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
127640891 12764089 1 I 201603 20160914 20160920 20160920 EXP FR-SA-2016SA171336 AVENTIS 90.00 YR E F Y 71.50000 KG 20160920 OT FR FR

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
127640891 12764089 1 PS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous D UNKNOWN 20164 INJECTION
127640891 12764089 2 SS PREVISCAN FLUINDIONE 1 Oral D UNKNOWN 0 TABLET
127640891 12764089 3 SS PREVISCAN FLUINDIONE 1 Oral D UNKNOWN 0 TABLET
127640891 12764089 4 C FUROSEMIDE. FUROSEMIDE 1 Oral 0 750 MG QD
127640891 12764089 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0 50 MG QD
127640891 12764089 6 C DIFFU K POTASSIUM CHLORIDE 1 Oral 0 1200 MG QD
127640891 12764089 7 C ALLOPURINOL. ALLOPURINOL 1 Oral 0
127640891 12764089 8 C LEVOTHYROX LEVOTHYROXINE 1 Oral 0 1 DF QD
127640891 12764089 9 C DOLIPRANE ACETAMINOPHEN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127640891 12764089 2 Atrial fibrillation
127640891 12764089 3 International normalised ratio abnormal

Outcome of event

Event ID CASEID OUTC COD
127640891 12764089 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127640891 12764089 Anaemia
127640891 12764089 International normalised ratio increased
127640891 12764089 Melaena
127640891 12764089 Muscle haemorrhage
127640891 12764089 Overdose

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
127640891 12764089 1 20160216 201603 0
127640891 12764089 2 20160216 0
127640891 12764089 3 20160216 0