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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126303171 | 12630317 | 1 | I | 201607 | 20160801 | 20160808 | 20160808 | EXP | BR-DSJP-DSE-2016-126499 | DAIICHI | 0.00 | Y | 0.00000 | 20160808 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126303171 | 12630317 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/12.5, QD | N | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
126303171 | 12630317 | 2 | SS | METOPROLOL. | METOPROLOL | 1 | 25 MG, QD | 0 | 25 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126303171 | 12630317 | 1 | Hypertension |
126303171 | 12630317 | 2 | Cardiac disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126303171 | 12630317 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126303171 | 12630317 | Arthritis | |
126303171 | 12630317 | Hypertension | |
126303171 | 12630317 | Overdose | |
126303171 | 12630317 | Thrombosis | |
126303171 | 12630317 | Tooth 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 |
---|---|---|---|---|---|---|
126303171 | 12630317 | 1 | 2014 | 0 | ||
126303171 | 12630317 | 2 | 2014 | 0 |