Does DELAMANID Cause Intentional product use issue? 89 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 89 reports of Intentional product use issue have been filed in association with DELAMANID. This represents 5.4% of all adverse event reports for DELAMANID.
89
Reports of Intentional product use issue with DELAMANID
5.4%
of all DELAMANID reports
43
Deaths
47
Hospitalizations
How Dangerous Is Intentional product use issue From DELAMANID?
Of the 89 reports, 43 (48.3%) resulted in death, 47 (52.8%) required hospitalization, and 7 (7.9%) 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 DELAMANID. However, 89 reports have been filed with the FAERS database.
What Other Side Effects Does DELAMANID Cause?
Electrocardiogram qt prolonged (263)
Vomiting (237)
Anaemia (209)
Off label use (207)
Dyspnoea (160)
Neuropathy peripheral (135)
Nausea (126)
Haemoglobin decreased (104)
Tuberculosis (94)
Asthenia (81)
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 DELAMANID Alternatives Have Lower Intentional product use issue Risk?
DELAMANID vs DELANDISTROGENE MOXEPARVOVEC-ROKL
DELAMANID vs DELAVIRDINE
DELAMANID vs DELORAZEPAM
DELAMANID vs DELTA.8-TETRAHYDROCANNABINOL\HERBALS
DELAMANID vs DEMCIZUMAB