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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does METHYLPHENIDATE Cause Device defective? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device defective have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.0% of all adverse event reports for METHYLPHENIDATE.

11
Reports of Device defective with METHYLPHENIDATE
0.0%
of all METHYLPHENIDATE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device defective From METHYLPHENIDATE?

Of the 11 reports.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 11 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which METHYLPHENIDATE Alternatives Have Lower Device defective Risk?

METHYLPHENIDATE vs METHYLPREDNISOLONE METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE METHYLPHENIDATE vs METILDIGOXIN METHYLPHENIDATE vs METOCLOPRAMIDE

Related Pages

METHYLPHENIDATE Full Profile All Device defective Reports All Drugs Causing Device defective METHYLPHENIDATE Demographics