodium Cyclamate and Sodium sakkarin'dir.

Indications:
H.pylori infection and duodenal ulcer disease TRIO (active or one year in patients with a history of duodenal ulcer) is indicated for the treatment. H.pylori eradication reduces the risk of duodenal ulcer recurrence.

Trio Side effects

2009-09-08T01:52:00.001-07:00

Make up the trio of drugs used in triple therapy, the most frequent (> 3%) adverse effects are:
Adverse Effects triple therapy n = 138 (%)
Diarrhea 7.0
Ties Between 6.0
Tad Alma Disorder 5.0

Other side effects seen with triple therapy (3%) are as follows:
Body System: Abdominal pain;
Digestive System: Dark feces, dry mouth, thirst sensation, glosit, rectal itching, nausea, oral monilyazis, stomatitis, tongue color change, language dysfunction, vomiting;
skeletal-Muscle System: myalgia;
Nervous System: Confusion, dizziness;
Respiratory System: Respiratory disorders;
Skin and related structures: skin reactions;
Urogenital System: Vaginitis, vaginal monilyazis.

Clarithromycin
Observed in clinical studies, the majority of mild and transient side effects such as gastrointestinal side effects than the classical macrolides are less common. Drug due to side effects of treatment leaving patients less than 3%. The majority of side effects observed related to the gastrointestinal tract and, diarrhea, vomiting, abdominal pain, dyspepsia and nausea are. Other side effects, headache, taste change and transient rise in liver enzymes.
Sense of smell with taste disorders often receive change have been reported.
Treatment with clarithromycin in patients with tooth-colored degradation was observed. Discoloration with professional teeth cleaning has been corrected.
Some patients treated with hypoglycemic agents or insulin to be seen as rare cases of hypoglycemia have been reported.
Isolated cases of thrombocytopenia have been reported.
As with other makrolidlerle, rarely with clarithromycin, an increase in liver enzymes and hepatocellular jaundice or jaundice without a watch and / or cholestatic hepatic dysfunction have been reported.
This hepatic dysfunction may be severe and usually reversible. Resulted in very rare cases fatal hepatic failure have been reported and usually serious underlying disease and / or related drugs are used simultaneously.
Applied in clinical studies with omeprazole, clarithromycin and temporary color changes were observed in the language. Orally applied clarithromycin and moderate skin eruption and urticaria, anaphylaxis and Stevens-Johnson Syndrome has been extended to generate the allergic reaction. With oral clarithromycin, anxiety, dizziness, insomnia, bad dreams of, confusion, hallucinations of psychosis, dating back to the central nervous system side effects of the transient have been reported. But the causality relationship could not be detected.
Clarithromycin during treatment, the drug with a hearing loss may be shielded from the middle.
In people with long QT syndrome, the use of erythromycin and clarithromycin, ventricular arrhythmias, including ventricular tachycardia and torsade de pointes "lara can lead were found.
Glosit with clarithromycin treatment, stomatitis and oral monilia have been reported.
Damaged Immune System in Patients Adverse Effects:
Mycobacterial infections for long periods with high doses of clarithromycin treated in patients with damaged immune systems, clarithromycin bağılantılı application that may be adverse effects, or the course of HIV disease, the underlying disease to distinguish from symptoms is often difficult.
Some laboratory tests of patients with a clarithromycin may be taken in error. These are below the major include:
Liver function tests: ALT, AST, GGT, alkaline phosphatase, total bilirubin, LDH is higher than the results might happen, but deviation is below 1%.
Blood: The number of leucocytes is low (below 1% deviation), prothrombin time is high (1% deviation) may occur.
Renal: BUN (4% deviation) and serum creatinine values (below 1% deviation) is high may occur.

Lansoprazole
Lansoprazole is a drug well tolerated. Lansoprazole side effects use of eminent ıile diarrhea or constipation that can be seen, nausea, headache and rash is. During maintenance therapy the most frequent side effect diarrhea. These symptoms are lost in the treatment was discontinued in €. Short-term and long-term treatment in patients treated with lansoprazole in the very rare side effects were observed as follows:
Whole body: Asthenia, candidiasis, chest pain, edema, fever, flu-like syndrome, halitosis, infection, malaise.
Cardiovascular System: Angina, cerebrovascular damage, hypertension / hypotension, myocardial infarction, palpitasyonlar, shock (circulatory disorder), vasodilation.
Digestive System: Anorexia, kardiyospazm, kolelityazis, constipation, dry mouth / thirst, dyspepsia, dysphagia, belching, özofajial stenosis, esophageal ulcer, esophagitis, feçeste color added, flatulence, gastric nodules / fundal secretion polyps, gastroenteritis, gastrointestinal hemorrhage, hematemesis, appetite growth, increase in saliva, melena, rectal hemorrhage, stomatitis, tenesmus, ulcerative colitis.
Endocrine System: Diabetes mellitus, goiter, hyperglycemia / hypoglycemia.
Blood and Lymph System: Anemia, hemolysis.
Metabolic and Nutritional Disorders: Gout, weight gain / loss.
Muscle and skeletal system: arthritis / arthralgia, muscle / skeletal pain, myalgia.
Nervous System: Agitation, amnesia, anxiety, apathy, confusion, depression, dizziness / syncope, hallucinations, hemiplegia, hostility, libido decreased, nervousness, paresthesia, thinking disorders.
Respiratory Systems: Asthma, bronchitis, cough increased, dyspnea, epistaxis, hemoptysis, hiccups, pneumonia, upper respiratory inflammation / infection.
Skin and related structures: Acne, alopecia, itching, rash, urticaria.
Organs of special senses: Blurred vision, deafness, eye pain, otitis media, taste disturbances, tinnitus, decrease in visual field.
Urogenital System: Menstrüel disorders, albüminüri, breast growth / gynecomastia, breast tenderness, glukozüri, hematuria, impotens, kidney stone.
Changes in Laboratory Values: Liver function test abnormalities in AST and ALT increase, creatinine, alkaline phosphatase, globulin, and GGTP levels increase bilirubinemi, eosinophilia, hiperlipemi, electrolytes and cholesterol levels increase / decrease, glucocorticoids, and LDH increase, platelet increase / decrease / irregularities, gastrin levels increased.

