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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124535242 | 12453524 | 2 | F | 201405 | 20160129 | 20160609 | 20160720 | EXP | US-DSJP-DSU-2015-134190 | DAIICHI | 49.38 | YR | F | Y | 70.75000 | KG | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124535242 | 12453524 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 20/12.5MG, UNK | Y | 21532 | FILM-COATED TABLET | ||||||||
| 124535242 | 12453524 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5MG, UNK | Y | 21532 | FILM-COATED TABLET | ||||||||
| 124535242 | 12453524 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5MG, UNK | Y | 21532 | FILM-COATED TABLET | ||||||||
| 124535242 | 12453524 | 4 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5MG, UNK | Y | 21532 | FILM-COATED TABLET | ||||||||
| 124535242 | 12453524 | 5 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, UNK | Y | 0 | 40 | MG | TABLET | ||||||
| 124535242 | 12453524 | 6 | C | BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | BENAZEPRIL HYDROCHLORIDEHYDROCHLOROTHIAZIDE | 1 | UNK | 0 | |||||||||||
| 124535242 | 12453524 | 7 | C | ADVIL | IBUPROFEN | 1 | UNK | 0 | |||||||||||
| 124535242 | 12453524 | 8 | C | ADVIL | IBUPROFEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124535242 | 12453524 | 1 | Hypertension |
| 124535242 | 12453524 | 5 | Hypertension |
| 124535242 | 12453524 | 6 | Hypertension |
| 124535242 | 12453524 | 7 | Headache |
| 124535242 | 12453524 | 8 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124535242 | 12453524 | OT |
| 124535242 | 12453524 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124535242 | 12453524 | Acute kidney injury | |
| 124535242 | 12453524 | Decreased appetite | |
| 124535242 | 12453524 | Duodenitis | |
| 124535242 | 12453524 | Haematuria | |
| 124535242 | 12453524 | Hepatic function abnormal | |
| 124535242 | 12453524 | Hypotension | |
| 124535242 | 12453524 | Jaundice | |
| 124535242 | 12453524 | Lethargy | |
| 124535242 | 12453524 | Malabsorption |
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 |
|---|---|---|---|---|---|---|
| 124535242 | 12453524 | 1 | 20080126 | 20080225 | 0 | |
| 124535242 | 12453524 | 2 | 20080518 | 20090920 | 0 | |
| 124535242 | 12453524 | 3 | 20100330 | 20131213 | 0 | |
| 124535242 | 12453524 | 4 | 20140127 | 201407 | 0 | |
| 124535242 | 12453524 | 5 | 20140122 | 20140126 | 0 | |
| 124535242 | 12453524 | 6 | 200909 | 201003 | 0 | |
| 124535242 | 12453524 | 7 | 2007 | 0 |