Does EFINACONAZOLE Cause Product dose omission issue? 107 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 107 reports of Product dose omission issue have been filed in association with EFINACONAZOLE (JUBLIA). This represents 8.3% of all adverse event reports for EFINACONAZOLE.
107
Reports of Product dose omission issue with EFINACONAZOLE
8.3%
of all EFINACONAZOLE reports
30
Deaths
101
Hospitalizations
How Dangerous Is Product dose omission issue From EFINACONAZOLE?
Of the 107 reports, 30 (28.0%) resulted in death, 101 (94.4%) required hospitalization, and 29 (27.1%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EFINACONAZOLE. However, 107 reports have been filed with the FAERS database.
What Other Side Effects Does EFINACONAZOLE Cause?
Drug ineffective (344)
Pain (149)
Headache (138)
Oedema peripheral (136)
Drug hypersensitivity (135)
Fatigue (135)
Asthenia (133)
Musculoskeletal stiffness (133)
Anaemia (132)
Pyrexia (131)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which EFINACONAZOLE Alternatives Have Lower Product dose omission issue Risk?
EFINACONAZOLE vs EFLORNITHINE
EFINACONAZOLE vs EFMOROCTOCOG ALFA
EFINACONAZOLE vs EFTRENONACOG ALFA
EFINACONAZOLE vs EGG PHOSPHOLIPIDS\GLYCERIN\MEDIUM-CHAIN TRIGLYCERIDES\SOYBEAN OIL
EFINACONAZOLE vs EGG PHOSPHOLIPIDS\GLYCERIN\SOYBEAN OIL