Amoxicillin
Gastrointestinal: nausea, vomiting, diarrhea.
Hypersensitivity reactions: Erythematous rash makülopopüler and üritiker. Urticaria and other skin rashes and serum sickness-like reactions, antihistamine, and if necessary can be controlled with systemic corticosteroid application. In case of reactions on this type of treatment interruption is appropriate.
Liver: a slight increase in AST have been reported although the clinical significance is unknown.
Blood and lymphatic system: anemia, thrombocytopenia, thrombocytopenic purpura, eosinophilia, leukopenia and agranulocytosis have been reported. These symptoms usually disappear when treatment is interrupted.
Factors that a virus infectious mononükleozda amoxicillin should not be used. Applied to amoxicillin in patients with highly infectious mononükleozlu skin rash has been reported.

CONSULT YOUR DOCTOR IF AN UNEXPECTED EFFECT ENSUES.

Trio Warnings and Precautions

2009-09-08T01:52:00.000-07:00

FORMS USED IN THE PROPOSED ONLY AND TRIO SET FORTH ENDİKASYONDA should. THIS PACKAGE THE PREPARATION of the COMBINATION OR SEPARATE SEPARATE ŞEKLİNDE OTHER TREATMENTS FOR should not.

The treatment of mycotic organisms and bacterial pathogens süperenfeksiyon risk may occur. In such cases, TRIO and appropriate treatment should be implemented immediately cut must be passed.

Clarithromycin

Including with the use of nearly all antibacterial macrolides, slightly ranging from life-threatening level of violence can be seen in pseudomembranous colitis. Therefore the use of an anti-bacterial diarrhea seen in patients following this possibility should be kept in mind. Changes in bowel flora and Antibacterials treatment with Clostridium species has led to the over-produced. Clostridium difficile antibiotic-related enterocolitis research of shows due to a toxin produced. Mild cases of pseudomembranous enterocolitis is generally correct medication is interrupted.

Moderate and severe cases, fluid and electrolyte balance in supply, protein supplements and Clostridium difficile 'versus treatment with an effective antibacterial may be required. Mainly through the liver and kidneys clarithromycin and is excreted. Normal liver function, kidney function, but the parties are corrupted in the dose adjustment required. However, in severe renal dysfunction (liver function, without taking into account) or extended between-dose or the dose should be reduced. Among the macrolide antibiotic clarithromycin group, the other may be cross-resistance should be kept in mind. In combination with hypersensitivity reactions may occur due to tartrazine lake.

Lansoprazole

Lansoprazole is metabolized through after the main bile is excreted. Therefore, the pharmacokinetic profile of the drug, as well as elderly uygulanımında, from moderate to severe hepatic impairment can be affected. Patients with hepatic dysfunction, caution should be given lansoprazole. Severe hepatic failure who must not be used daily doses greater than 30 mg.

Tmax and AUC in the elderly (the area under the curve) values are solid young 2. In elderly patients with hepatic impairment should be carefully used. Symptomatic response to therapy with lansoprazole, gastric tumor does not mean you do not have. Gastric ulcer is suspected should be investigated whether a case was malignant, because the treatment, symptoms can delay diagnosis revised.

Amoxicillin

Penicillin therapy in patients with serious or even fatal anaphylactoid type hypersensitivity reactions have been reported. This type of reaction, especially in people with multiple allergen sensitivity and parenteral, in practice, is seen more frequently than oral application. Hypersensitivity to penicillin treatment is applied to people who are sefalosporinlerle severe hypersensitivity reactions can occur have been reported.

Before starting treatment penicillin penicillin, cephalosporins and other allergens whether the reaction against the pre-awareness should be thoroughly question. Emergency treatment with adrenaline for severe anaphylactoid reactions is essential. According indication of oxygen and i.v. should be given steroids, airway should be kept open, if necessary, intubation should be applied. Long-term treatment as well as all powerful drugs hematopoietic system, kidney and liver function should be monitored at regular intervals. Bacterial pathogens during treatment (entorobakter, psödomonas) and mushrooms with (Candida) süperenfeksiyon possibility should not be forgotten. In such a case should be cut and the appropriate drug treatment should be initiated.

Use in Pregnancy and Lactation Period:

Pregnancy Category C.. Adequate and controlled studies of the trio made hamilelelerde are not available. Only the potential benefit of TRIO in pregnant women, babies in situations where the potential risk should be used more (see Warnings-Measures Department).
Passes into breast milk in very low amounts of amoxicillin. Pass into breast milk is not known whether clarithromycin. Many drugs pass into breast milk and should be kept in mind that this possibility should be careful.

Influence and determine the safety those Lansoprazolün breastfeeding should not be used.
Potential for serious adverse effects in breastfed infants in mind, breast-feeding mothers to stop breastfeeding in the TRIO treatment or decisions about treatment benefits the mother by taking into consideration should be given.

Use in children: pediatric patients infected with H.pylori trio's safety and effectiveness could not be proven.
(Contraindications / Warnings Precautions section-see).
Use in the elderly: Elderly patients may be asymptomatic renal and hepatic dysfunction. This group of patients should be careful when using the Trio.

Glynose 100mg 60 tablets

2009-09-07T06:29:00.005-07:00

Drug formula:
Each tablet 50 mg as active substance. Acarbose contains.

Indications:
Used with diet in the treatment of diabetes mellitus.

Using dose:

It depends on each individual event and tolerance dose should be adjusted by the physician. Otherwise advised by doctors not to dose is as follows: In the beginning Acarbose 3x50 mg / day, then Acarbose 3x100 mg / day. Increasing the dose of Acarbose up to a maximum of 3x200 mg may be required. Dose 4-8 weeks later, patients in advanced stages of treatment can be increased if they give insufficient clinical response. Despite strict diet if you develop discomfort complaints, and if necessary the dose should not be increased more than an amount should be reduced.

The average dose of 300 mg Acarbose / day 'roll (Glynose 50: 3x2 tablet / day or Glynose 100: 3x1 tablets / day). Should be swallowed whole with a little liquid before meals Acarbose or during the first bite of food should be chewed with. Pediatric use: effectiveness and safety in children has not been identified. Senior citizens (65 years): There is no need to adjust the dose. Hepatic impairment: in patients with previously impaired hepatic function, dosage adjustment is required. AND TREATMENT Overdosage: Glynose, carbohydrates (polysaccharides, oligosaccharides, or disakkaritler) containing beverages and / or food is taken in combination with an overdose, meteorizm, can cause gas and diarrhea. Regardless of food taken an overdose case Glynose excessive intestinal symptoms improbable. In case of overdose patients for a period of 4-6 hours of carbohydrates (polysaccharides, oligosaccharides and disakkaritler) containing foods and beverages should not be given.

Thurs Price:
Drug Barcode * 8699514013938 *
Drug Price 18:02 YTL
Issuance prescription.

Interactions Glynose 100mg

2009-09-07T06:29:00.004-07:00

Glynose during treatment with the colon as a result of an increase in carbohydrate fermentasyonunda sucrose and sucrose containing foods often cause abdominal discomfort or diarrhea. Glynose antihiperglisemik effect, but does not create hypoglycemia. If Glynose, sulfonylurea or metformin, and insulin-containing drugs is recommended in addition, blood glucose levels fall to a range to prevent hypoglycemic sulfonylurea, metformin, or insulin dose reduction is required as appropriate. If you develop acute hypoglycemia, during Acarbose treatment sukrozun, fructose and glucose more slowly as the pieces should be kept in mind.

Therefore, rapid correction of hypoglycemia is not suitable for sucrose and glucose should be used. Glynose'un digoxin, nifedipine, propranolol, or pharmacokinetic or pharmacodynamic ranitidin'in has no effect on any. Some medicines cause the blood glucose hyperglycaemic can lead to loss of control. These drugs; tiazidler and other diuretics, corticosteroids, fenotiazin, thyroid products, estrogens, oral contraceptives, phenytoin, nicotinic acid, sympathomimetics, calcium channel blockers, and Isoniazid.

These drugs are given to a patient Glynose field of blood glucose should be monitored more carefully in terms of loss of control. Combination with sulfonylureas or insulin Glynose in patients receiving the above-mentioned drugs is lost, in terms of symptoms of hypoglycemia should be monitored carefully. Adsorbanlar intestinal and digestive enzymes (amylase, Pancreatin) and therefore may reduce the effect akarbozun should not be taken together.

Glynose 100mg side Etkikeri

2009-09-07T06:29:00.003-07:00

Very often as an increase in gas and bowel sounds, diarrhea and often abdominal pain and vomiting are rare. This can be serious gastrointestinal symptoms and bowel blockage or other symptoms can be confused with. Recommended intestinal side effects diabetic diet is not fit to intensify. Diabetic diet-related disease symptoms occurs in the case has been accepted, the doctor should be consulted and the dose should be reduced temporarily or permanently.

The recommended daily 150 to 300 mg / day dose in patients receiving Acarbose rarely, clinically significantly abnormal liver function tests were found (3 times the normal upper limit). Observed during treatment with Acarbose may be temporary abnormal values (see warnings and precautions). Very rarely, rash, erythema, and urticaria ekzantem dependent hypersensitivity skin reactions, such as was seen. Very rarely, edema was seen. Very rarely, jaundice and / or hepatitis and associated liver damage have been reported. CONSULT YOUR DOCTOR IF AN UNEXPECTED EFFECT ENSUES.

Glynose 100mg Warnings and Precautions

2009-09-07T06:29:00.001-07:00

Using a full commitment to Acarbose diabetic diet is mandatory. Regularly consult with physicians from the use of Acarbose should not be cut, this can cause an increase in blood glukozunda. Only in patients under dietary treatment Acarbose does not cause hypoglycemia. Hypoglycemia during treatment Glynose development, use of insulin or sulfonylurea or metformin in patients may occur. In this case the patient is not sucrose, glucose should be given. High doses of asymptomatic elevations of liver enzymes rarely be seen.

Therefore, the first treatment 6 to 12 in liver enzymes should be monitored. Treatment is interrupted can be evaluated in patients Glynose the back of these changes was seen. In patients with renal failure there are no adequate studies, the use should not be recommended. Use in Pregnancy and Lactation: Pregnancy Category B.. Regarding use in pregnant women is not enough information, Glynose should not be used during pregnancy. Radioactive marked as milch Acarbose was given to rats, small amounts of radioactivity were found in milk. There is no sufficient evidence in humans in this regard. However, the drug affects the baby milk seen in, in principle, be given to the mother during breast-feeding is not recommended.

Using dose Asidal

2009-09-06T01:04:00.002-07:00

Otherwise recommended by your doctor unless a day, 4 times (20-60 minutes after meals and before bedtime) 1-4 tablets are taken be violated.
Used within 24 hours and the maximum dose should not exceed tanlet number 16'yı longer than 2 weeks of treatment sürmemeldir.
Under 12 years should not be used in tablet Asidal.

Asidal 30 chewing tablets

2009-09-06T01:04:00.001-07:00

Drug formula:
Magnesium hydroxide 200 mg Tablet
Tablet 25 mg Simetikon
Dried aluminum hydroxide 200 mg Tablet

Indications:
Asidal tablet, caused by stomach acid fermentation, such as burning and indigestion symptoms such as bloating and gas in the digestive system is connected tedvisinde symptomatic complaints.

Warnings and precautions:
Asidal tablet, oral route is used can affect the absorption of other ilaçaların. In patients with kidney failure a long time to anatasitlerin containing aluminum, aluminum in tissues, depending on accumulation increases the risk of dialysis and dialysis-related ensefalopatisi make osteomalasiyi heavy.

Therefore, caution should be used in chronic dialysis patients. Pregnant and breastfeeding women are not shown Reliability should not be used.

Side effects:

Asidal tablets, can cause diarrhea or konstipasyona. When used in high doses for a long time can cause hipofosfatemiye.

Interactions:
All anatasitler, may affect the absorption of the drugs used. Asidal tablet, indomethacin, fofor, cimetidine, salicylates, beta-blockers, chlorpromazine, tetrasiklinle, diflusinal and may reduce the absorption of isoniazid. Therefore, with Asidal tablet can be used with these drugs for at least hour intervals.

Andazol 200mg 2 tablets

2009-09-05T02:18:00.003-07:00

Drug formula:
One filmtablette; Titandioksid Albendazole 200 mg sodium, and contains SACCHARIN.

Indications:
Albendazole in human nematodes (round wolves) and sestodların (strips) for the treatment of infections caused intestinal bowel helmintiasis of hydatid disease caused granulosus'un Echinococcus (hydatid cyst) treatment

Warnings and Precautions:
Albendazole is metabolized in the liver and kidney are not excreted in the liver, kidney and hematopoietic function should be used with caution in patients, treatment before and during treatment, this function should be monitored.

Andazol price:
Drug Barcode * 8699578090029 *
Drug Price 1.79 YTL
Issuance prescription.

Using dose Andazol

2009-09-05T02:18:00.002-07:00

Daily doses greater than 2 years in adults and children, caused by nematodes is helmentiasiste 1x2 tablet. 2x2 to morning and evening Kisthidatikte tablet (800 mg) for 30 days or 2x5mg/kg accounts apply. After 15 days of treatment, if necessary, can be applied to a cure. 1x2 tablet for 3 days of infection Cestod apply.

Andazol interactions

2009-09-05T02:18:00.001-07:00

Methimazole, a strong inhibitor of the enzyme sulfoksidaz Albendazole. May lead to decreased levels Plasmada Albendazole sulfoksid. With the same enzymes as they are metabolized chlorpromazine and Fenbendazol Albendazole plasmada may lead to the decrease in concentration sulfoksid.

Chloramphenicol, erythromycin, Hekzobarbital, Nalidiksik acid inhibits cytochrome P-450 system, they can prevent the construction sulfoksid Albendazole indirectly. Deksametason, production increases and sulfoksid Albendazole can increase plasma concentrations.

Andazol side effects

2009-09-05T02:18:00.000-07:00

Albendazol'e tolerance is very good, the frequency of side effects with placebo are as viewed objects. Toxic effects to be seen.

Reported side effects: nausea, vomiting, abdominal pain, diarrhea, anorexia, constipation, headache, dizziness, lethargy, SGOT, SPGT rise, neutropenia.

Using dose Vogast

2009-08-29T02:46:00.007-07:00

Solution diluted following Zefsolin extent, for external use only.
Dilution with distilled water should be made sure.
• cleaning the wound (cut, scratch); concentration: 1 / 1000 -1/5000 dilution rate: 1/100-1/500
• Skin disinfection; concentration: 1 / 1000 - 1 / 2000 dilution ratio: 1/100-1/200
• as a general disinfectant; concentration: 1 / 1000 - 1 / 8000 dilution ratio: 1/100-1/800
• Bladder washing; concentration: 1 / 5000 - 1 / 20000 dilution rate: 1/500-1/2000
• vaginal washing; concentration: 1 / 2000 - 1 / 5000 dilution ratio: 1/200-1/500
• Breast, nipple hygienic care; concentration: 1/1000-1/2000 dilution rate: 1/100-1/200
• Clothing for sterilization; concentration: 1 / 4000 dilution ratio: 1 / 400
• Surgical instruments disinfection; concentration: 1 / 1000 dilution ratio: 1 / 1
• Tools to be used for the protection of 0.1% solution of sodium nitrite is added corrosion is prevented.

Micropellet Vogast 30mg capsules

2009-08-29T02:46:00.005-07:00

Drug formula:
Lansoprazole, 30 mg

Indications:
In the treatment of duodenal ulcer.

Side effects:
Externally, the concentration used in a significant adverse effect is seen when yoktur.İstenmeyen Turkish Ministry of Health Monitoring and Evaluation of Drug Adverse Effects Center (TADMER) have reported.

