Does PRETOMANID Cause Off label use? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Off label use have been filed in association with PRETOMANID (Pretomanid). This represents 4.6% of all adverse event reports for PRETOMANID.
23
Reports of Off label use with PRETOMANID
4.6%
of all PRETOMANID reports
8
Deaths
6
Hospitalizations
How Dangerous Is Off label use From PRETOMANID?
Of the 23 reports, 8 (34.8%) resulted in death, 6 (26.1%) required hospitalization, and 2 (8.7%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRETOMANID. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does PRETOMANID Cause?
Death (91)
Anaemia (43)
Nausea (32)
Electrocardiogram qt prolonged (30)
Neuropathy peripheral (26)
Acute kidney injury (25)
Hepatotoxicity (22)
Alanine aminotransferase increased (21)
Aspartate aminotransferase increased (19)
Decreased appetite (14)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which PRETOMANID Alternatives Have Lower Off label use Risk?
PRETOMANID vs PREVISCAN
PRETOMANID vs PREZISTA
PRETOMANID vs PRILOCAINE
PRETOMANID vs PRILOSEC
PRETOMANID vs PRILOSEC OTC