Does PEGVISOMANT Cause Poor quality product administered? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Poor quality product administered have been filed in association with PEGVISOMANT (SOMAVERT). This represents 1.1% of all adverse event reports for PEGVISOMANT.
34
Reports of Poor quality product administered with PEGVISOMANT
1.1%
of all PEGVISOMANT reports
2
Deaths
6
Hospitalizations
How Dangerous Is Poor quality product administered From PEGVISOMANT?
Of the 34 reports, 2 (5.9%) resulted in death, 6 (17.6%) required hospitalization, and 1 (2.9%) were considered life-threatening.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGVISOMANT. However, 34 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which PEGVISOMANT Alternatives Have Lower Poor quality product administered Risk?
PEGVISOMANT vs PEGZEREPOETIN ALFA
PEGVISOMANT vs PEMBROLIZUMAB
PEGVISOMANT vs PEMETREXED
PEGVISOMANT vs PEMIGATINIB
PEGVISOMANT vs PENICILLAMINE