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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112556815 | 11255681 | 5 | F | 201502 | 20160829 | 20150709 | 20160831 | EXP | US-DSJP-DSU-2015-120672 | DAIICHI | 0.00 | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112556815 | 11255681 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 TO 40 MG, QD, 1.5 TABLETS PER DAY | Y | 21286 | 1 | DF | TABLET | QD | ||||||
| 112556815 | 11255681 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | Y | 21286 | 40 | MG | TABLET | QD | |||||
| 112556815 | 11255681 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40MG/12.5 MG, QD | Y | 0 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 112556815 | 11255681 | 4 | C | HYDROCODONE | HYDROCODONE | 1 | Oral | 1 DF, PRN | 0 | 1 | DF | TABLET | |||||||
| 112556815 | 11255681 | 5 | C | TYLENOL | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112556815 | 11255681 | 1 | Hypertension |
| 112556815 | 11255681 | 3 | Hypertension |
| 112556815 | 11255681 | 4 | Pain |
| 112556815 | 11255681 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 112556815 | 11255681 | OT |
| 112556815 | 11255681 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112556815 | 11255681 | Acute kidney injury | |
| 112556815 | 11255681 | Anaemia | |
| 112556815 | 11255681 | Depression | |
| 112556815 | 11255681 | Dizziness | |
| 112556815 | 11255681 | Dyspnoea | |
| 112556815 | 11255681 | End stage renal disease | |
| 112556815 | 11255681 | Gastrooesophageal reflux disease | |
| 112556815 | 11255681 | Gouty arthritis | |
| 112556815 | 11255681 | Hiatus hernia | |
| 112556815 | 11255681 | Irritable bowel syndrome | |
| 112556815 | 11255681 | 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 |
|---|---|---|---|---|---|---|
| 112556815 | 11255681 | 1 | 20090206 | 201504 | 0 | |
| 112556815 | 11255681 | 3 | 2002 | 20090204 | 0 | |
| 112556815 | 11255681 | 4 | 2005 | 0 | ||
| 112556815 | 11255681 | 5 | 2005 | 0 |