pharmacopeia

Strontium

US-FDASourced from openFDA
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Approval history

Sourced from openFDA
  • Aug 6, 2013NDANDA202342Belcher

FAERS reports

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Reference statistics only. FAERS reports are voluntarily submitted and are not incidence rates, safety signals, or causal evidence. Counts reflect reporting volume — how often a reaction was reported, not how often it occurs. For decision-grade use, consult openFDA and the FAERS Public Dashboard directly.
1,536 total reports matchedLatest report Share = reports listing the reaction ÷ total matched reports. Rows can sum to >100% because a single report often lists multiple reactions.
  1. 1Nausea16511%
  2. 2Vomiting1368.9%
  3. 3Diarrhoea1308.5%
  4. 4Fatigue1268.2%
  5. 5Pain1087.0%
  6. 6Dehydration1066.9%
  7. 7Dyspnoea996.4%
  8. 8Pyrexia915.9%
  9. 9Asthenia905.9%
  10. 10Pneumonia775.0%
  11. 11Headache764.9%
  12. 12Dizziness744.8%
  13. 13Weight Decreased704.6%
  14. 14Dysphagia664.3%
  15. 15Fall614.0%

Literature

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Recent PubMed references pinned to Strontium as a MeSH major topic. Citations link to pubmed.ncbi.nlm.nih.gov.

Clinical trials

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The 10 most recently updated of 47 ClinicalTrials.gov registrations naming Strontium as an intervention. Registration is not evidence of efficacy or safety — reference crosswalk only.

Note. Data for strontium is illustrative MVP content compiled from public sources. pharmacopeia is for educational and informational use only and is not a substitute for professional medical advice.

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