Does PREGABALIN Cause Product dose omission issue? 471 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 471 reports of Product dose omission issue have been filed in association with PREGABALIN (Pregabalin). This represents 0.5% of all adverse event reports for PREGABALIN.
471
Reports of Product dose omission issue with PREGABALIN
0.5%
of all PREGABALIN reports
11
Deaths
172
Hospitalizations
How Dangerous Is Product dose omission issue From PREGABALIN?
Of the 471 reports, 11 (2.3%) resulted in death, 172 (36.5%) required hospitalization, and 16 (3.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PREGABALIN. However, 471 reports have been filed with the FAERS database.
What Other Side Effects Does PREGABALIN Cause?
Drug ineffective (13,664)
Pain (12,996)
Malaise (6,320)
Dizziness (5,878)
Off label use (5,713)
Somnolence (5,528)
Pain in extremity (5,023)
Fatigue (4,909)
Weight increased (4,903)
Condition aggravated (4,901)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which PREGABALIN Alternatives Have Lower Product dose omission issue Risk?
PREGABALIN vs PREMARIN
PREGABALIN vs PREMPRO
PREGABALIN vs PRETOMANID
PREGABALIN vs PREVISCAN
PREGABALIN vs PREZISTA