The Safety Rates Drug Report

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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
125378451 12537845 1 I 2005 20150630 20160707 20160707 PER US-DSJP-DSU-2015-120987 DAIICHI 0.00 F Y 76.64000 KG 20160707 MD 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
125378451 12537845 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/12.5 MG, QD 21532 FILM-COATED TABLET QD
125378451 12537845 2 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK 0
125378451 12537845 3 C DEPAKOTE DIVALPROEX SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378451 12537845 1 Hypertension
125378451 12537845 2 Product used for unknown indication
125378451 12537845 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378451 12537845 Depression
125378451 12537845 Dizziness
125378451 12537845 Malabsorption
125378451 12537845 Sleep 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
125378451 12537845 1 200505 201003 0