Does METHYLPHENIDATE Cause Device issue? 191 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 191 reports of Device issue have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.6% of all adverse event reports for METHYLPHENIDATE.
191
Reports of Device issue with METHYLPHENIDATE
0.6%
of all METHYLPHENIDATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device issue From METHYLPHENIDATE?
Of the 191 reports, 1 (0.5%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 191 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which METHYLPHENIDATE Alternatives Have Lower Device issue Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE