Does METHYLPHENIDATE Cause Product prescribing error? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Product prescribing error have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.2% of all adverse event reports for METHYLPHENIDATE.
53
Reports of Product prescribing error with METHYLPHENIDATE
0.2%
of all METHYLPHENIDATE reports
1
Deaths
4
Hospitalizations
How Dangerous Is Product prescribing error From METHYLPHENIDATE?
Of the 53 reports, 1 (1.9%) resulted in death, 4 (7.5%) required hospitalization, and 3 (5.7%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 53 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which METHYLPHENIDATE Alternatives Have Lower Product prescribing error Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE