Ranitidine + Drotaverine Pharmacology

Ranitidine + Drotaverine

About Ranitidine + Drotaverine
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Mechanism of Action of Ranitidine + Drotaverine
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Pharmacokinets of Ranitidine + Drotaverine
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Onset of Action for Ranitidine + Drotaverine
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Duration of Action for Ranitidine + Drotaverine
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Half Life of Ranitidine + Drotaverine
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Side Effects of Ranitidine + Drotaverine
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Contra-indications of Ranitidine + Drotaverine
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Special Precautions while taking Ranitidine + Drotaverine
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Pregnancy Related Information
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Old Age Related Information
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Breast Feeding Related Information
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Children Related Information
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Indications for Ranitidine + Drotaverine
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Interactions for Ranitidine + Drotaverine
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Typical Dosage for Ranitidine + Drotaverine
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Schedule of Ranitidine + Drotaverine
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Storage Requirements for Ranitidine + Drotaverine
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Effects of Missed Dosage of Ranitidine + Drotaverine
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Effects of Overdose of Ranitidine + Drotaverine
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Ranitidine

About Ranitidine
A histamine H2-receptor antagonist, Furan derivative, Anti-secretory G.I agent,Anti ulcer.
Mechanism of Action of Ranitidine
Ranitidine is a H2 (Histamine) receptor antagonist. Histamine is the most potent stimulus of acid secretion and acts as the common mediator. H2 receptor is a G-protein coupled receptor. It induces adenylate cyclase which converts ATP to cyclic AMP. This cyclic AMP acts on proton pump and exchange extracellular potassium ion for intracellular hydrogen ion across the parietal cell membrane. Ranitidine reversibly competes with Histamine for binding to H2 receptors on the parietal cells and predominantly inhibits basal acid secretion.
Anaesthetic adjuncts: It is used in patients undergoing prolonged operations, caesarian section,obese patients those are at increased risk of gastric regurgitation and aspiration pneumonia. It raises pH of gastric juice and also reduces its volume and thus chances of regurgitation. It is now routinely used before prolonged surgery.
Pharmacokinets of Ranitidine
Absorption: Ranitidine is 50 % absorbed after oral administration. Distribution: Distributed mainly to body tissues in unbound form. Metabolism: Ranitidine undergoes metabolism in the liver. Excretion: It is excreted mainly in urine and in the faeces.
Onset of Action for Ranitidine
60 minutes
Duration of Action for Ranitidine
13hours
Half Life of Ranitidine
1.6- 2.4 hours
Side Effects of Ranitidine
1. Headache
2. Dizziness
3. Constipation
4. Vertigo
5. Confusion
6. Rash
7. Blurred vision
8. Thrombocytopenia
9. Leukopenia
Contra-indications of Ranitidine
1. Hypersensitivity to Ranitidine
Special Precautions while taking Ranitidine
1. Hepatic impairment
2. Renal impairment
3. Acute Porphyria
Pregnancy Related Information
Use with caution
Old Age Related Information
Use with caution
Breast Feeding Related Information
Use with caution
Children Related Information
Use with caution
NEONATES: Contraindicated
Indications for Ranitidine
1. Duodenal ulcer
2. Benign gastric ulcer
3. Zollinger- Ellison syndrome
4. Gastroesophageal reflux
5. Acid indigestion
6. Heart burn
7. Sour stomach
8. Stress ulcers
9. Oesophagitis
10.Preanaesthetic medication
Interactions for Ranitidine
Antacids: Ranitidine absorption may be decreased.
Diazepam: Efficacy of diazepam decreased.
Procainamide: Renal clearance of procainamide decreased.
Sulfonylureas: Hypoglycemic effects of glipizide enhanced.
Theophyllines: Increased efficacy of theophyllines with possible toxicity.
Warfarin: Increased hypoprothrombinemic effects.
Lab tests: False positive tests for urine proteins with multistix may occur.
Typical Dosage for Ranitidine
Adult: 300mg / day
Duodenal ulcer, benign gastric ulcer: 300 mg /day as single dose at bed time or in 2 divided dose (morning and bed time) for minimum of 4 weeks.
Maintenance dose: 150 mg / day at bed time.
Zollinger- Ellison syndrome: 300 - 450 mg / day in 2 - 3 divided doses; dose can be increased if necessary to a maximum up to 6g / day .
Gastroesophageal reflux: 300 mg / day as single dose at bed time or in 2 divided doses (morning and bed time) for maximum 2 months. In severe conditions dose can be increased to 600 mg / day in 4 divided doses for 3 months
Acid indigestion, Heart burn, Sour stomach: Dose: 75 mg once daily to a maximum up to 150 mg / day.
Oesophagitis: 150 mg/ day.
Dyspepsia: 75 - 300 mg / day depending on the severity of disease.
PAM: 150mg given night and in the morning before surgical procedures.
Children:
Duodenal ulcer, benign gastric ulcer: 4 - 8 mg / kg body weight / day in 2 divided doses.
Maximum dose: 300 mg / day
Schedule of Ranitidine
H
Storage Requirements for Ranitidine
Store at 15 - 30 degree C in a tightly closed container. Protect from light.
Effects of Missed Dosage of Ranitidine
Take the missed dose as soon as noticed and if it is the time for next dose then skip the missed dose. Continue the regular schedule. Do not double the dose.
Effects of Overdose of Ranitidine
Give supportive measures and symptomatic treatment. Drug can be removed from the body by inducing emesis and or by gastric lavage. Activated charcoal is given to reduce the absorption of the drug. Haemodialysis can be done if necessary.

Drotaverine

About Drotaverine
Drotaverine is an effective spasmolytic drug.
Mechanism of Action of Drotaverine
Drotaverine has spasmolytic and vasodilating action. It exerts its action by inhibiting phosphodiesterase enzyme IV. This will leads to a decrease in cyclic AMP level and reduction in calcium ions (Ca2+). The reduction of calcium ions will dilates the unstipped muscles and blood vessels strongly and relieves spasm of smooth muscles.
Pharmacokinets of Drotaverine
Absorption: Drotaverine is rapidly absorbed after oral administration.
Distribution: It is widely distributed in protein bound form.
Metabolism: Extensively metabolised in the liver.
Excretion: It is excreted mainly with the bile.
Onset of Action for Drotaverine
30 minutes
Duration of Action for Drotaverine
4 hours.
Half Life of Drotaverine
7 - 12 hours
Side Effects of Drotaverine
1.Hypotension
2.Headache
3.Tachycardia
4.Nausea
5.Vertigo
Contra-indications of Drotaverine
1.Hypersensitivity to Drotaverine
2.Severe renal impairment
3.Severe hepatic impairment
4.Severe cardiac impairment
Special Precautions while taking Drotaverine
1. Renal impairment
2. Hepatic impairment
3. Cardiac impairment.
Pregnancy Related Information
Use with caution
Old Age Related Information
Use with caution
Breast Feeding Related Information
Use with caution
Children Related Information
Use with caution
NEONATES: contraindicated
Indications for Drotaverine
1.Smooth muscle spasm
2.Gastrointestinal colic pain
3.Renal colic pain
4.Dysmenorrhoea
5.Uterine neck spasm
6.Post MTP(Medical termination of pregnancy)
7.Post D&C(Dilatation and curettage)
8.Post surgical spasm
9.Irritable bowel syndrome
Interactions for Drotaverine
N/A
Typical Dosage for Drotaverine
Adult:
Oral: 120 - 240 mg / day in 3 divided doses.
Children: 60 - 120 mg / day in 3 divided doses, dose is depending upon the age of the patient.
Parenteral (IM)
Induction of labour: 40 mg every 2 hours, maximum 3 doses.

Schedule of Drotaverine
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Storage Requirements for Drotaverine
Store in a cool dry place. Protect from heat and light.
Keep out of the reach of children
Effects of Missed Dosage of Drotaverine
Take the missed dose as soon as noticed and if it is the time for next dose then skip the missed dose. Continue the regular schedule. Do not double the dose.
Effects of Overdose of Drotaverine
Give supportive measures and symptomatic treatment.

Home Delivery for Ranitidine + Drotaverine in Your City

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Ranitidine + Drotaverine is a generic medicine name and there are several brands available for it. Some of the brands for ranitidine + drotaverine might be better known than ranitidine + drotaverine itself. If the pharmacy that's willing to deliver medicines to your home doesn't have ranitidine + drotaverine in stock, you can ask for one of the branded alternatives for ranitidine + drotaverine.