Vogast Interactions

2009-08-29T02:46:00.003-07:00

Zefsolin solution with the following article is cantankerous. Alimümyum, benzilefedrin, 5% boric acid, caramel, sitrit acid ethyl baraben hydrogen paroksit, iodine, kokalin, lanolin, fizostigmin, pilocarpin nitrate (3% or more intense) potansium permanganate, saponin (0.1% -0.5) silicates, silver tuzlari, sodium citrate and tartrate, sodium lorilsulfat, sulfapiridin, sulfatiyazol sodium, synthetic rubber The material, tartaric acid, zinc oxide, zinc sulfate and zinc peeroksit.

Vogast warnings and precautions

2009-08-29T02:46:00.001-07:00

Benzalkonium chloride solution, with a strong solution of soap and lysol kloroksilenol solution containing antiseptic, such as with soap, detergent aniyonik with the solution karıştırılmamalıdır.Kalsium, iron, magnesium, aluminum cation, such as solutions to interact with tap water and not drink distilled water when hazırlanmalıdır.Yanlışlıkla, (toxic dose 1 -- 3 g / day between). The symptoms of poisoning, nausea, vomiting and collapse in the final circuit of the esophagus and stomach komadır.Çözelti primarily local irritation in the intestines makes the channel.

Excessive doses taken after the unrest anxiety, dyspnea, cyanosis, konvilsiyon, zaafiyeti muscle paralysis and respiratory muscles as a result of death, vomiting and gastric lavage görülecektir.Tedavide is applied, then the patients milk, egg whites or soap solution is given. Respiratory oxygen are supported; konvülsüyonlar for the short-acting barbiturates or iv guide carefully before use is dezanpan read carefully.
If you are using drugs certainly inform your doctor or pharmacist

Panto 40mg 28 tablet

2009-08-27T12:34:00.004-07:00

Drug formula:
Each tablet, 40 mg equivalent amount of 45.10 mg Pantoprazole Pantoprazole sodium Dyestuffs: Titanium dioxide, Quinoline yellow

Indications:
Panto 40 mg Enteric Coated Tablets: - Duodenal ulcer, - gastric ulcer, - Middle and severe reflux disease and reflux esophagitis gastroözofajeal indicated.

Panto Dose Using

2009-08-27T12:34:00.003-07:00

Unless otherwise recommended by a doctor, the recommended daily dose of 40 mg (1 enteric-coated tablet) capability. Tablets must not be divided and should not be violated. Panto 40 mg enteric-coated tablets before breakfast, or breakfast during the week is recommended to be taken. Duodenal ulcer: Panto time, a single dose of 40 mg enteric-coated tablets are taken 1 a day. Duodenal ulcers usually cured within 2 weeks.

If you need a two-week treatment more feasible. Erosive esophagitis associated with gastric ulcer and reflux gastroözofajeal: Panto time, a single dose of 40 mg enteric coated tablets 1 a day is given. For the treatment of gastric ulcer and reflux disease gastroözofajeal usually requires a period of 4 weeks. Not respond to treatment in patients with treatment is continued for 4 weeks. Helicobacter pylori eradication: eradication of Helicobacter pylori in the Panto 40 mg Enteric Coated Tablet, 1 or 2 times a day amoxicillin, clarithromycin and metronidazole is used in combination, such as antimikrobiyallerle. And kidney function in patients in the elderly: Dosage adjustment is not required. In patients with hepatic cirrhosis: hepatic metabolism in patients with cirrhosis pantoprazolün to have been affected, one tablet should be taken every other day.

This is a rise in liver enzymes are seen in patients with treatment should be discontinued. Overdosage AND TREATMENT: Symptoms of acute toxicity; hipoaktivite, ataxia and tremordur. In case of overdose, symptomatic and supportive treatment is applied. Pantoprazole largely attributed to proteins that can not be removed by hemodialysis.

Panto Interactions

2009-08-27T12:34:00.002-07:00

Panto 40 mg Enteric Coated Tablets in the cytochrome P450 liver enzyme system to be metabolized, even though this system still is metabolized sisaprid, theophylline, diazepam, warfarin, phenytoin, metoprolol, nifedipine, carbamazepine, or oral kontraseptiflerle Used together, these medicines to make a dose adjustment is required. Pantoprazole given any interaction with antacids was observed. Pantoprazole inhibits gastric acid secretion for a long time because, ketokanazol, ampicillin esters, iron salts, such as bioavailability and absorption of drugs may reduce gastric pH'a connected.

Side effects Panto

2009-08-27T12:34:00.001-07:00

Panto 40 mg Enteric Coated Tablets are generally well tolerated drug. The incidence of side effects are not dose dependent. Rarely during treatment with Pantoprazole skin rash, itching and rash in the form of allergic reactions, headache, dizziness, diarrhea, abdominal pain, bloating, nausea, vomiting, hyperglycemia, insomnia can be seen.

More rarely encountered side effects are: dyspepsia, anxiety, arthralgia, asthenia, back, chest or neck pain, bronchitis, upper respiratory tract infection, urinary tract infection, constipation, hypertonic. In addition, as a very rare for an increase in liver enzymes, hypercholesterolemia, and hyperuricemia have been reported.

Panto Warnings and precautions

2009-08-27T12:34:00.000-07:00

Pantoprazole therapy ease the symptoms of malignant ulcers diagnosed by delayed, gastric ulcer before treatment of malignancy or malignant esophageal disease, the possibility must be removed. Because long-term potential side effects of stomach acid blocking control methods available in terms of endoscopic and radyoskopik found as resistant to treatment with drugs duodenal ulcer, gastric ulcer, moderate and severe reflux esophagitis is used. Children on how to use Pantoprazole is not enough work, pantoprazolün use in children is not recommended. The use of tools and machinery has no effect on the well-known.

