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
127294891 12729489 1 I 20160525 20160831 20160909 20160909 EXP GB-SA-2016SA161994 AVENTIS 73.00 YR E F Y 0.00000 20160909 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
127294891 12729489 1 PS INDAPAMIDE. INDAPAMIDE 1 Unknown Y UNK 18538
127294891 12729489 2 SS ATENOLOL. ATENOLOL 1 Unknown DOSE: 1 UNITS UNSPECIFIED UNK 0 50 MG TABLET QD
127294891 12729489 3 SS ATENOLOL. ATENOLOL 1 Unknown DOSE: 1 UNITS UNSPECIFIED BPQ084040 0 50 MG TABLET QD
127294891 12729489 4 C ALENDRONIC ACID ALENDRONIC ACID 1 0 1 DF /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127294891 12729489 1 Hypertension
127294891 12729489 2 Hypertension
127294891 12729489 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127294891 12729489 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127294891 12729489 Hypersensitivity
127294891 12729489 Swollen tongue

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
127294891 12729489 1 201511 20160702 0
127294891 12729489 2 201605 0
127294891 12729489 3 201605 0