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
126146141 12614614 1 I 20160630 20160726 20160802 20160802 EXP FR-PFIZER INC-2016361961 PFIZER 32.00 YR F Y 0.00000 20160802 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
126146141 12614614 1 PS CELEBREX CELECOXIB 1 Oral 200 MG, 1X/DAY 200 MG Y 20998 200 MG CAPSULE, HARD QD
126146141 12614614 2 SS CELEBREX CELECOXIB 1 200 MG Y 20998 CAPSULE, HARD
126146141 12614614 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral 1 DF, 1X/DAY 1 DF Y 7073 1 DF MODIFIED-RELEASE TABLET QD
126146141 12614614 4 SS Inexium ESOMEPRAZOLE 1 Oral 1 DF, 1X/DAY U 0 1 DF QD
126146141 12614614 5 C SPOTOF TRANEXAMIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126146141 12614614 1 Arthritis
126146141 12614614 2 Rheumatoid arthritis
126146141 12614614 3 Rheumatoid arthritis
126146141 12614614 4 Prophylaxis against gastrointestinal ulcer

Outcome of event

Event ID CASEID OUTC COD
126146141 12614614 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126146141 12614614 Headache
126146141 12614614 Hyperthermia
126146141 12614614 Meningeal disorder
126146141 12614614 Musculoskeletal stiffness
126146141 12614614 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
126146141 12614614 1 20160629 20160629 0
126146141 12614614 3 20160629 20160629 0
126146141 12614614 4 20160629 0