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
123719932 12371993 2 F 20160425 20160819 20160516 20160824 EXP DE-SA-2016SA094358 AVENTIS 64.00 YR A M Y 90.00000 KG 20160824 CN DE DE

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
123719932 12371993 1 PS CLEXANE ENOXAPARIN SODIUM 1 Subcutaneous STOP DATE 2016 UNKNOWN 20164 .4 ML SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123719932 12371993 1 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
123719932 12371993 DE
123719932 12371993 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123719932 12371993 Cough
123719932 12371993 Deep vein thrombosis
123719932 12371993 Drug ineffective
123719932 12371993 Pain in extremity
123719932 12371993 Peripheral swelling
123719932 12371993 Pulmonary embolism

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
123719932 12371993 1 20160229 20160425 0