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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117928207 | 11792820 | 7 | F | 201302 | 20160912 | 20151202 | 20160919 | EXP | US-DSJP-DSU-2015-122259 | DAIICHI | 0.00 | Y | 0.00000 | 20160919 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117928207 | 11792820 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | Y | 21286 | 40 | MG | TABLET | QD | |||||
117928207 | 11792820 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 MG,QD | Y | 21286 | 20 | MG | TABLET | QD | ||||||
117928207 | 11792820 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | UNK | U | 0 | FILM-COATED TABLET | |||||||||
117928207 | 11792820 | 4 | C | HYDRALAZINE | HYDRALAZINE HYDROCHLORIDE | 1 | 2 DF, QD | 0 | 2 | DF | TABLET | QD | |||||||
117928207 | 11792820 | 5 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 1 DF, QD | 0 | 1 | DF | TABLET | QD | |||||||
117928207 | 11792820 | 6 | C | CLONIDINE. | CLONIDINE | 1 | 0.1 MG, TID | 0 | .1 | MG | TID | ||||||||
117928207 | 11792820 | 7 | C | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 100 MG, ONCE EVERY 12HR | 0 | 100 | MG | Q12H |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117928207 | 11792820 | 1 | Hypertension |
117928207 | 11792820 | 3 | Product used for unknown indication |
117928207 | 11792820 | 4 | Product used for unknown indication |
117928207 | 11792820 | 5 | Product used for unknown indication |
117928207 | 11792820 | 6 | Product used for unknown indication |
117928207 | 11792820 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
117928207 | 11792820 | OT |
117928207 | 11792820 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117928207 | 11792820 | Acute kidney injury | |
117928207 | 11792820 | Anaemia | |
117928207 | 11792820 | Chronic kidney disease | |
117928207 | 11792820 | Clostridium difficile infection | |
117928207 | 11792820 | Coeliac disease | |
117928207 | 11792820 | Confusional state | |
117928207 | 11792820 | Constipation | |
117928207 | 11792820 | Depression | |
117928207 | 11792820 | Diverticulum | |
117928207 | 11792820 | Dizziness | |
117928207 | 11792820 | Gastrointestinal melanosis | |
117928207 | 11792820 | Haemorrhoids | |
117928207 | 11792820 | Helicobacter gastritis | |
117928207 | 11792820 | Ileus | |
117928207 | 11792820 | Malabsorption | |
117928207 | 11792820 | Obstruction | |
117928207 | 11792820 | Pancreatitis | |
117928207 | 11792820 | Presyncope | |
117928207 | 11792820 | Proteinuria |
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 |
---|---|---|---|---|---|---|
117928207 | 11792820 | 1 | 2012 | 201309 | 0 | |
117928207 | 11792820 | 4 | 201302 | 0 | ||
117928207 | 11792820 | 5 | 201302 | 0 | ||
117928207 | 11792820 | 6 | 201302 | 0 | ||
117928207 | 11792820 | 7 | 201302 | 0 |