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
68786063 6878606 3 F 20080915 20160824 20090112 20160830 EXP US-PFIZER INC-2008079717 PFIZER 61.00 YR F Y 87.98000 KG 20160830 MD US US

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
68786063 6878606 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK Y 18989 TABLET
68786063 6878606 2 SS IBUPROFEN. IBUPROFEN 1 Y 18989 TABLET
68786063 6878606 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 20 MG, UNK 0 20 MG
68786063 6878606 4 C METHOTREXATE. METHOTREXATE 1 Oral UNK 0
68786063 6878606 5 C PRINZIDE HYDROCHLOROTHIAZIDELISINOPRIL 1 Oral UNK 0
68786063 6878606 6 C FOLIC ACID. FOLIC ACID 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
68786063 6878606 1 Osteoarthritis
68786063 6878606 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
68786063 6878606 HO
68786063 6878606 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
68786063 6878606 Renal failure

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
68786063 6878606 1 20080815 20080915 0
68786063 6878606 3 20080814 20080915 0
68786063 6878606 4 19800101 20080915 0
68786063 6878606 5 20030101 20080915 0
68786063 6878606 6 19800101 20080915 0