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
127226261 12722626 1 I 2009 20160831 20160907 20160907 EXP CA-SA-2016SA163126 AVENTIS 35.00 YR A F Y 0.00000 20160907 MD 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
127226261 12722626 1 PS LEFLUNOMIDE. LEFLUNOMIDE 1 Oral N UNKNOWN 20905
127226261 12722626 2 SS SULFASALAZINE. SULFASALAZINE 1 Oral N UNKNOWN 0
127226261 12722626 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral N UNKNOWN 0 1500 MG BID
127226261 12722626 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous N UNKNOWN 0 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127226261 12722626 1 Rheumatoid arthritis
127226261 12722626 2 Rheumatoid arthritis
127226261 12722626 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127226261 12722626 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127226261 12722626 Alopecia
127226261 12722626 Drug intolerance
127226261 12722626 Hepatic enzyme increased
127226261 12722626 Intervertebral disc protrusion
127226261 12722626 Iritis
127226261 12722626 Pneumonia
127226261 12722626 Walking disability

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
127226261 12722626 1 20160105 20160120 0
127226261 12722626 2 200704 0
127226261 12722626 3 201504 201604 0
127226261 12722626 4 201509 201604 0