Does EMTRICITABINE Cause Wrong technique in product usage process? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong technique in product usage process have been filed in association with EMTRICITABINE (Truvada). This represents 0.2% of all adverse event reports for EMTRICITABINE.
6
Reports of Wrong technique in product usage process with EMTRICITABINE
0.2%
of all EMTRICITABINE reports
5
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From EMTRICITABINE?
Of the 6 reports, 5 (83.3%) resulted in death.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EMTRICITABINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does EMTRICITABINE Cause?
Foetal exposure during pregnancy (609)
Drug resistance (370)
Virologic failure (331)
Immune reconstitution inflammatory syndrome (262)
Exposure during pregnancy (212)
Drug ineffective (196)
Pathogen resistance (166)
Viral mutation identified (161)
Maternal exposure during pregnancy (160)
Death (154)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which EMTRICITABINE Alternatives Have Lower Wrong technique in product usage process Risk?
EMTRICITABINE vs EMTRICITABINE\RILPIVIRINE\TENOFOVIR ALAFENAMIDE
EMTRICITABINE vs EMTRICITABINE\RILPIVIRINE\TENOFOVIR DISOPROXIL
EMTRICITABINE vs EMTRICITABINE\TENOFOVIR
EMTRICITABINE vs EMTRICITABINE\TENOFOVIR ALAFENAMIDE
EMTRICITABINE vs EMTRICITABINE/TENOFOVIR DISOPROXIL