🇺🇸 Fosrenol (Lanthanum Carbonate) in United States
18 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: 18
Most-reported reactions
- Diarrhoea — 3 reports (16.67%)
- Nausea — 3 reports (16.67%)
- Gastrointestinal Disorder — 2 reports (11.11%)
- Renal Disorder — 2 reports (11.11%)
- Unresponsive To Stimuli — 2 reports (11.11%)
- Vomiting — 2 reports (11.11%)
- Abdominal Pain — 1 report (5.56%)
- Alanine Aminotransferase Increased — 1 report (5.56%)
- Anaphylactic Reaction — 1 report (5.56%)
- Anti-Erythropoietin Antibody Positive — 1 report (5.56%)
Other Nephrology approved in United States
Frequently asked questions
Is Fosrenol (Lanthanum Carbonate) approved in United States?
Fosrenol (Lanthanum Carbonate) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Fosrenol (Lanthanum Carbonate) in United States?
Shire is the originator. The local marketing authorisation holder may differ — check the official source linked above.