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
125284471 12528447 1 I 20160602 20160629 20160705 20160705 EXP FR-DSJP-DSE-2016-122041 DAIICHI 0.00 Y 0.00000 20160705 MD FR FR

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
125284471 12528447 1 PS SEVIKAR 40 mg/ 5 mg AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 Oral 40/5 MG, QD Y 22100 1 DF TABLET QD
125284471 12528447 2 SS ALLOPURINOL. ALLOPURINOL 1 Oral 1 DF, QD 0 1 DF QD
125284471 12528447 3 SS DIFFU K POTASSIUM CHLORIDE 1 Oral 2 DF, QD 0 2 DF QD
125284471 12528447 4 SS TAHOR ATORVASTATIN CALCIUM 1 Oral 20 MG, QD 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125284471 12528447 1 Hypertension
125284471 12528447 2 Product used for unknown indication
125284471 12528447 3 Product used for unknown indication
125284471 12528447 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125284471 12528447 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125284471 12528447 Acute kidney injury
125284471 12528447 Diarrhoea
125284471 12528447 Dyspnoea
125284471 12528447 Metabolic acidosis

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
125284471 12528447 1 20160614 0
125284471 12528447 2 201606 0
125284471 12528447 4 201606 0