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
125971631 12597163 1 I 20160520 20160715 20160727 20160727 EXP GB-MHRA-EYC 00142336 GB-TEVA-678323ACC TEVA 74.00 YR M Y 71.66000 KG 20160727 CN GB GB

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
125971631 12597163 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1500 MILLIGRAM DAILY; 10500 MG N U 74124 750 MG BID
125971631 12597163 2 C DICLOFLEX 2 75 MILLIGRAM DAILY; 0 75 MG QD
125971631 12597163 3 C ELIQUIS APIXABAN 1 5 MILLIGRAM DAILY; 0 2.5 MG BID
125971631 12597163 4 C OMEPRAZOLE. OMEPRAZOLE 1 20 MILLIGRAM DAILY; 0 20 MG QD
125971631 12597163 5 C TAMSULOSIN TAMSULOSIN 1 400 MICROGRAM DAILY; 0 400 UG CAPSULE, HARD QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125971631 12597163 1 Lung infection

Outcome of event

Event ID CASEID OUTC COD
125971631 12597163 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125971631 12597163 Pain
125971631 12597163 Peripheral swelling
125971631 12597163 Swelling face

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
125971631 12597163 1 20160513 20160524 0