Use in pregnancy: Pregnancy Category B in pregnancy with the use Pantoprazole there are no adequate studies, Panto 40 mg Enteric Coated Tablet potential benefit / risk ratio should be used in cases where the excess. Lactation use: Pantoprazolün fully switch to breast milk is unknown, according to the potential benefits of breast-feeding women or breast-feeding of drugs must decide to stop.

Carnitene 1gr 5 bulbs

2009-08-26T07:03:00.004-07:00

Drug formula:
L-Carnitine in each tablet active substance in 1 g of salt, sugar as a sweetener is found.

Indications:
Primary carnitine deficiency, oil storage myopathy due, carnitine deficiency observed in patients who underwent hemodialysis.

Thurs Price:
Drug Barcode * 8699527754361 *
Drug Price 11.74 YTL
Issuance prescription.

Carnitene Warnings and Precautions

2009-08-26T07:03:00.003-07:00

During treatment with the patient's drug Carnitene ® clinical response, vital signs, blood chemistry, plasma and urine carnitine concentrations must be checked periodically and the dosage should be adjusted if necessary. No Mutajenitesi. Does not affect fertility and the fetus. In PREGNANT: Yap was well-controlled studies are not sufficient should be used only when clearly needed. In the composition of human milk, breastfeeding, those that study has found.

"Dialysis implemented or gross inadequacy of pie in patients, elimination pie has not been carried through, the main metabolite (trimethylamine [TMA] and trimethylamine-N-oxide [TMAO]) accumulate in the blood due to high doses of oral formulations in the long-term use is recommended. Such an accumulation, in the urine , the heavy breathing and sweat in a "fish smell" as a condition characterized by pathological causes trimetilaminüriye. This phenomenon does not occur with intravenous administration.

Side effects Carnitene

2009-08-26T07:03:00.002-07:00

Be given by mouth during long Carnitene ® nausea, vomiting, diarrhea, abdominal cramps, mild transient gastrointestinal complaints such as high-dose body odor (fish) have been reported. This drug is generally divided complaints during or after dinner to take food and / or dose reduction may alleviate or may disappear.

Require both oral intravenous levokarnitin field (with or without previous seizure history) can occur in patients with seizures, seizure history before the current ones, increase in frequency and severity of seizures has been reported to be seen.

Using dose Carnitene

2009-08-26T07:03:00.001-07:00

Chewing Tablets ® 1 g Carnitene; In adults, the recommended dose for patients weighing 50 kg a day 2-3 times 1 g (1 tablet) capability. In children, daily doses of 50-100 mg / kg, 3 g per day is too. Daily dose divided into equal parts 3-4 days, 3-4 hours, preferably with a meal is taken during or after dinner in violation. 1 tablet per day for patients who underwent hemodialysis. Treatment to cope with low-dose (1 g in adults, children 50 mg / kg), given the patient's tolerance and to increase the dose according to clinical response is appropriate.

And clinical response to high doses recommended but if foreseen biyoşimik findings should be applied with caution. Cases according to the duration of treatment varies between 1-12 months. In some patients, periodic clinical and lifelong biyoşimik controls should continue to be made. WARNINGS REGARDING USE OF ORAL FORM doctor with Carnitene ® should be used. Drug-related gastrointestinal side effects and recommended to be taken to alleviate and may disappear.

Body odor is typically connected to a high dose and dose reduction are lost. The first week of the treatment of patients tolerate the drug and should be closely monitored after each dose increase. Treatment with L-Carnitine Overdosage and toxicity has not been reported due to overdose. Excessive doses can cause diarrhea. In this case the dose should be reduced and supportive treatment should be applied.

Diameprid 4mg 30 tablets

2009-08-25T04:55:00.004-07:00

Drug formula:
1:00 mg tablet Glimeprid

Indications:
Blood glucose levels alone, diet, physical exercise and weight loss can not be controlled adequately with non-insulin dependent (type II) is used in cases of diabetes.

Contraindications:
Glimeprid, insulin-dependent diabetes (type I diabetes) (for example, previously for the treatment of diabetic ketoacidosis with a history), diabetic ketoasidozun or for the treatment of diabetic coma prekoma or is not. Glimeprid other sülfonilürelere, or help other sulphonamides in patients with hypersensitivity to substances should not be used (risk of hypersensitivity reactions).

In patients with severe liver failure and no experience regarding the use of dialysis patients has not been won. Serious kidney or liver dysfunction in patients with optimal metabolic control right until the Commencement of insulin therapy is recommended.

Pregnancy Category C. pregnancy and lactation. Fetuses to avoid potential risks during pregnancy and should not be taken glimeprid plan to stay pregnant patients should inform their physician. Such patients to insulin therapy should be initiated. Is passed into breast milk to baby Glimeprid damage. Therefore, breast-feeding mothers should not use the glimeprid.

Per. Price:
Barcode medication * 8699633013789 *
Pharmaceutical Price 7.82 YTL
Issuance prescription.

Using a dose Diameprid

2009-08-25T04:55:00.003-07:00

In principle, desirable blood sugar glimeprid'in dosage is adjusted according to the level. Glimeprid dosage, will be sufficient to provide the desired metabolic control should be kept minimal. Initiated by a physician and should be Glimeprid treatment should be monitored. Prescribed times and doses Glimeprid should be taken. For example, errors such as forgetting a dose of receipt of the higher dose to be taken any time after it should not be corrected. If too high a dose or physician has taken an extra dose should be reported immediately. Initial and maintenance doses based on the results of blood and urine checked regularly glukozunun is set to monitoring and urine glucose levels on the treatment of the primary and secondary failure ensures.

