The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126172771 12617277 1 I 20160630 20160726 20160803 20160803 EXP FR-ASTRAZENECA-2016SE81897 ASTRAZENECA 11752.00 DY F Y 0.00000 20160803 MD FR FR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126172771 12617277 1 PS INEXIUM ESOMEPRAZOLE 1 Oral 1 DF U U 21153 1 DF QD
126172771 12617277 2 SS CELEBREX CELECOXIB 1 Oral 200 MG Y U 0 200 MG QD
126172771 12617277 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral 1 DF Y U 0 1 DF QD
126172771 12617277 4 C SPOTOF TRANEXAMIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126172771 12617277 1 Prophylaxis against gastrointestinal ulcer
126172771 12617277 2 Rheumatoid arthritis
126172771 12617277 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126172771 12617277 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126172771 12617277 Headache
126172771 12617277 Hyperthermia
126172771 12617277 Meningeal disorder
126172771 12617277 Musculoskeletal stiffness
126172771 12617277 Photophobia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126172771 12617277 1 20160629 0
126172771 12617277 2 20160629 20160629 0
126172771 12617277 3 20160629 20160629 0