Does HYDROXYUREA Cause Product dose omission issue? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Product dose omission issue have been filed in association with HYDROXYUREA (Hydroxyurea). This represents 0.9% of all adverse event reports for HYDROXYUREA.
55
Reports of Product dose omission issue with HYDROXYUREA
0.9%
of all HYDROXYUREA reports
0
Deaths
18
Hospitalizations
How Dangerous Is Product dose omission issue From HYDROXYUREA?
Of the 55 reports, 18 (32.7%) required hospitalization, and 1 (1.8%) 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 HYDROXYUREA. However, 55 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXYUREA Cause?
Off label use (519)
Anaemia (358)
Drug ineffective (356)
Fatigue (291)
Thrombocytopenia (253)
Nausea (247)
Pyrexia (243)
Diarrhoea (222)
Febrile neutropenia (202)
Intentional product use issue (201)
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 HYDROXYUREA Alternatives Have Lower Product dose omission issue Risk?
HYDROXYUREA vs HYDROXYZINE
HYDROXYUREA vs HYDROXYZINE\HYDROXYZINE
HYDROXYUREA vs HYOSCYAMINE
HYDROXYUREA vs HYPROMELLOSE 2910
HYDROXYUREA vs IBALIZUMAB-UIYK