AMMONIUM LACTATE and FALL

Overview

FALL is the #10 most commonly reported adverse reaction for AMMONIUM LACTATE, manufactured by Padagis Israel Pharmaceuticals Ltd. There are 95 FDA adverse event reports linking AMMONIUM LACTATE to FALL. This represents approximately 2.1% of all 4,560 adverse event reports for this drug.

Patients taking AMMONIUM LACTATE who experience fall 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

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

Other Side Effects of AMMONIUM LACTATE

In addition to fall, the following adverse reactions have been reported for AMMONIUM LACTATE:

• PAIN — 138 reports
• FATIGUE — 137 reports
• CHRONIC KIDNEY DISEASE — 127 reports
• DIARRHOEA — 127 reports
• DRUG INEFFECTIVE — 120 reports
• NAUSEA — 114 reports
• RASH — 102 reports
• DYSPNOEA — 101 reports
• RENAL FAILURE — 99 reports
• HEADACHE — 93 reports

Other Drugs Associated with FALL

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

Does AMMONIUM LACTATE cause FALL?

FALL has been reported as an adverse event in 95 FDA reports for AMMONIUM LACTATE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is FALL with AMMONIUM LACTATE?

FALL accounts for approximately 2.1% of all adverse event reports for AMMONIUM LACTATE, making it a notable side effect.

What should I do if I experience FALL while taking AMMONIUM LACTATE?

If you experience fall while taking AMMONIUM 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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