Does BEDAQUILINE Cause Intentional product use issue? 181 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 181 reports of Intentional product use issue have been filed in association with BEDAQUILINE (SIRTURO). This represents 5.0% of all adverse event reports for BEDAQUILINE.
181
Reports of Intentional product use issue with BEDAQUILINE
5.0%
of all BEDAQUILINE reports
67
Deaths
79
Hospitalizations
How Dangerous Is Intentional product use issue From BEDAQUILINE?
Of the 181 reports, 67 (37.0%) resulted in death, 79 (43.6%) required hospitalization, and 20 (11.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEDAQUILINE. However, 181 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)
Tuberculosis (173)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BEDAQUILINE Alternatives Have Lower Intentional product use issue Risk?
BEDAQUILINE vs BELANTAMAB MAFODOTIN
BEDAQUILINE vs BELANTAMAB MAFODOTIN-BLMF
BEDAQUILINE vs BELATACEPT
BEDAQUILINE vs BELIMUMAB
BEDAQUILINE vs BELINOSTAT