Does PYRILAMINE Cause Product dose omission issue? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Product dose omission issue have been filed in association with PYRILAMINE (Childrens PediaClear 8). This represents 71.9% of all adverse event reports for PYRILAMINE.
46
Reports of Product dose omission issue with PYRILAMINE
71.9%
of all PYRILAMINE reports
0
Deaths
46
Hospitalizations
How Dangerous Is Product dose omission issue From PYRILAMINE?
Of the 46 reports, 46 (100.0%) required hospitalization, and 1 (2.2%) 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 PYRILAMINE. However, 46 reports have been filed with the FAERS database.
What Other Side Effects Does PYRILAMINE Cause?
Drug ineffective (47)
Drug hypersensitivity (46)
General physical health deterioration (46)
Constipation (45)
Anaemia (44)
Aspiration (44)
Asthma (44)
Blood calcium increased (44)
Blood creatinine increased (44)
Bronchopulmonary aspergillosis allergic (44)
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)