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
127026481 12702648 1 I 20081201 20081204 20160831 20160831 EXP UA-PFIZER INC-2008150529 PFIZER 77.00 YR F Y 72.00000 KG 20160831 MD UA UA

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
127026481 12702648 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK Y 18989 TABLET
127026481 12702648 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral UNK 0
127026481 12702648 3 C NEBILET NEBIVOLOL 1 Oral UNK 0
127026481 12702648 4 C CARDIOMAGNYL ASPIRINMAGNESIUM HYDROXIDE 1 Oral UNK 0
127026481 12702648 5 C ZOCOR SIMVASTATIN 1 Oral UNK 0
127026481 12702648 6 C VEROSPIRON SPIRONOLACTONE 1 Oral UNK 0
127026481 12702648 7 C SUPRADYN ASCORBIC ACIDMINERALSVITAMINS 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127026481 12702648 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127026481 12702648 HO
127026481 12702648 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127026481 12702648 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
127026481 12702648 1 20081030 20081203 0
127026481 12702648 2 20081003 20081203 0
127026481 12702648 3 2006 0
127026481 12702648 4 2006 0
127026481 12702648 5 2006 0
127026481 12702648 6 2006 20081203 0
127026481 12702648 7 20081003 20081127 0