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
126764472 12676447 2 F 20160301 20160817 20160823 20160825 EXP GB-ASTRAZENECA-2016SE88910 ASTRAZENECA 84.00 YR M Y 0.00000 20160825 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
126764472 12676447 1 PS CANDESARTAN CILEXETIL. CANDESARTAN CILEXETIL 1 Oral TEVA, 4 MG UKNOWN 20838 TABLET
126764472 12676447 2 SS CANDESARTAN CILEXETIL. CANDESARTAN CILEXETIL 1 Oral 4.0MG UNKNOWN 20838 4 MG TABLET
126764472 12676447 3 SS CANDESARTAN CILEXETIL. CANDESARTAN CILEXETIL 1 Unknown MYLAN BRAND OF CANDESARTAN UNKNOWN 20838
126764472 12676447 4 C ASPIRIN. ASPIRIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126764472 12676447 1 Product used for unknown indication
126764472 12676447 2 Product used for unknown indication
126764472 12676447 3 Product used for unknown indication
126764472 12676447 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126764472 12676447 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126764472 12676447 Abdominal discomfort
126764472 12676447 Diarrhoea
126764472 12676447 Transient ischaemic attack

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found