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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120901804 | 12090180 | 4 | F | 200905 | 20160815 | 20160218 | 20160822 | EXP | US-DSJP-DSU-2016-105663 | DAIICHI | 0.00 | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120901804 | 12090180 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 MG, UNK | 3560 | MG | U | 21286 | 20 | MG | TABLET | |||||
| 120901804 | 12090180 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | 3560 | MG | U | 21286 | 40 | MG | TABLET | QD | |||
| 120901804 | 12090180 | 3 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 40 MG, QD | 0 | 40 | MG | QD | |||||||
| 120901804 | 12090180 | 4 | C | ATENOLOL. | ATENOLOL | 1 | Oral | 50 MG, QD | 0 | 50 | MG | QD | |||||||
| 120901804 | 12090180 | 5 | C | OXYCODONE | OXYCODONE | 1 | Oral | 5/325 MG, UNK | 0 | 1 | DF | ||||||||
| 120901804 | 12090180 | 6 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | Oral | 0.25 MG, TID | 0 | .25 | MG | TID | |||||||
| 120901804 | 12090180 | 7 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | 0 | ||||||||||||
| 120901804 | 12090180 | 8 | C | NICOTINE TRANSDERMAL SYSTEM | NICOTINE | 1 | 21 MG, QD | 0 | 21 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120901804 | 12090180 | 1 | Hypertension |
| 120901804 | 12090180 | 3 | Blood cholesterol increased |
| 120901804 | 12090180 | 4 | Hypertension |
| 120901804 | 12090180 | 5 | Product used for unknown indication |
| 120901804 | 12090180 | 6 | Depression |
| 120901804 | 12090180 | 7 | Anxiety |
| 120901804 | 12090180 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120901804 | 12090180 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120901804 | 12090180 | Diarrhoea haemorrhagic | |
| 120901804 | 12090180 | Diverticulum | |
| 120901804 | 12090180 | Malabsorption | |
| 120901804 | 12090180 | Umbilical hernia |
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 |
|---|---|---|---|---|---|---|
| 120901804 | 12090180 | 1 | 20080311 | 20090221 | 0 | |
| 120901804 | 12090180 | 2 | 20090221 | 20110111 | 0 | |
| 120901804 | 12090180 | 3 | 200801 | 200803 | 0 | |
| 120901804 | 12090180 | 4 | 200712 | 0 | ||
| 120901804 | 12090180 | 6 | 200803 | 201502 | 0 |