Drugplain

ALVIMOPAN 12 mg/1

ALVIMOPAN · CAPSULE · Par Health USA, LLC

No Recall History
Plain English

ALVIMOPAN is a capsule containing alvimopan at 12 mg/1, taken oral. Manufactured by Par Health USA, LLC.

Key Facts

Brand Name
ALVIMOPAN
Generic Name
ALVIMOPAN
NDC Code (Product)
0254-3012
Manufacturer
Par Health USA, LLC
Strength
12 mg/1
Dosage Form
CAPSULE
Route
ORAL
Marketing Status
Application #
ANDA216843
Marketing Start
05/03/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

hospitalisation19 reports
acute kidney injury5 reports
acute myocardial infarction4 reports
ileus3 reports
pruritus3 reports
urinary retention3 reports
adenocarcinoma of colon2 reports
cardio-respiratory arrest2 reports
chronic kidney disease2 reports
dizziness2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE Alvimopan capsules are indicated to accelerate the time to upper and lower gastrointestinal recovery following surgeries that include partial bowel resection with primary anastomosis. Alvimopan capsules are an opioid antagonist indicated to accelerate the time to upper and lower gastrointestinal recovery following surgeries that include partial bowel resection with primary anastomosis. ( 1 )

Dosage & Administration

2 DOSAGE AND ADMINISTRATION For hospital use only. The recommended adult dosage of alvimopan capsules is 12 mg administered 30 minutes to 5 hours prior to surgery followed by 12 mg twice daily beginning the day after surgery until discharge for a maximum of 7 days. Patients should not receive more than 15 doses of alvimopan capsules. Alvimopan capsules can be taken with or without food [see Clinical Pharmacology ( 12.3 )] . For hospital use only. ( 2 ) The recommended dosage is 12 mg administered 30 minutes to 5 hours prior to surgery followed by 12 mg twice daily beginning the day after surgery until discharge for a maximum of 7 days. Patients should not receive more than 15 doses of alvimopan capsules. ( 2 )

Contraindications

4 CONTRAINDICATIONS Alvimopan capsules are contraindicated in patients who have taken therapeutic doses of opioids for more than 7 consecutive days immediately prior to taking alvimopan capsules [see Warnings and Precautions ( 5.3 )] . Patients who have taken therapeutic doses of opioids for more than 7 consecutive days prior to taking alvimopan capsules. ( 4 )

Drug Interactions

7 DRUG INTERACTIONS 7.1 Effects of Alvimopan on Intravenous Morphine Coadministration of alvimopan does not appear to alter the pharmacokinetics of morphine and its metabolite, morphine-6-glucuronide, to a clinically significant degree when morphine is administered intravenously. Dosage adjustment for intravenously administered morphine is not necessary when it is coadministered with alvimopan. 7.2 Effects of Concomitant Acid Blockers or Antibiotics A population pharmacokinetic analysis suggests that the pharmacokinetics of alvimopan were not affected by concomitant administration of acid blockers (proton pump inhibitors (PPIs), histamine-2 (H 2 ) receptor antagonists) or antibiotics. No dosage adjustments are necessary in patients taking acid blockers or antibiotics with alvimopan.

Adverse Reactions

6 ADVERSE REACTIONS The following clinically significant adverse reactions are described elsewhere in the labeling: Potential Risk of Myocardial Infarction with Long-Term Use [see Warnings and Precautions ( 5.1 )] Gastrointestinal-Related Adverse Reactions in Opioid-Tolerant Patients [see Warnings and Precautions ( 5.3 )] Risk of Serious Adverse Reactions in Patients with Severe Hepatic Impairment [see Warnings and Precautions ( 5.4 )] Risk of Serious Adverse Reactions in Patients with Complete Gastrointestinal Obstruction [see Warnings and Precautions ( 5.6 )] Risk of Serious Adverse Reactions in Pancreatic and Gastric Anastomoses [see Warnings and Precautions ( 5.7 )] Most common adverse reaction (≥1.5%): dyspepsia. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Hikma Pharmaceuticals USA Inc. at 1-800-962-8364 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be compared directly with rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. The adverse

Frequently Asked Questions

What is ALVIMOPAN used for?

ALVIMOPAN contains ALVIMOPAN. It is a capsule taken oral. Consult your doctor for specific uses.

Is ALVIMOPAN a controlled substance?

ALVIMOPAN is not classified as a controlled substance by the DEA.

What is the generic name for ALVIMOPAN?

The generic name for ALVIMOPAN is ALVIMOPAN. There are 3 other brand versions of ALVIMOPAN.

What is the NDC code for ALVIMOPAN 12 mg/1?

The NDC (National Drug Code) for ALVIMOPAN 12 mg/1 is 0254-3012, listed by Par Health USA, LLC.

Product NDC

0254-3012

Package NDC

0254-3012-55

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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