Does METHYLPHENIDATE Cause Expired product administered? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Expired product administered have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.2% of all adverse event reports for METHYLPHENIDATE.
59
Reports of Expired product administered with METHYLPHENIDATE
0.2%
of all METHYLPHENIDATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Expired product administered From METHYLPHENIDATE?
Of the 59 reports.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 59 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which METHYLPHENIDATE Alternatives Have Lower Expired product administered Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE