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
123854863 12385486 3 F 2007 20160627 20160519 20160705 EXP CA-PFIZER INC-2016243508 PFIZER 65.00 YR F Y 0.00000 20160705 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
123854863 12385486 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 25 MG, WEEKLY 2625 MG Y 11719 25 MG /wk
123854863 12385486 2 SS SULFASALAZINE. SULFASALAZINE 1 2 G, UNK 7073 2 G
123854863 12385486 3 C ARAVA LEFLUNOMIDE 1 10 MG, UNK 0 10 MG
123854863 12385486 4 C PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 200 MG, UNK 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123854863 12385486 1 Rheumatoid arthritis
123854863 12385486 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
123854863 12385486 HO
123854863 12385486 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123854863 12385486 Contusion
123854863 12385486 Drug ineffective
123854863 12385486 Fall
123854863 12385486 Oesophageal carcinoma
123854863 12385486 Peripheral swelling
123854863 12385486 Upper limb fracture

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
123854863 12385486 1 20050507 20070507 0
123854863 12385486 2 20091102 0
123854863 12385486 3 20141201 20150203 0
123854863 12385486 4 20120420 20160502 0