Does CABOTEGRAVIR Cause Condition aggravated? 145 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 145 reports of Condition aggravated have been filed in association with CABOTEGRAVIR (Apretude). This represents 1.8% of all adverse event reports for CABOTEGRAVIR.
145
Reports of Condition aggravated with CABOTEGRAVIR
1.8%
of all CABOTEGRAVIR reports
2
Deaths
12
Hospitalizations
How Dangerous Is Condition aggravated From CABOTEGRAVIR?
Of the 145 reports, 2 (1.4%) resulted in death, 12 (8.3%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABOTEGRAVIR. However, 145 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CABOTEGRAVIR Alternatives Have Lower Condition aggravated Risk?
CABOTEGRAVIR vs CABOTEGRAVIR\RILPIVIRINE
CABOTEGRAVIR vs CABOZANTINIB
CABOTEGRAVIR vs CABOZANTINIB S-MALATE
CABOTEGRAVIR vs CAFFEINE
CABOTEGRAVIR vs CALASPARGASE PEGOL