Does LEVOKETOCONAZOLE Cause Product dose omission issue? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product dose omission issue have been filed in association with LEVOKETOCONAZOLE (Recorlev). This represents 8.7% of all adverse event reports for LEVOKETOCONAZOLE.
27
Reports of Product dose omission issue with LEVOKETOCONAZOLE
8.7%
of all LEVOKETOCONAZOLE reports
0
Deaths
14
Hospitalizations
How Dangerous Is Product dose omission issue From LEVOKETOCONAZOLE?
Of the 27 reports, 14 (51.9%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOKETOCONAZOLE. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does LEVOKETOCONAZOLE Cause?
Nausea (108)
Fatigue (106)
Headache (84)
Vomiting (68)
Diarrhoea (45)
Dizziness (42)
Malaise (40)
Weight decreased (38)
Pain (37)
Arthralgia (36)
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 LEVOKETOCONAZOLE Alternatives Have Lower Product dose omission issue Risk?
LEVOKETOCONAZOLE vs LEVOLEUCOVORIN
LEVOKETOCONAZOLE vs LEVOMEPROMAZINE
LEVOKETOCONAZOLE vs LEVOMETHADONE
LEVOKETOCONAZOLE vs LEVOMILNACIPRAN
LEVOKETOCONAZOLE vs LEVONORGESTREL