MILRINONE LACTATE and INJURY

Overview

INJURY is the #18 most commonly reported adverse reaction for MILRINONE LACTATE, manufactured by Baxter Healthcare Corporation. There are 7 FDA adverse event reports linking MILRINONE LACTATE to INJURY. This represents approximately 1.2% of all 574 adverse event reports for this drug.

Patients taking MILRINONE LACTATE who experience injury should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

INJURY is a less commonly reported adverse event for MILRINONE LACTATE, but still significant enough to appear in the safety profile.

Other Side Effects of MILRINONE LACTATE

In addition to injury, the following adverse reactions have been reported for MILRINONE LACTATE:

• DRUG INEFFECTIVE — 89 reports
• HYPOTENSION — 15 reports
• RENAL FAILURE — 13 reports
• CARDIAC FAILURE — 12 reports
• DYSPNOEA — 11 reports
• CARDIAC ARREST — 10 reports
• OFF LABEL USE — 10 reports
• VENTRICULAR TACHYCARDIA — 10 reports
• HAEMORRHAGE — 9 reports
• MULTI ORGAN FAILURE — 9 reports

Other Drugs Associated with INJURY

The following drugs have also been linked to injury in FDA adverse event reports:

Does MILRINONE LACTATE cause INJURY?

INJURY has been reported as an adverse event in 7 FDA reports for MILRINONE LACTATE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is INJURY with MILRINONE LACTATE?

INJURY accounts for approximately 1.2% of all adverse event reports for MILRINONE LACTATE, making it a notable side effect.

What should I do if I experience INJURY while taking MILRINONE LACTATE?

If you experience injury while taking MILRINONE LACTATE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.

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