🇺🇸 Morphine Sulfate Sustained-Release Tablet in United States
13 US adverse-event reports
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
- Window: 23 April 2025 – 23 April 2026
- Total reports: 13
Most-reported reactions
- Anaemia — 3 reports (23.08%)
- Hypokalaemia — 2 reports (15.38%)
- Acute Kidney Injury — 1 report (7.69%)
- Agranulocytosis — 1 report (7.69%)
- Alanine Aminotransferase Increased — 1 report (7.69%)
- Bacterial Sepsis — 1 report (7.69%)
- Blood Alkaline Phosphatase Increased — 1 report (7.69%)
- Blood Bilirubin Increased — 1 report (7.69%)
- Blood Creatinine Increased — 1 report (7.69%)
- Diarrhoea — 1 report (7.69%)
Other Pain Management approved in United States
Frequently asked questions
Is Morphine Sulfate Sustained-Release Tablet approved in United States?
Morphine Sulfate Sustained-Release Tablet does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Morphine Sulfate Sustained-Release Tablet in United States?
Mundipharma (China) Pharmaceutical Co. Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.