Does PEGVISOMANT Cause Intentional product misuse? 79 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Intentional product misuse have been filed in association with PEGVISOMANT (SOMAVERT). This represents 2.6% of all adverse event reports for PEGVISOMANT.
79
Reports of Intentional product misuse with PEGVISOMANT
2.6%
of all PEGVISOMANT reports
1
Deaths
14
Hospitalizations
How Dangerous Is Intentional product misuse From PEGVISOMANT?
Of the 79 reports, 1 (1.3%) resulted in death, 14 (17.7%) required hospitalization, and 1 (1.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGVISOMANT. However, 79 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which PEGVISOMANT Alternatives Have Lower Intentional product misuse Risk?
PEGVISOMANT vs PEGZEREPOETIN ALFA
PEGVISOMANT vs PEMBROLIZUMAB
PEGVISOMANT vs PEMETREXED
PEGVISOMANT vs PEMIGATINIB
PEGVISOMANT vs PENICILLAMINE