Does BEDAQUILINE Cause Incorrect product administration duration? 54 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of Incorrect product administration duration have been filed in association with BEDAQUILINE (SIRTURO). This represents 1.5% of all adverse event reports for BEDAQUILINE.
54
Reports of Incorrect product administration duration with BEDAQUILINE
1.5%
of all BEDAQUILINE reports
25
Deaths
22
Hospitalizations
How Dangerous Is Incorrect product administration duration From BEDAQUILINE?
Of the 54 reports, 25 (46.3%) resulted in death, 22 (40.7%) required hospitalization, and 1 (1.9%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEDAQUILINE. However, 54 reports have been filed with the FAERS database.
What Other Side Effects Does BEDAQUILINE Cause?
Electrocardiogram qt prolonged (593)
Off label use (419)
Anaemia (359)
Vomiting (294)
Neuropathy peripheral (259)
Hepatotoxicity (254)
Death (241)
Nausea (236)
Dyspnoea (200)
Intentional product use issue (181)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which BEDAQUILINE Alternatives Have Lower Incorrect product administration duration Risk?
BEDAQUILINE vs BELANTAMAB MAFODOTIN
BEDAQUILINE vs BELANTAMAB MAFODOTIN-BLMF
BEDAQUILINE vs BELATACEPT
BEDAQUILINE vs BELIMUMAB
BEDAQUILINE vs BELINOSTAT