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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 APOMORPHINE Cause Product administration interrupted? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration interrupted have been filed in association with APOMORPHINE (apomorphine hydrocloride). This represents 0.1% of all adverse event reports for APOMORPHINE.

5
Reports of Product administration interrupted with APOMORPHINE
0.1%
of all APOMORPHINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product administration interrupted From APOMORPHINE?

Of the 5 reports.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APOMORPHINE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does APOMORPHINE Cause?

Nausea (2,014) Somnolence (1,403) Dizziness (1,234) Blood pressure decreased (633) Vomiting (609) Fall (555) Yawning (489) Fatigue (487) Hyperhidrosis (431) Drug ineffective (403)

What Other Drugs Cause Product administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which APOMORPHINE Alternatives Have Lower Product administration interrupted Risk?

APOMORPHINE vs APRACLONIDINE APOMORPHINE vs APREMILAST APOMORPHINE vs APREPITANT APOMORPHINE vs APROTININ APOMORPHINE vs ARANESP

Related Pages

APOMORPHINE Full Profile All Product administration interrupted Reports All Drugs Causing Product administration interrupted APOMORPHINE Demographics