Does CABOTEGRAVIR Cause Wrong technique in device usage process? 124 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 124 reports of Wrong technique in device usage process have been filed in association with CABOTEGRAVIR (Apretude). This represents 1.5% of all adverse event reports for CABOTEGRAVIR.
124
Reports of Wrong technique in device usage process with CABOTEGRAVIR
1.5%
of all CABOTEGRAVIR reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in device usage process From CABOTEGRAVIR?
Of the 124 reports, 1 (0.8%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABOTEGRAVIR. However, 124 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 Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which CABOTEGRAVIR Alternatives Have Lower Wrong technique in device usage process Risk?
CABOTEGRAVIR vs CABOTEGRAVIR\RILPIVIRINE
CABOTEGRAVIR vs CABOZANTINIB
CABOTEGRAVIR vs CABOZANTINIB S-MALATE
CABOTEGRAVIR vs CAFFEINE
CABOTEGRAVIR vs CALASPARGASE PEGOL