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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEXTROAMPHETAMINE Cause Device issue? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Device issue have been filed in association with DEXTROAMPHETAMINE (Zenzedi). This represents 1.2% of all adverse event reports for DEXTROAMPHETAMINE.

26
Reports of Device issue with DEXTROAMPHETAMINE
1.2%
of all DEXTROAMPHETAMINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device issue From DEXTROAMPHETAMINE?

Of the 26 reports.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEXTROAMPHETAMINE. However, 26 reports have been filed with the FAERS database.

What Other Side Effects Does DEXTROAMPHETAMINE Cause?

Drug ineffective (513) Fatigue (170) Anxiety (169) Product substitution issue (163) Headache (145) Nausea (130) Off label use (121) Somnolence (110) Feeling abnormal (108) Product availability issue (106)

What Other Drugs Cause Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which DEXTROAMPHETAMINE Alternatives Have Lower Device issue Risk?

DEXTROAMPHETAMINE vs DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE AND AMPHETAMINE DEXTROAMPHETAMINE vs DEXTROMETHORPHAN DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN\PHENYLEPHRINE

Related Pages

DEXTROAMPHETAMINE Full Profile All Device issue Reports All Drugs Causing Device issue DEXTROAMPHETAMINE Demographics