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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125999371 | 12599937 | 1 | I | 20160720 | 20160727 | 20160727 | PER | US-009507513-1607USA008135 | MERCK | 71.00 | YR | M | Y | 0.00000 | 20160727 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125999371 | 12599937 | 1 | PS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | UNK | U | 20386 | TABLET | ||||||||
| 125999371 | 12599937 | 2 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | U | 0 | |||||||||||
| 125999371 | 12599937 | 3 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 125999371 | 12599937 | 4 | SS | ATORVASTATIN | ATORVASTATIN | 1 | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125999371 | 12599937 | Confusional state | |
| 125999371 | 12599937 | Fatigue | |
| 125999371 | 12599937 | Neuropathy peripheral | |
| 125999371 | 12599937 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 125999371 | 12599937 | 1 | 2013 | 0 |