Starting dose and dose adjustment usual starting dose, 1 mg once a day glimeprid'dir (should not exceed 2 mg-ROM). Daily dose can be increased if necessary. To monitor blood sugar and should be based on regular increases in stages, such as for example one to two week intervals and the following steps according to the dose of 1 mg - 2 mg - 3 mg - 4 mg - 6 mg and 8 mg should be made in exceptional circumstances. Well-controlled diabetes in patients with diabetes in patients with controlled doses sınırlarıİyi usual dose range from 1 to 4 mg per day glimeprid'dir. Only in some patients higher than 6 mg daily dose may be needed. Dose distribution and dose distribution timing considering the patient's lifestyle should be decided by a physician. Normally a single daily dose is sufficient glimeprid. This is a strong dose immediately before breakfast or not eat-nothing-to be taken immediately before the first main meal is recommended.

After the meal is very important not to jump Glimeprid. Diabetes control improved as the secondary dose adjustment, insulin sensitivity is increased. Therefore, treatment can decrease the need glimeprid progresses. To avoid hypoglycemia in the treatment time, dose reduction or discontinuation glimeprid should be taken into consideration. Dosage adjustment or patient's weight is changed or the patient's life style is changed or hyperglycaemic against hypoglycemia or an increased sensitivity to other factors that may cause occurs (Warning and Precautions see) should be taken into consideration. The duration of treatment as normal Glimeprid treated with long-term treatment.

Other oral blood glucose lowering and other antidiyabetiklerden glimepirid'e transition Glimeprid between agents is not a clear dose relationship. Agents when used in place of this type Glimeprid other daily starting dose of 1 mg. This is another case of the maximum dose of oral blood sugar-lowering agents, even in the transition is applied. Any increase above the initial dose glimeprid dose and dose adjustments must be compatible with.

The effect of blood sugar-lowering agents earlier time and power should be taken into consideration. Drug intake for a while granting that increase the risk of hypoglycemia may be necessary to avoid additive effects. Combination therapy with insulin and insulin Glimeprid combination therapy, in patients with treatment failure can be applied. To begin combination therapy patients, depending on the level of fasting plasma glucose or serum 150 mg / dL should not be over. 1 times the recommended dose glimeprid first main meal to be implemented with 8 mg. Starts with low doses of insulin after fasting blood sugar measurements in accordance with the regular insulin dose adjustment (increasing) can be done on a weekly basis. Glucose and HbA1c levels during maintenance treatment according to the periodic insulin dose adjustment may be necessary. Safety and efficacy in patients under 16 belong to the clinical data is not available. With a sufficient amount of liquid without chewing tablets Glimeprid as a whole must be swallowed.

Diameprid interactions

2009-08-25T04:55:00.002-07:00

Certain other drugs while under treatment Glimeprid area or stop taking blood sugar control may experience changes. Glimeprid obtained by experience and other sulfonylureas known about on the basis of interaction following consideration should be taken into insulin and other oral antidiyabetikler, ACE inhibitors, allopurinol, anabolic steroids and male sex hormones, chloramphenicol, coumarin derivatives, cyclophosphamide, dizopiramid, fenfluramin, fibrates, fluoxetine, Guanethidine, MAO inhibitors, mikonazol, paraaminosalisilik acid, high-dose parenteral pentoxifylline, Phenylbutazone, Azapropazone, Oxyphenbutazone, probenecid, quinolones, salicylates, Sulfinpyrazone, sulphonamides, tetracyclines such as the one received drugs lowering blood sugar may increase and therefore in some cases with hypoglycemia may occur.

Acetazolamide, barbiturates, corticosteroids, diazoksit, diuretics, epinephrine (adrenaline) and other sympathomimetic agents, glucagon, after long-term laxative use, high doses of nicotinic acid, Estrogens and progestojenler, fenotiazinler, phenytoin, rifampin, thyroid hormone drugs, such as blood sugar when taken one lowering blood sugar levels may increase to the weakening. H2 receptor antagonists, blood sugar-lowering effects of clonidine and rezerpin or weakening of the increase may cause. Beta-blockers reduce glucose tolerance. Diabetes mellitus and metabolic control in patients with this condition may cause deterioration. Beta-blockers, clonidine, and Guanethidine as rezerpin under the influence of drugs sempatolitik, against hypoglycemia may be reduced or no symptoms of adrenergic regulation may not be. Both chronic and acute alcohol intake, blood sugar-lowering effect glimeprid'in unpredictable manner may increase or may weaken. The effect of coumarin derivatives may increase or decrease.

Diameprid side effects

2009-08-25T04:55:00.001-07:00

Acquired experience with Glimeprid and other information based on the following sülfonilürelere adverse events should be considered. Blood sugar lowering effect Glimeprid'in hypoglycemia as a result of hypoglycemia may occur and also may take longer.

Among the possible symptoms of hypoglycemia headache, extreme hunger, nausea, vomiting, weakness, drowsiness, sleep disturbances, irritability, aggression, concentration disorders, disturbance in attention and reaction, depression, confusion, speech disorders, aphasia, visual disturbances, tremor, paraziler, sensory disorders, dizziness, weakness, otokontrol loss, delirium, cerebral convulsions, somnolence, coma, and where loss of consciousness can be considered bradycardia.

