Does METHYLPHENIDATE Cause Suspected product quality issue? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Suspected product quality issue have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.1% of all adverse event reports for METHYLPHENIDATE.
15
Reports of Suspected product quality issue with METHYLPHENIDATE
0.1%
of all METHYLPHENIDATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Suspected product quality issue From METHYLPHENIDATE?
Of the 15 reports.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 15 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which METHYLPHENIDATE Alternatives Have Lower Suspected product quality issue Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE