PROPRANOLOL HYDROCHLORIDE and FATIGUE

Overview

FATIGUE is the #5 most commonly reported adverse reaction for PROPRANOLOL HYDROCHLORIDE, manufactured by Fresenius Kabi USA, LLC. There are 3,750 FDA adverse event reports linking PROPRANOLOL HYDROCHLORIDE to FATIGUE. This represents approximately 2.7% of all 140,640 adverse event reports for this drug.

PROPRANOLOL HYDROCHLORIDE has an overall safety score of 85 out of 100. Patients taking PROPRANOLOL HYDROCHLORIDE who experience fatigue 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

FATIGUE is a less commonly reported adverse event for PROPRANOLOL HYDROCHLORIDE, but still significant enough to appear in the safety profile.

Other Side Effects of PROPRANOLOL HYDROCHLORIDE

In addition to fatigue, the following adverse reactions have been reported for PROPRANOLOL HYDROCHLORIDE:

• OFF LABEL USE — 7,261 reports
• DRUG INEFFECTIVE — 5,332 reports
• NAUSEA — 4,279 reports
• HEADACHE — 3,782 reports
• DIARRHOEA — 3,120 reports
• DIZZINESS — 3,103 reports
• PRODUCT USE IN UNAPPROVED INDICATION — 2,837 reports
• VOMITING — 2,650 reports
• DYSPNOEA — 2,561 reports
• PRODUCT USE ISSUE — 2,488 reports

Other Drugs Associated with FATIGUE

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

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