DALFAMPRIDINE and DRUG DOSE OMISSION

2,151 reports of this reaction

1.4% of all DALFAMPRIDINE reports

#20 most reported adverse reaction

Overview

DRUG DOSE OMISSION is the #20 most commonly reported adverse reaction for DALFAMPRIDINE, manufactured by Merz Pharmaceuticals, LLC. There are 2,151 FDA adverse event reports linking DALFAMPRIDINE to DRUG DOSE OMISSION. This represents approximately 1.4% of all 157,067 adverse event reports for this drug.

Patients taking DALFAMPRIDINE who experience drug dose omission 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

DRUG DOSE OMISSION2,151 of 157,067 reports

DRUG DOSE OMISSION is a less commonly reported adverse event for DALFAMPRIDINE, but still significant enough to appear in the safety profile.

Other Side Effects of DALFAMPRIDINE

In addition to drug dose omission, the following adverse reactions have been reported for DALFAMPRIDINE:

GAIT DISTURBANCE — 10,928 reports
DRUG INEFFECTIVE — 8,253 reports
FALL — 7,293 reports
FATIGUE — 5,481 reports
BALANCE DISORDER — 4,878 reports
MULTIPLE SCLEROSIS RELAPSE — 4,699 reports
THERAPY CESSATION — 4,508 reports
DIZZINESS — 3,972 reports
URINARY TRACT INFECTION — 3,718 reports
CONDITION AGGRAVATED — 3,470 reports

Other Drugs Associated with DRUG DOSE OMISSION

The following drugs have also been linked to drug dose omission in FDA adverse event reports:

ACLIDINIUM BROMIDE BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE CARBAMIDE PEROXIDE 6.5%CINACALCET HYDROCHLORIDE ESOMEPRAZOLE MAGNESIUM EVOLOCUMAB FLUTICASONE PROPIONATE AND SALMETEROL INSULIN LISPRO IVACAFTOR LEDIPASVIR AND SOFOSBUVIR METHYLPHENIDATE MOMETASONE FUROATE MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE PALIPERIDONE PALMITATE PATIROMER PEGFILGRASTIM QUETIAPINE TERIPARATIDE TETRABENAZINE UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE

Frequently Asked Questions

Does DALFAMPRIDINE cause DRUG DOSE OMISSION?

DRUG DOSE OMISSION has been reported as an adverse event in 2,151 FDA reports for DALFAMPRIDINE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is DRUG DOSE OMISSION with DALFAMPRIDINE?

DRUG DOSE OMISSION accounts for approximately 1.4% of all adverse event reports for DALFAMPRIDINE, making it a notable side effect.

What should I do if I experience DRUG DOSE OMISSION while taking DALFAMPRIDINE?

If you experience drug dose omission while taking DALFAMPRIDINE, 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.

DALFAMPRIDINE Full Profile All Drugs Causing DRUG DOSE OMISSION Merz Pharmaceuticals, LLC Drugs

Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.