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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126228181 | 12622818 | 1 | I | 20150202 | 20160726 | 20160804 | 20160804 | EXP | CH-SM-2016-06146 | CH-PFIZER INC-2016363864 | PFIZER | 86.00 | YR | F | Y | 0.00000 | 20160804 | MD | CH | CH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126228181 | 12622818 | 1 | PS | ALDACTONE | SPIRONOLACTONE | 1 | Oral | 25 MG, 2X/DAY | 12151 | 25 | MG | FILM-COATED TABLET | BID | ||||||
| 126228181 | 12622818 | 2 | SS | ASPIRIN CARDIO | ASPIRIN | 1 | Oral | 100 MG, 1X/DAY (1-0-0-0) | 0 | 100 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 3 | SS | PREDNISON | PREDNISONE | 1 | Oral | 10 MG, 1X/DAY (0.5 (20 MG)-0-0-0) | 0 | 10 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 4 | SS | KCL-RETARD | POTASSIUM CHLORIDE | 1 | Oral | 10 MMOL, 1X/DAY | 0 | 10 | MMOL | COATED TABLET | QD | ||||||
| 126228181 | 12622818 | 5 | C | MST CONTINUS | MORPHINE SULFATE | 1 | Oral | 10 MG, 2X/DAY (1-0-1-0) | 0 | 10 | MG | TABLET | BID | ||||||
| 126228181 | 12622818 | 6 | C | CALCIMAGON D3 | CALCIUMCHOLECALCIFEROL | 1 | Oral | 1 DF, 2X/DAY (1-0-1-0) | 0 | 1 | DF | LOZENGE | BID | ||||||
| 126228181 | 12622818 | 7 | C | MOTILIUM | DOMPERIDONE | 1 | Oral | 10 MG, 3X/DAY (1-1-1-0) | 0 | 10 | MG | TABLET | TID | ||||||
| 126228181 | 12622818 | 8 | C | METOLAZON | METOLAZONE | 1 | Oral | 5 MG, 1X/DAY (1-0-0-0) | 0 | 5 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 9 | C | AMLODIPIN /00972401/ | AMLODIPINE BESYLATE | 1 | Oral | 10 MG, 1X/DAY (0-1-0-0) | 0 | 10 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 10 | C | TEMESTA /00273201/ | LORAZEPAM | 1 | 1 MG, 1X/DAY (0-0-0-1) | 0 | 1 | MG | TABLET | QD | |||||||
| 126228181 | 12622818 | 11 | C | TARDYFERON | FERROUS SULFATE | 1 | Oral | 1 DF, 2X/DAY (1-0-1-0) | 0 | 1 | DF | COATED TABLET | BID | ||||||
| 126228181 | 12622818 | 12 | C | VITALUX /01586901/ | 2 | 1 DF, 1X/DAY (0-1-0-0) | 0 | 1 | DF | CAPSULE | QD | ||||||||
| 126228181 | 12622818 | 13 | C | TORASEMID SANDOZ | TORSEMIDE | 1 | Oral | 100 MG, 2X/DAY (0.5 (200 MG)-0.5-0-0) | 0 | 100 | MG | TABLET | BID | ||||||
| 126228181 | 12622818 | 14 | C | PANTOZOL | PANTOPRAZOLE SODIUM | 1 | Oral | 40 MG, 1X/DAY (0-0-1-0) | 0 | 40 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 15 | C | RAMIPRIL. | RAMIPRIL | 1 | Oral | 2.5 MG, 2X/DAY (0.5(5 MG)-0-0.5-0) | 0 | 2.5 | MG | TABLET | BID | ||||||
| 126228181 | 12622818 | 16 | C | ELTROXIN | LEVOTHYROXINE | 1 | Oral | 0.05 MG, 1X/DAY (1-0-0-0) | 0 | .05 | MG | TABLET | QD | ||||||
| 126228181 | 12622818 | 17 | C | MORPHINI | MORPHINE HYDROCHLORIDE | 1 | Oral | 4 ML, 3X/DAY (6 H/12 H/18H) | 0 | 4 | ML | ORAL DROPS | TID | ||||||
| 126228181 | 12622818 | 18 | C | NOVALGIN | METAMIZOLE SODIUM | 1 | Oral | 20 GTT, 4X/DAY (1-1-1-1) | 0 | 20 | GTT | ORAL DROPS | QID | ||||||
| 126228181 | 12622818 | 19 | C | VI-DE 3 | CHOLECALCIFEROL | 1 | Oral | 20 GTT, 1X/DAY (1-0-0-0) | 0 | 20 | GTT | ORAL DROPS | QD | ||||||
| 126228181 | 12622818 | 20 | C | IMPORTAL | LACTITOL | 1 | Oral | 20 ML, 2X/DAY (1-0-1-0) | 0 | 20 | ML | BID | |||||||
| 126228181 | 12622818 | 21 | C | MOVICOL | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | Oral | 1 DF, ALTERNATE DAY (ODD NUMBERED DAYS) | 0 | 1 | DF | QOD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126228181 | 12622818 | DE |
| 126228181 | 12622818 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126228181 | 12622818 | Abdominal pain | |
| 126228181 | 12622818 | Death | |
| 126228181 | 12622818 | Haematemesis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |