Does METHYLPHENIDATE Cause Product dose omission issue? 600 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 600 reports of Product dose omission issue have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 1.9% of all adverse event reports for METHYLPHENIDATE.
600
Reports of Product dose omission issue with METHYLPHENIDATE
1.9%
of all METHYLPHENIDATE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product dose omission issue From METHYLPHENIDATE?
Of the 600 reports, 13 (2.2%) required hospitalization, and 1 (0.2%) 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 METHYLPHENIDATE. However, 600 reports have been filed with the FAERS database.
What Other Side Effects Does METHYLPHENIDATE Cause?
Drug ineffective (4,924)
Off label use (4,842)
No adverse event (4,197)
Product quality issue (1,728)
Disturbance in attention (1,414)
Product substitution issue (1,408)
Anxiety (1,356)
Drug dose omission (1,330)
Headache (1,255)
Wrong technique in product usage process (1,250)
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 METHYLPHENIDATE Alternatives Have Lower Product dose omission issue Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE