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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125401591 | 12540159 | 1 | I | 2016 | 20160629 | 20160708 | 20160708 | EXP | FR-PFIZER INC-2016323869 | PFIZER | 73.00 | YR | F | Y | 0.00000 | 20160708 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125401591 | 12540159 | 1 | PS | ALDACTONE | SPIRONOLACTONE | 1 | Oral | 25 MG, DAILY | Y | 12151 | 25 | MG | FILM-COATED TABLET | ||||||
| 125401591 | 12540159 | 2 | SS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 50 MG, 2X/DAY | Y | 0 | 50 | MG | COATED TABLET | BID | |||||
| 125401591 | 12540159 | 3 | SS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 150 MG, UNK | Y | 0 | 150 | MG | COATED TABLET | ||||||
| 125401591 | 12540159 | 4 | SS | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | Oral | 60 MG, DAILY | Y | 0 | 60 | MG | |||||||
| 125401591 | 12540159 | 5 | SS | LASILIX /00032601/ | FUROSEMIDE | 1 | Oral | 20 MG, DAILY | Y | 0 | 20 | MG | TABLET | ||||||
| 125401591 | 12540159 | 6 | SS | TEMESTA /00273201/ | LORAZEPAM | 1 | Oral | 1 MG, 5 TIMES DAILY | Y | 0 | 5 | MG | TABLET | ||||||
| 125401591 | 12540159 | 7 | C | ZOPICLONE | ZOPICLONE | 1 | 0 | ||||||||||||
| 125401591 | 12540159 | 8 | C | TAHOR | ATORVASTATIN CALCIUM | 1 | 0 | ||||||||||||
| 125401591 | 12540159 | 9 | C | SOTALEX | SOTALOL | 1 | 160 MG, UNK | 0 | 160 | MG | |||||||||
| 125401591 | 12540159 | 10 | C | DIFFU K | POTASSIUM CHLORIDE | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125401591 | 12540159 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125401591 | 12540159 | Hyponatraemia | |
| 125401591 | 12540159 | Insomnia | |
| 125401591 | 12540159 | Status epilepticus | |
| 125401591 | 12540159 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 125401591 | 12540159 | 1 | 20160607 | 0 | ||
| 125401591 | 12540159 | 3 | 20160607 | 0 | ||
| 125401591 | 12540159 | 4 | 20160607 | 0 | ||
| 125401591 | 12540159 | 5 | 20160607 | 0 | ||
| 125401591 | 12540159 | 6 | 20160607 | 0 |