The Safety Rates Drug Report

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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
115903045 11590304 5 F 2014 20160712 20151002 20160720 EXP CA-PFIZER INC-2015323993 PFIZER 0.00 E M Y 0.00000 20160720 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
115903045 11590304 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 11719
115903045 11590304 2 SS ENBREL ETANERCEPT 1 Subcutaneous UNK Y 0
115903045 11590304 3 SS SULFASALAZINE. SULFASALAZINE 1 UNK Y 7073
115903045 11590304 4 SS GOLD GOLD 1 UNK 0
115903045 11590304 5 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK Y 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115903045 11590304 1 Rheumatoid arthritis
115903045 11590304 2 Rheumatoid arthritis
115903045 11590304 3 Rheumatoid arthritis
115903045 11590304 4 Rheumatoid arthritis
115903045 11590304 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
115903045 11590304 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115903045 11590304 Acute kidney injury
115903045 11590304 Drug effect decreased

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
115903045 11590304 2 2013 0