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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124130062 | 12413006 | 2 | F | 2010 | 20160809 | 20160527 | 20160816 | EXP | US-DSJP-DSU-2016-117904 | DAIICHI | 0.00 | Y | 0.00000 | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124130062 | 12413006 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 20/12.5 MG, UNK | Y | 21532 | 1 | DF | FILM-COATED TABLET | |||||||
| 124130062 | 12413006 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/12.5 MG, UNK | Y | 21532 | 1 | DF | FILM-COATED TABLET | |||||||
| 124130062 | 12413006 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/25 MG, QD | Y | 21532 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 124130062 | 12413006 | 4 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 10 MG, QD | 0 | 10 | MG | QD | |||||||
| 124130062 | 12413006 | 5 | C | FISH OIL | FISH OIL | 1 | Oral | UNK UNK, QD | 0 | TABLET | QD | ||||||||
| 124130062 | 12413006 | 6 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Oral | 325 MG, QD | 0 | 325 | MG | QD | |||||||
| 124130062 | 12413006 | 7 | C | MVI /01825701/ | VITAMINS | 1 | Oral | UNK UNK, QD | 0 | TABLET | QD | ||||||||
| 124130062 | 12413006 | 8 | C | GLUCOSAMINE | GLUCOSAMINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124130062 | 12413006 | 1 | Hypertension |
| 124130062 | 12413006 | 4 | Product used for unknown indication |
| 124130062 | 12413006 | 5 | Product used for unknown indication |
| 124130062 | 12413006 | 6 | Product used for unknown indication |
| 124130062 | 12413006 | 7 | Product used for unknown indication |
| 124130062 | 12413006 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124130062 | 12413006 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124130062 | 12413006 | Acute kidney injury | |
| 124130062 | 12413006 | Anaemia | |
| 124130062 | 12413006 | Chills | |
| 124130062 | 12413006 | Dyspnoea exertional | |
| 124130062 | 12413006 | Gastrointestinal haemorrhage | |
| 124130062 | 12413006 | Gluten sensitivity | |
| 124130062 | 12413006 | Hypotension | |
| 124130062 | 12413006 | Lactose intolerance | |
| 124130062 | 12413006 | 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 |
|---|---|---|---|---|---|---|
| 124130062 | 12413006 | 1 | 20080111 | 20110125 | 0 | |
| 124130062 | 12413006 | 2 | 201102 | 201103 | 0 | |
| 124130062 | 12413006 | 3 | 20110407 | 0 |