AMISULPRIDE and AKATHISIA

Overview

AKATHISIA is the #9 most commonly reported adverse reaction for AMISULPRIDE, manufactured by Acacia Pharma Ltd. There are 299 FDA adverse event reports linking AMISULPRIDE to AKATHISIA. This represents approximately 1.8% of all 16,736 adverse event reports for this drug.

Patients taking AMISULPRIDE who experience akathisia 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

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

Other Side Effects of AMISULPRIDE

In addition to akathisia, the following adverse reactions have been reported for AMISULPRIDE:

• DRUG INEFFECTIVE — 825 reports
• DRUG INTERACTION — 442 reports
• WEIGHT INCREASED — 426 reports
• TOXICITY TO VARIOUS AGENTS — 382 reports
• NEUTROPENIA — 379 reports
• SCHIZOPHRENIA — 320 reports
• LEUKOPENIA — 311 reports
• OFF LABEL USE — 305 reports
• EXTRAPYRAMIDAL DISORDER — 278 reports
• SUICIDE ATTEMPT — 277 reports

Other Drugs Associated with AKATHISIA

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

Does AMISULPRIDE cause AKATHISIA?

AKATHISIA has been reported as an adverse event in 299 FDA reports for AMISULPRIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is AKATHISIA with AMISULPRIDE?

AKATHISIA accounts for approximately 1.8% of all adverse event reports for AMISULPRIDE, making it a notable side effect.

What should I do if I experience AKATHISIA while taking AMISULPRIDE?

If you experience akathisia while taking AMISULPRIDE, 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.

Related Pages