🇺🇸 Lactobacillus plantarum in United States

33 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.

Most-reported reactions

  1. Pyrexia — 5 reports (15.15%)
  2. Stress — 4 reports (12.12%)
  3. Arthralgia — 3 reports (9.09%)
  4. Condition Aggravated — 3 reports (9.09%)
  5. Cough — 3 reports (9.09%)
  6. Crohn^S Disease — 3 reports (9.09%)
  7. Diarrhoea — 3 reports (9.09%)
  8. Dizziness — 3 reports (9.09%)
  9. Drug Ineffective — 3 reports (9.09%)
  10. Fatigue — 3 reports (9.09%)

Source database →

Other Gastroenterology approved in United States

Frequently asked questions

Is Lactobacillus plantarum approved in United States?

Lactobacillus plantarum does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Lactobacillus plantarum in United States?

Shenzhen People's Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.