🇺🇸 cefdinir (Omnicef) in United States

10 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. Abortion Missed — 1 report (10%)
  2. Computerised Tomogram Thorax Abnormal — 1 report (10%)
  3. Cytomegalovirus Viraemia — 1 report (10%)
  4. Device Related Infection — 1 report (10%)
  5. Klebsiella Bacteraemia — 1 report (10%)
  6. Lower Respiratory Tract Infection — 1 report (10%)
  7. Lung Infiltration — 1 report (10%)
  8. Maternal Exposure During Pregnancy — 1 report (10%)
  9. Pneumonia — 1 report (10%)
  10. Pneumonia Bacterial — 1 report (10%)

Source database →

Other Infectious Disease approved in United States

Frequently asked questions

Is cefdinir (Omnicef) approved in United States?

cefdinir (Omnicef) does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for cefdinir (Omnicef) in United States?

Abbott is the originator. The local marketing authorisation holder may differ — check the official source linked above.