Does DEXMETHYLPHENIDATE Cause Wrong product administered? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Wrong product administered have been filed in association with DEXMETHYLPHENIDATE (DEXMETHYLPHENIDATE HYDROCHLORIDE). This represents 0.4% of all adverse event reports for DEXMETHYLPHENIDATE.
8
Reports of Wrong product administered with DEXMETHYLPHENIDATE
0.4%
of all DEXMETHYLPHENIDATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong product administered From DEXMETHYLPHENIDATE?
Of the 8 reports.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXMETHYLPHENIDATE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does DEXMETHYLPHENIDATE Cause?
Drug ineffective (663)
Product substitution issue (148)
Disturbance in attention (129)
Decreased appetite (121)
Anxiety (116)
Abnormal behaviour (113)
Headache (112)
Feeling abnormal (106)
Nausea (85)
Treatment failure (80)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which DEXMETHYLPHENIDATE Alternatives Have Lower Wrong product administered Risk?
DEXMETHYLPHENIDATE vs DEXMETHYLPHENIDATE\SERDEXMETHYLPHENIDATE
DEXMETHYLPHENIDATE vs DEXPANTHENOL
DEXMETHYLPHENIDATE vs DEXRAZOXANE
DEXMETHYLPHENIDATE vs DEXTRAN 70\HYPROMELLOSE 2910
DEXMETHYLPHENIDATE vs DEXTROAMPHETAMINE