Does HYDROMORPHONE Cause Product dose omission issue? 87 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 87 reports of Product dose omission issue have been filed in association with HYDROMORPHONE (Hydromorphone Hydrochloride). This represents 0.1% of all adverse event reports for HYDROMORPHONE.
87
Reports of Product dose omission issue with HYDROMORPHONE
0.1%
of all HYDROMORPHONE reports
29
Deaths
55
Hospitalizations
How Dangerous Is Product dose omission issue From HYDROMORPHONE?
Of the 87 reports, 29 (33.3%) resulted in death, 55 (63.2%) required hospitalization, and 29 (33.3%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROMORPHONE. However, 87 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROMORPHONE Cause?
Drug dependence (39,714)
Overdose (25,322)
Pain (21,325)
Emotional distress (18,260)
Death (15,276)
Drug withdrawal syndrome (14,834)
Toxicity to various agents (10,769)
Drug abuse (3,999)
Drug ineffective (3,562)
Drug withdrawal syndrome neonatal (3,333)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which HYDROMORPHONE Alternatives Have Lower Product dose omission issue Risk?
HYDROMORPHONE vs HYDROQUINONE
HYDROMORPHONE vs HYDROXOCOBALAMIN
HYDROMORPHONE vs HYDROXYCHLOROQUINE
HYDROMORPHONE vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROMORPHONE vs HYDROXYETHYL STARCH 130/0.4