Does PEGVISOMANT Cause Product dose omission? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Product dose omission have been filed in association with PEGVISOMANT (SOMAVERT). This represents 1.7% of all adverse event reports for PEGVISOMANT.
52
Reports of Product dose omission with PEGVISOMANT
1.7%
of all PEGVISOMANT reports
0
Deaths
9
Hospitalizations
How Dangerous Is Product dose omission From PEGVISOMANT?
Of the 52 reports, 9 (17.3%) required hospitalization, and 1 (1.9%) 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 PEGVISOMANT. However, 52 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?
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 PEGVISOMANT Alternatives Have Lower Product dose omission Risk?
PEGVISOMANT vs PEGZEREPOETIN ALFA
PEGVISOMANT vs PEMBROLIZUMAB
PEGVISOMANT vs PEMETREXED
PEGVISOMANT vs PEMIGATINIB
PEGVISOMANT vs PENICILLAMINE