Does METHYLPHENIDATE Cause Product quality issue? 1,728 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,728 reports of Product quality issue have been filed in association with METHYLPHENIDATE (Methylphenidate Hydrochloride). This represents 5.6% of all adverse event reports for METHYLPHENIDATE.
1,728
Reports of Product quality issue with METHYLPHENIDATE
5.6%
of all METHYLPHENIDATE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Product quality issue From METHYLPHENIDATE?
Of the 1,728 reports, 11 (0.6%) required hospitalization, and 4 (0.2%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPHENIDATE. However, 1,728 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)
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)
Decreased appetite (1,069)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which METHYLPHENIDATE Alternatives Have Lower Product quality issue Risk?
METHYLPHENIDATE vs METHYLPREDNISOLONE
METHYLPHENIDATE vs METHYLPREDNISOLONE ACEPONATE
METHYLPHENIDATE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPHENIDATE vs METILDIGOXIN
METHYLPHENIDATE vs METOCLOPRAMIDE