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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 NALDEMEDINE Cause Product packaging quantity issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product packaging quantity issue have been filed in association with NALDEMEDINE (SYMPROIC). This represents 1.3% of all adverse event reports for NALDEMEDINE.

9
Reports of Product packaging quantity issue with NALDEMEDINE
1.3%
of all NALDEMEDINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product packaging quantity issue From NALDEMEDINE?

Of the 9 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 NALDEMEDINE. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does NALDEMEDINE Cause?

Diarrhoea (144) Drug ineffective (92) Abdominal pain (68) Constipation (47) Nausea (42) Death (28) Malignant neoplasm progression (27) Vomiting (27) Drug withdrawal syndrome (24) Neoplasm malignant (24)

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 NALDEMEDINE Alternatives Have Lower Product packaging quantity issue Risk?

NALDEMEDINE vs NALMEFENE NALDEMEDINE vs NALOXEGOL OXALATE NALDEMEDINE vs NALOXONE NALDEMEDINE vs NALOXONE\OXYCODONE NALDEMEDINE vs NALOXONE\TILIDINE

Related Pages

NALDEMEDINE Full Profile All Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue NALDEMEDINE Demographics