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
126411111 12641111 1 I 20160630 20160802 20160810 20160810 EXP US-ASTRAZENECA-2016SE83219 ASTRAZENECA 32.00 YR F Y 0.00000 20160810 OT 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
126411111 12641111 1 PS INEXIUM ESOMEPRAZOLE 1 Oral 2 DF U U 21153 1 DF QD
126411111 12641111 2 SS CELEBREX CELECOXIB 1 Oral 200 MG Y U 0 200 MG CAPSULE, HARD QD
126411111 12641111 3 SS CELEBREX CELECOXIB 1 Oral 200 MG Y U 0 200 MG CAPSULE, HARD QD
126411111 12641111 4 SS SULFASALAZINE. SULFASALAZINE 1 Oral 1 DF Y U 0 1 DF MODIFIED-RELEASE TABLET QD
126411111 12641111 5 C SPOTOF TRANEXAMIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126411111 12641111 1 Prophylaxis against gastrointestinal ulcer
126411111 12641111 2 Arthritis
126411111 12641111 3 Rheumatoid arthritis
126411111 12641111 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126411111 12641111 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126411111 12641111 Headache
126411111 12641111 Hyperthermia
126411111 12641111 Meningeal disorder
126411111 12641111 Musculoskeletal stiffness
126411111 12641111 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
126411111 12641111 1 20160629 0
126411111 12641111 2 20160629 20160629 0
126411111 12641111 3 20160629 20160629 0
126411111 12641111 4 20160629 20160629 0