Does DEXMETHYLPHENIDATE Cause Product packaging quantity issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product packaging quantity issue have been filed in association with DEXMETHYLPHENIDATE (DEXMETHYLPHENIDATE HYDROCHLORIDE). This represents 0.5% of all adverse event reports for DEXMETHYLPHENIDATE.
10
Reports of Product packaging quantity issue with DEXMETHYLPHENIDATE
0.5%
of all DEXMETHYLPHENIDATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product packaging quantity issue From DEXMETHYLPHENIDATE?
Of the 10 reports.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXMETHYLPHENIDATE. However, 10 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 packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which DEXMETHYLPHENIDATE Alternatives Have Lower Product packaging quantity issue Risk?
DEXMETHYLPHENIDATE vs DEXMETHYLPHENIDATE\SERDEXMETHYLPHENIDATE
DEXMETHYLPHENIDATE vs DEXPANTHENOL
DEXMETHYLPHENIDATE vs DEXRAZOXANE
DEXMETHYLPHENIDATE vs DEXTRAN 70\HYPROMELLOSE 2910
DEXMETHYLPHENIDATE vs DEXTROAMPHETAMINE