Does METHYLPHENIDATE Cause Product use issue? 498 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 498 reports of Product use issue have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 1.6% of all adverse event reports for METHYLPHENIDATE.
498
Reports of Product use issue with METHYLPHENIDATE
1.6%
of all METHYLPHENIDATE reports
9
Deaths
73
Hospitalizations
How Dangerous Is Product use issue From METHYLPHENIDATE?
Of the 498 reports, 9 (1.8%) resulted in death, 73 (14.7%) required hospitalization, and 14 (2.8%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 498 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which METHYLPHENIDATE Alternatives Have Lower Product use issue Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE