Inhouse product
Indications
Voniza is indicated
for:
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Vonoprazan is a
potassium competitive acid blocker (P-CAB) and does not require activation by
acid. It inhibits H+, K+-ATPase in a
reversible and potassium-competitive manner. Vonoprazan has a strong basicity
and resides on the acid production site of gastric parietal cells for a long
time, thereby inhibiting gastric acid production. Vonoprazan exerts a strong
inhibitory effect on formation of mucosal damage in upper part of the
gastrointestinal tract.
Dosage
Gastric ulcer and
duodenal ulcer: The usual adult dose
for oral use is 20 mg of Vonoprazan administered orally once daily an 8-week
treatment for gastric ulcer and a 6-week treatment for duodenal ulcer.
Reflux esophagitis: The usual adult dose for oral use is 20 mg
of Vonoprazan administered once daily for a total of 4 weeks of treatment. If
that dosing proves insufficient, the administration should be extended, but for
no longer than 8 weeks of treatment.
For the maintenance therapy of reflux esophagitis showing recurrence and
recrudescence, the dose for oral use is 10mg of Vonoprazan once daily. However,
when the efficacy is inadequate, the dosage may be increase up to 20 mg of
Vonoprazan once daily.
Prevention of
recurrence of gastric or duodenal ulcer during low-dose aspirin administration: The usual adult dose is one tablet of 10 mg
of Vonoprazan administered orally once daily.
Prevention of
recurrence of gastric or duodenal ulcer during non-steroidal anti-inflammatory
drug (NSAID): administration The
usual adult dose is one tablet of 10 mg of Vonoprazan administered orally once
daily.
Adjunct to
Helicobacter pylori eradication: For adults, the following three-drug regimen should be
administered orally at the same time twice daily for seven days: 20 mg of
Vonoprazan, 750 mg of amoxicillin hydrate and 200 mg of clarithromycin. The
dose of clarithromycin may be increased as clinically warranted. However,
dosage should not exceed 400 mg twice daily.
If Helicobacter pylori eradication with a three-drug regimen comprising a
proton pump inhibitor, amoxicillin hydrate and clarithromycin has been
unsuccessful, as an alternative treatment, adults should be administered the
following three drugs orally twice daily for seven days: 20 mg of Vonoprazan,
750 mg of amoxicillin hydrate and 250 mg of metronidazole.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Administration
Vonoprazan can be
taken without regard to food or timing of food.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Contraindications
Vonoprazan is
contraindicated in:
Side Effects
Following side effects
have been reported with the use of Voniza: Diarrhea, constipation, drug
hypersensitivity (including anaphylactic shock), drug eruption, urticaria,
hepatotoxicity, jaundice, rash, nausea, abdominal distension, gamma-glutamyl
transferase increased, AST increased, Liver function test abnormal, ALT
increased, ALP increased, LDH increased, y-GPT increased, edema and
eosinophilia
Pregnancy & Lactation
Vonoprazan should be
used in pregnant women or women having possibility of being pregnant only if
the expected therapeutic benefit is thought to outweigh any possible risk. It
is advisable to avoid the administration of Vonoprazan to nursing mothers.
However, when the administration is indispensable, nursing should be
discontinued.
Precautions & Warnings
At the treatment, the
course of the disease should closely be observed and the minimum therapeutic
necessity should be used according to the disease condition. In the long-term,
treatment with Voniza, close observation by such means as endoscopy should be
made.
In the maintenance of healing of reflux esophagitis, Voniza should be
administered only to the patients who repeat recurrence and recrudescence of
the condition. Administration to the patients who do not necessitate
maintenance of healing should be avoided.
When the healing is maintained over a long period and when there is no risk of
recurrence, the dose reduction to a dose of 10mg from a dose 20mg, or
suspension of administration should be considered.
Use in Special Populations
Use in the elderly: Since the physiological functions such as
hepatic or renal function are decreased in elderly patients in general, Voniza
should be carefully administered.
Use in children less
than 18 years of age: The safety and
efficacy of Voniza in children and adolescence have not been established.
Therefore, the administration of Voniza is not recommended in children and
adolescents below 18 years of age.
Patients with renal
impairment: No dose adjustment
of Voniza is recommended in patients with mild to moderate renal impairment
(eGFR 30 to 89 mL/min). Avoid the use of Voniza in patients with severe renal
impairment (eGFR < 30 mL/min)
Patients with hepatic
impairment: No dose adjustment
of Voniza is recommended in patients with mild hepatic impairment (Child-Pugh
A). Avoid the use of Voniza in patients with moderate to severe hepatic
impairment (Child-Pugh B or C).
Overdose Effects
There is no experience
of overdose with Voniza. Voniza is not removed from the circulation by
hemodialysis. If overdose occurs, treatment should be symptomatic and
supportive.
Therapeutic Class
Potassium competitive
acid blocker
Storage Conditions
Store below 30°C, in a
cool and dry place. Keep away from light. Keep all the medicine out of the
reach of children.
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