Does PIMAVANSERIN Cause Product dose omission? 511 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 511 reports of Product dose omission have been filed in association with PIMAVANSERIN (pimavanserin). This represents 1.1% of all adverse event reports for PIMAVANSERIN.
511
Reports of Product dose omission with PIMAVANSERIN
1.1%
of all PIMAVANSERIN reports
108
Deaths
139
Hospitalizations
How Dangerous Is Product dose omission From PIMAVANSERIN?
Of the 511 reports, 108 (21.1%) resulted in death, 139 (27.2%) required hospitalization, and 2 (0.4%) 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 PIMAVANSERIN. However, 511 reports have been filed with the FAERS database.
What Other Side Effects Does PIMAVANSERIN Cause?
Hallucination (10,839)
Death (9,352)
Drug ineffective (5,545)
Product dose omission issue (3,808)
Confusional state (3,779)
Fall (3,366)
Delusion (2,421)
Hallucination, visual (1,954)
Gait disturbance (1,923)
Parkinson's disease (1,918)
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 PIMAVANSERIN Alternatives Have Lower Product dose omission Risk?
PIMAVANSERIN vs PIMECROLIMUS
PIMAVANSERIN vs PIMOZIDE
PIMAVANSERIN vs PINAVERIUM
PIMAVANSERIN vs PINDOLOL
PIMAVANSERIN vs PIOGLITAZONE