Does METHYLPHENIDATE Cause Device breakage? 222 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 222 reports of Device breakage have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 0.7% of all adverse event reports for METHYLPHENIDATE.
222
Reports of Device breakage with METHYLPHENIDATE
0.7%
of all METHYLPHENIDATE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device breakage From METHYLPHENIDATE?
Of the 222 reports, 2 (0.9%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 222 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which METHYLPHENIDATE Alternatives Have Lower Device breakage Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE