BARHEMSYS ® is indicated in adults for: prevention of postoperative nausea and vomiting (PONV), either alone or in combination with an antiemetic of a different class. treatment of PONV in patients who have received antiemetic prophylaxis with an agent of a different class or have not received prophylaxis.
From the U.S. FDA-approved label for Amisulpride. Full label: DailyMed.
BARHEMSYS ® is indicated in adults for: prevention of postoperative nausea and vomiting (PONV), either alone or in combination with an antiemetic of a different class. treatment of PONV in patients who have received antiemetic prophylaxis with an agent of a different class or have not received prophylaxis.
From the U.S. FDA-approved label for Amisulpride. Full label: DailyMed.
The recommended dosage of BARHEMSYS: Prevention of PONV, either alone or in combination with another antiemetic: 5 mg as a single intravenous dose infused over 1 to 2 minutes at the time of induction of anesthesia. Treatment of PONV: 10 mg as a single intravenous dose infused over 1 to 2 minutes in the event of nausea and/or vomiting after a surgical procedure. See full prescribing information for preparation and administration instructions.
Directions from the U.S. FDA-approved label for Amisulpride — your doctor or pharmacist may advise differently.
BARHEMSYS is contraindicated in patients with known hypersensitivity to amisulpride. Known hypersensitivity to amisulpride.
Excerpt from the U.S. FDA-approved label for Amisulpride. Talk to a pharmacist or doctor before use.
QT Prolongation: Occurs in a dose- and concentration-dependent manner. Avoid use in patients with congenital long QT syndrome and in patients taking droperidol. ECG monitoring is recommended in patients with pre-existing arrhythmias/cardiac conduction disorders; electrolyte abnormalities (e.g., hypokalemia or hypomagnesemia); congestive heart failure; and in patients taking other medicinal products (e.g., ondansetron) or with other medical conditions known to prolong the QT interval. 5.1 QT Prolongation BARHEMSYS causes dose- and concentration-dependent prolongation of the QT interval.
Warnings and precautions excerpt from the U.S. FDA-approved label for Amisulpride — not a complete list. Talk to a pharmacist or doctor before use.
Most common adverse reactions (≥ 2%) are: Prevention of PONV: increased blood prolactin concentrations, chills, hypokalemia, procedural hypotension, and abdominal distension. Treatment of PONV: infusion site pain. To report SUSPECTED ADVERSE REACTIONS, contact Acacia Pharma at 1-877-357-9237 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Excerpt from the U.S. FDA-approved label for Amisulpride — not a complete list. Talk to a pharmacist or doctor about side effects.
17 brands · 5 makers in the NepalDoc catalog — see the full Amisulpride guide →
Store vials at 20°C to 25°C (68°F to 77°F). Protect from light. Administer BARHEMSYS within 12 hours after the vial is removed from the protective carton.
Storage information from the U.S. FDA-approved label for Amisulpride.
What is Soltus?
Soltus 100mg Tablet is a Amisulpride medicine made by Intas Pharmaceuticals Ltd. It comes as 100mg Tablet.
What is the generic name of Soltus?
The generic name of Soltus is Amisulpride.
Which brands of Amisulpride are available in Nepal?
17 brands of Amisulpride are listed in the NepalDoc catalog, from 5 makers — including Amride 100mg Tablet, Amride 50mg Tablet, Maxpride 100mg Tablet, Maxpride 200mg Tablet, Maxpride 50mg Tablet, Solpride 100mg Tablet.
What are the side effects of Amisulpride?
Most common adverse reactions (≥ 2%) are: Prevention of PONV: increased blood prolactin concentrations, chills, hypokalemia, procedural hypotension, and abdominal distension. Treatment of PONV: infusion site pain.
This page is information only and is not medical advice. Medicine details come from the sources listed above and may change — always confirm the medicine, strength and dose with a pharmacist or doctor before use. A catalog listing does not guarantee that a medicine is in stock at any pharmacy.
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