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
122869312 12286931 2 F 2006 20160831 20160420 20160906 EXP CA-PFIZER INC-2016210618 PFIZER 76.00 YR F Y 0.00000 20160906 CN CA CA

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
122869312 12286931 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 20 MG, WEEKLY 11719 20 MG /wk
122869312 12286931 2 SS SULFASALAZINE. SULFASALAZINE 1 1 G, 2X/DAY 7073 1 G BID
122869312 12286931 3 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 400 MG, 1X/DAY 0 400 MG QD
122869312 12286931 4 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 UNK 0
122869312 12286931 5 C WARFARIN WARFARIN 1 UNK 0
122869312 12286931 6 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0
122869312 12286931 7 C FOLIC ACID. FOLIC ACID 1 UNK 0
122869312 12286931 8 C PREDNISONE. PREDNISONE 1 UNK 0
122869312 12286931 9 C CORTISONE CORTISONEHYDROCORTISONE 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122869312 12286931 1 Rheumatoid arthritis
122869312 12286931 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122869312 12286931 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122869312 12286931 Arthralgia
122869312 12286931 Arthropathy
122869312 12286931 Cardiac aneurysm
122869312 12286931 Drug ineffective
122869312 12286931 Joint swelling
122869312 12286931 Pain in extremity

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
122869312 12286931 1 2004 0
122869312 12286931 2 2004 0
122869312 12286931 3 2004 0