In addition, sweating, moist skin, anxiety, tachycardia, angina pectoris and cardiac arrhythmias such as adrenergic symptoms may be against the regulations. The clinical picture of severe hypoglycemic attacks, stroke may be similar to the table. Hypoglycemia is corrected, hypoglycemia symptoms almost always disappears. Especially at the beginning of eye treatment, depending on changes in blood sugar levels may be temporary visual impairment. Sometimes the digestive system, nausea, vomiting, or feeling of fullness epigastriumda pressure, symptoms such as abdominal pain and diarrhea may occur.

In rare cases may increase liver enzyme levels, liver dysfunction (eg, cholestasis and jaundice) and possibly hepatitis resulting in liver failure may develop. Significant changes may occur in the statements of cancan. Rarely, trombopeni, in rare cases, leukopenia, hemolytic anemia or eritrositopeni eg, granulocytopenia, agranulocytosis and pancytopenia (depending miyelosupresyona) may develop. Other in some cases, pruritus, urticaria, or in the form of rashes or allergic reactions may occur psödoalerjik.

Such reactions are mild but can be serious and sometimes dyspnea and blood pressure can progress to shock, it can affect in the fall. Urticaria are seen physicians should be informed immediately. In rare cases, allergic vasculitis, and skin hypersensitivity to light, a fall in serum sodium concentration can be seen.

Severe hypoglycemia, blood in the statements of certain changes, or psödoalerjik severe allergic reactions or liver failure, such as adverse effects under certain conditions, life-threatening sudden become or severe reactions occurs first physician tell whether the physician's knowledge of the drug outside should not be used.

Diameprid warnings and precautions

2009-08-25T04:55:00.000-07:00

Optimal blood sugar control to ensure the correct nutrition, regular and adequate physical exercise and weight loss if necessary, at least as important as regular intake is glimeprid. Not sufficiently reduce blood sugar (hyperglycemia) clinical symptoms, increased frequency of urination, excessive thirst, dry mouth and dry skin is like. Getting started with the treatment of patients glimeprid'in effects, risks, diet and physical exercise should be informed about the application effect. In the early weeks of treatment may have an increased risk of hypoglycemia, and especially careful monitoring is required during this period. The factors supporting hypoglycemia
- The patient's reluctance to communicate or (more often in elderly patients) failure,
- Diet failure, irregular meal intervals and missed meals,
- Imbalance between physical exercise and carbohydrate intake,
- Changes in diet,
- Alcohol consumption, especially in conjunction with missed meals,
- Renal dysfunction,
- Serious liver dysfunction,
- Glimeprid overdose,
- Carbohydrate metabolism that affect the endocrine system disorders, certain not been compensated,
- Some medications used in conjunction with which drug interactions (see drug interactions).
This type of hypoglycemic attacks, especially factors and require careful follow-up physician should be informed about them. If you have risk factors for this type of hypoglycemia, or glimeprid dosing may be necessary to rearrange the whole treatment. Another disease occurs during treatment or the patient's life style is changed, the treatment may need to be revised.

Symptoms of hypoglycemia in the elderly and in patients with autonomic neuropathy or beta-blockers, clonidine, rezerpin, Guanethidine or other drugs with sempatolitik treated patients may be lighter or no, however. Hypoglycemia, with carbohydrate intake (glucose or sugar, for example, lump sugar, sweetened fruit juice and sweetened tea in the form of) almost always can be controlled in the desired format.

To this end, patients must always carry with them a minimum of 20 grams of glucose. To avoid complications of other people may need help. Artificial sweeteners are ineffective in controlling hypoglycemia. Other successful measures taken in the beginning as it is known sülfonilürelerden despite repeated hypoglycemia may occur.

Therefore, under the constant eye must be kept. Severe hypoglycemia, in addition to emergency treatment, followed by a physician and in some cases require hospital treatment. Treated by different doctors when necessary eg after an accident, hospitalization, while on holiday, such as disease status and previous treatment of diabetes patients must inform the doctor about.

Privileged in cases of stress (eg trauma, surgery, fever infections) of blood sugar control may become corrupted and may need to start insulin temporarily. Glimeprid during treatment, blood and urine glucose levels should be checked regularly, in addition to the rate of glycated hemoglobin should be monitored. Getting started with treatment, or treatment, especially after changing or not taken regularly hypo or hyperglycaemic depending glimeprid attention and reaction may be corrupted. For example, may affect the use of vehicles or machinery.

Butopan 6 Ampule 20mg/ml

2009-08-22T07:00:00.003-07:00

Drug formula:
Dragee br Skoplamin butyl 0.01g
0:02 br g Skoplamin butyl Bulb 1

Indications:
Stomach, duedonum, thin and thick bowel, ureter, bladder and bile ducts of the spasm, and spastic pain in colic, spastic dismenore, posttoperatif nausea and vomiting in the treatment, the birth of my sleeve in the elimination of spasm and placenta are removed to facilitate; endoscopic examination, the small ürolojik and spasm of gynecologic müdahelelerde to prevent.

Side Effects:
Dry mouth, konstipasyon, tenesmus, tachycardia, seen in the dimness, midriasis, dry mucous membranes and skin, anhidrosis, sleepiness, ortostatik hypotension, skin rashes, the hives, weakness, impotens, blushing percent.

Butopan Dose Adjustment

2009-08-22T07:00:00.002-07:00

Dragee Butopan: older children over the age of 6, and 3-5 times a day for 1-2 doses mutad is coated tablet. Children between the ages of 6 to 1ile doses 3-5 times per day is 1 coated tablet.
Butopan Ampule: intramusküler or in the form of intravenous injection is used. 1 bulb at a time in large doses mutad, 1-4 ampuldur day. Injection should be made in 6-8 hours.