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milrinone

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Brand names: Primacor

Phosphodiesterase-3 Inhibitor Rx

Milrinone is a medicine used in the hospital for a short time to help people with severe heart failure. It helps your heart pump better.

What it does

Milrinone is used for the short-term treatment of acute decompensated heart failure.

Common side effects

Irregular heartbeats

Key warnings

Be careful.

How It Works

Milrinone belongs to a class of drugs called phosphodiesterase-3 inhibitors. It makes more of a substance called cAMP available to your heart and blood vessels. This helps your heart muscle squeeze harder and widens your blood vessels, so blood flows more easily.

How to Take It

Milrinone is given into your vein through an IV. First, you'll get a loading dose over 10 minutes. Then, you'll get a continuous infusion. The amount you get depends on your weight and how well the medicine is working. Your doctor will adjust the dose as needed.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or breastfeeding. It is not known if milrinone will harm your unborn baby. It is also not known if milrinone passes into breast milk.

Missed Dose

Since this medicine is given in a hospital, you don't have to worry about missing a dose.

Storage

Milrinone should be stored at room temperature, away from freezing.

Serious Warnings

Be careful. Milrinone can cause life-threatening irregular heartbeats. Your doctor will watch your heart closely while you are taking this medicine.

Common Questions

What should I tell my doctor before taking milrinone?
Tell your doctor if you are allergic to milrinone or any of the other ingredients in the injection. Also, tell your doctor about all of your medical conditions, including any heart problems.
How will I be monitored while taking milrinone?
Your doctor will closely monitor your heart with an EKG machine. They will also check your blood pressure and other vital signs.
What are the possible side effects of milrinone?
Milrinone can cause irregular heartbeats, low blood pressure, and headaches. Tell your doctor if you experience any new or worsening symptoms.
Can milrinone interact with other medications?
Yes, milrinone can interact with other medications, including digoxin and diuretics. Tell your doctor about all the medications you are taking.
How long will I need to take milrinone?
Milrinone is only for short-term use. Your doctor will decide how long you need to take it.
What if I have kidney problems?
Your doctor may need to adjust your dose of milrinone if you have kidney problems.
Can milrinone cause chest pain?
Yes, some people taking milrinone have reported chest pain.
What if I have low potassium?
Low potassium can increase the risk of irregular heartbeats with milrinone. Your doctor will check your potassium levels.
Can milrinone cause liver problems?
In rare cases, milrinone has been linked to abnormal liver function tests.
What if I have a skin reaction?
Skin reactions like rash have been reported with milrinone. Tell your doctor if you develop a rash.
What are the common side effects of milrinone?
The most commonly reported side effects of milrinone include Irregular heartbeats. Always consult your healthcare provider about potential side effects.
What drug class is milrinone?
milrinone belongs to the Phosphodiesterase-3 Inhibitor drug class. It requires a prescription (Rx). Milrinone is used for the short-term treatment of acute decompensated heart failure.
Is milrinone safe during pregnancy?
Tell your doctor if you are pregnant or breastfeeding. It is not known if milrinone will harm your unborn baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

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What the FDA Data Shows for milrinone

The FDA label for milrinone (sold under brand names such as Primacor) classifies it as a prescription-only medication in the Phosphodiesterase-3 Inhibitor class. Milrinone is used for the short-term treatment of acute decompensated heart failure. Official labeling lists 1 commonly reported side effect, including Irregular heartbeats.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.

Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: January 15, 2025

All federal data sources used on this page