Does NITISINONE Cause Product dose omission issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product dose omission issue have been filed in association with NITISINONE (Nitisinone). This represents 2.4% of all adverse event reports for NITISINONE.
18
Reports of Product dose omission issue with NITISINONE
2.4%
of all NITISINONE reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission issue From NITISINONE?
Of the 18 reports, 2 (11.1%) resulted in death, 7 (38.9%) 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 NITISINONE. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does NITISINONE Cause?
Amino acid level increased (118)
Liver transplant (62)
Hepatocellular carcinoma (58)
Cataract (47)
Off label use (41)
Alpha 1 foetoprotein increased (39)
Lenticular opacities (34)
Vomiting (32)
Succinylacetone increased (31)
Treatment noncompliance (30)
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 NITISINONE Alternatives Have Lower Product dose omission issue Risk?
NITISINONE vs NITRAZEPAM
NITISINONE vs NITRENDIPINE
NITISINONE vs NITRIC
NITISINONE vs NITROFURANTOIN
NITISINONE vs NITROFURANTOIN\NITROFURANTOIN