Does PEGVISOMANT Cause Product dose omission in error? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Product dose omission in error have been filed in association with PEGVISOMANT (SOMAVERT). This represents 1.5% of all adverse event reports for PEGVISOMANT.
46
Reports of Product dose omission in error with PEGVISOMANT
1.5%
of all PEGVISOMANT reports
1
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From PEGVISOMANT?
Of the 46 reports, 1 (2.2%) resulted in death, 4 (8.7%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGVISOMANT. However, 46 reports have been filed with the FAERS database.
What Other Side Effects Does PEGVISOMANT Cause?
Off label use (460)
Drug ineffective (328)
Insulin-like growth factor increased (320)
Product dose omission issue (255)
Headache (244)
Fatigue (224)
Arthralgia (184)
Death (162)
Injection site pain (161)
Product use issue (158)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which PEGVISOMANT Alternatives Have Lower Product dose omission in error Risk?
PEGVISOMANT vs PEGZEREPOETIN ALFA
PEGVISOMANT vs PEMBROLIZUMAB
PEGVISOMANT vs PEMETREXED
PEGVISOMANT vs PEMIGATINIB
PEGVISOMANT vs PENICILLAMINE