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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124537202 | 12453720 | 2 | F | 2004 | 20160520 | 20160609 | 20160720 | PER | US-DSJP-DSU-2015-133238 | DAIICHI | 0.00 | M | Y | 103.00000 | KG | 20160718 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124537202 | 12453720 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40MG/25MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
| 124537202 | 12453720 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 20MG/12.5MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
| 124537202 | 12453720 | 3 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 40 MG, UNK | U | 0 | 40 | MG | TABLET | |||||||
| 124537202 | 12453720 | 4 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 MG, UNK | U | 0 | 20 | MG | TABLET | |||||||
| 124537202 | 12453720 | 5 | C | NORVASC | AMLODIPINE BESYLATE | 1 | 10 MG, QD | 0 | 10 | MG | QD | ||||||||
| 124537202 | 12453720 | 6 | C | POTASSIUM CHLORIDE. | POTASSIUM CHLORIDE | 1 | 10 MEQ, UNK | 0 | 10 | MEQ | CAPSULE | ||||||||
| 124537202 | 12453720 | 7 | C | CLONIDINE. | CLONIDINE | 1 | 0.1 MG, AS NEEDED | 0 | .1 | MG | TABLET | ||||||||
| 124537202 | 12453720 | 8 | C | VALSARTAN. | VALSARTAN | 1 | Oral | 320MG/25MG, QD | 0 | 1 | DF | QD | |||||||
| 124537202 | 12453720 | 9 | C | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124537202 | 12453720 | 1 | Hypertension |
| 124537202 | 12453720 | 3 | Hypertension |
| 124537202 | 12453720 | 5 | Hypertension |
| 124537202 | 12453720 | 6 | Blood potassium decreased |
| 124537202 | 12453720 | 7 | Hypertension |
| 124537202 | 12453720 | 8 | Product used for unknown indication |
| 124537202 | 12453720 | 9 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124537202 | 12453720 | Anaemia | |
| 124537202 | 12453720 | Dizziness | |
| 124537202 | 12453720 | Gastrointestinal haemorrhage | |
| 124537202 | 12453720 | Malabsorption | |
| 124537202 | 12453720 | Off label use |
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 |
|---|---|---|---|---|---|---|
| 124537202 | 12453720 | 1 | 200401 | 201107 | 0 | |
| 124537202 | 12453720 | 2 | 200401 | 201107 | 0 | |
| 124537202 | 12453720 | 3 | 200312 | 0 |