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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 PREGABALIN Cause Intentional dose omission? 122 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 122 reports of Intentional dose omission have been filed in association with PREGABALIN (Pregabalin). This represents 0.1% of all adverse event reports for PREGABALIN.

122
Reports of Intentional dose omission with PREGABALIN
0.1%
of all PREGABALIN reports
1
Deaths
15
Hospitalizations

How Dangerous Is Intentional dose omission From PREGABALIN?

Of the 122 reports, 1 (0.8%) resulted in death, 15 (12.3%) required hospitalization, and 1 (0.8%) were considered life-threatening.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PREGABALIN. However, 122 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which PREGABALIN Alternatives Have Lower Intentional dose omission Risk?

PREGABALIN vs PREMARIN PREGABALIN vs PREMPRO PREGABALIN vs PRETOMANID PREGABALIN vs PREVISCAN PREGABALIN vs PREZISTA

Related Pages

PREGABALIN Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission PREGABALIN Demographics