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
127026632 12702663 2 F 20160808 20160923 20160831 20160929 EXP GB-SYMPLMED PHARMACEUTICALS-2016SYMPLMED000309 SYMPLMED PHARMACEUTICALS 0.00 Y 0.00000 20160929 OT 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
127026632 12702663 1 PS PERINDOPRIL ERBUMINE. PERINDOPRIL ERBUMINE 1 Oral 4 MG, QD 24 MG Y U UNKNOWN 20184 4 MG TABLET
127026632 12702663 2 C ENOXAPARIN SODIUM. ENOXAPARIN SODIUM 1 40 MG, QD U UNKNOWN 0 40 MG
127026632 12702663 3 C BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 UNK U UNKNOWN 0
127026632 12702663 4 C FUROSEMIDE. FUROSEMIDE 1 UNK U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127026632 12702663 1 Cardiac failure
127026632 12702663 2 Thrombosis prophylaxis
127026632 12702663 3 Product used for unknown indication
127026632 12702663 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127026632 12702663 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127026632 12702663 Liver function test abnormal

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
127026632 12702663 1 20160803 20160811 0