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
127200481 12720048 1 I 2016 20160812 20160907 20160907 PER US-009507513-1608USA007565 MERCK 0.00 F Y 63.50000 KG 20160907 CN US US

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
127200481 12720048 1 PS PRINIVIL LISINOPRIL 1 Oral UNK Y 19558 TABLET
127200481 12720048 2 SS NORVASK AMLODIPINE BESYLATE 1 Oral 5 MG, QD Y 0 5 MG QD
127200481 12720048 3 SS NORVASK AMLODIPINE BESYLATE 1 Oral 10 MG, QD Y 0 10 MG QD
127200481 12720048 4 C PREDNISONE. PREDNISONE 1 Oral UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127200481 12720048 1 Blood pressure abnormal
127200481 12720048 2 Blood pressure abnormal
127200481 12720048 4 Arthropathy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127200481 12720048 Burning sensation
127200481 12720048 Erythema
127200481 12720048 Joint swelling
127200481 12720048 Oedema
127200481 12720048 Peripheral swelling
127200481 12720048 Rash erythematous
127200481 12720048 Renal 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
127200481 12720048 1 201607 0
127200481 12720048 2 2016 201607 0
127200481 12720048 3 201607 20160805 0