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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AMANTADINE Cause Product dose omission? 73 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Product dose omission have been filed in association with AMANTADINE (Amantadine). This represents 1.4% of all adverse event reports for AMANTADINE.

73
Reports of Product dose omission with AMANTADINE
1.4%
of all AMANTADINE reports
13
Deaths
40
Hospitalizations

How Dangerous Is Product dose omission From AMANTADINE?

Of the 73 reports, 13 (17.8%) resulted in death, 40 (54.8%) required hospitalization, and 1 (1.4%) were considered life-threatening.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMANTADINE. However, 73 reports have been filed with the FAERS database.

What Other Side Effects Does AMANTADINE Cause?

Fall (594) Hallucination (584) Drug ineffective (519) Dyskinesia (470) Dizziness (379) Tremor (347) Off label use (346) Gait disturbance (317) Fatigue (292) Hallucination, visual (277)

What Other Drugs Cause Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which AMANTADINE Alternatives Have Lower Product dose omission Risk?

AMANTADINE vs AMBIEN AMANTADINE vs AMBISOME AMANTADINE vs AMBRISENTAN AMANTADINE vs AMBROSIA ARTEMISIIFOLIA POLLEN AMANTADINE vs AMBROXOL

Related Pages

AMANTADINE Full Profile All Product dose omission Reports All Drugs Causing Product dose omission AMANTADINE Demographics