Does CABOTEGRAVIR Cause Product use issue? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Product use issue have been filed in association with CABOTEGRAVIR (Apretude). This represents 1.1% of all adverse event reports for CABOTEGRAVIR.
92
Reports of Product use issue with CABOTEGRAVIR
1.1%
of all CABOTEGRAVIR reports
5
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From CABOTEGRAVIR?
Of the 92 reports, 5 (5.4%) resulted in death, 5 (5.4%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABOTEGRAVIR. However, 92 reports have been filed with the FAERS database.
What Other Side Effects Does CABOTEGRAVIR Cause?
Product dose omission issue (1,121)
Off label use (1,049)
Injection site pain (924)
Viral load increased (452)
Pain (399)
Virologic failure (275)
Pathogen resistance (270)
Pyrexia (255)
Product use in unapproved therapeutic environment (234)
Inappropriate schedule of product administration (228)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which CABOTEGRAVIR Alternatives Have Lower Product use issue Risk?
CABOTEGRAVIR vs CABOTEGRAVIR\RILPIVIRINE
CABOTEGRAVIR vs CABOZANTINIB
CABOTEGRAVIR vs CABOZANTINIB S-MALATE
CABOTEGRAVIR vs CAFFEINE
CABOTEGRAVIR vs CALASPARGASE PEGOL