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
126004232 12600423 2 F 2011 20160804 20160727 20160811 EXP BR-ASTRAZENECA-2016SE79301 ASTRAZENECA 75.00 YR M Y 70.00000 KG 20160811 CN BR BR

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
126004232 12600423 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral Y U 20838 16 MG TABLET QD
126004232 12600423 2 SS ATACAND CANDESARTAN CILEXETIL 1 Oral Y U 20838 .5 DF TABLET QD
126004232 12600423 3 SS SELOZOK METOPROLOL SUCCINATE 1 Oral 146100 MG 0 100 MG MODIFIED-RELEASE TABLET QD
126004232 12600423 4 C SIMVASTATIN. SIMVASTATIN 1 0 .5 DF TABLET QD
126004232 12600423 5 C ASA INFANTIL ASPIRIN 1 DAILY 0
126004232 12600423 6 C UNKNOWN UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126004232 12600423 1 Blood pressure abnormal
126004232 12600423 2 Blood pressure abnormal
126004232 12600423 3 Blood pressure abnormal
126004232 12600423 6 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
126004232 12600423 DS
126004232 12600423 HO
126004232 12600423 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126004232 12600423 Cerebrovascular accident
126004232 12600423 Off label use
126004232 12600423 Pulmonary embolism
126004232 12600423 Spinal disorder

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
126004232 12600423 1 2007 0
126004232 12600423 3 2007 0
126004232 12600423 4 2007 0
126004232 12600423 5 2007 0
126004232 12600423 6 2011 0