Does DEXMETHYLPHENIDATE Cause Product dose omission? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission have been filed in association with DEXMETHYLPHENIDATE (DEXMETHYLPHENIDATE HYDROCHLORIDE). This represents 0.7% of all adverse event reports for DEXMETHYLPHENIDATE.
14
Reports of Product dose omission with DEXMETHYLPHENIDATE
0.7%
of all DEXMETHYLPHENIDATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From DEXMETHYLPHENIDATE?
Of the 14 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXMETHYLPHENIDATE. However, 14 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which DEXMETHYLPHENIDATE Alternatives Have Lower Product dose omission Risk?
DEXMETHYLPHENIDATE vs DEXMETHYLPHENIDATE\SERDEXMETHYLPHENIDATE
DEXMETHYLPHENIDATE vs DEXPANTHENOL
DEXMETHYLPHENIDATE vs DEXRAZOXANE
DEXMETHYLPHENIDATE vs DEXTRAN 70\HYPROMELLOSE 2910
DEXMETHYLPHENIDATE vs DEXTROAMPHETAMINE