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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127390341 | 12739034 | 1 | I | 201608 | 20160907 | 20160913 | 20160913 | EXP | FR-PFIZER INC-2016421720 | PFIZER | 30.00 | YR | M | Y | 0.00000 | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127390341 | 12739034 | 1 | PS | ALDACTONE | SPIRONOLACTONE | 1 | Oral | Y | 12151 | FILM-COATED TABLET | |||||||||
| 127390341 | 12739034 | 2 | SS | TESTOSTERONE PROPIONATE. | TESTOSTERONE PROPIONATE | 1 | Intramuscular | 1 MG, DAILY | Y | 0 | 1 | MG | |||||||
| 127390341 | 12739034 | 3 | SS | ARIMIDEX | ANASTROZOLE | 1 | Oral | Y | 0 | ||||||||||
| 127390341 | 12739034 | 4 | SS | CLENBUTEROL | CLENBUTEROL | 1 | Y | 0 | |||||||||||
| 127390341 | 12739034 | 5 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 500 UG, DAILY | 0 | 500 | UG | |||||||||
| 127390341 | 12739034 | 6 | C | VENTOLINE /00139501/ | ALBUTEROL | 1 | UNK, AS NEEDED | 0 | |||||||||||
| 127390341 | 12739034 | 7 | C | WINSTROL | STANOZOLOL | 1 | Oral | 50 MG, DAILY | 0 | 50 | MG | ||||||||
| 127390341 | 12739034 | 8 | C | SOMATOTROPIN (HUMAN) | 2 | Subcutaneous | 6.5 MG, DAILY | 0 | 6.5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127390341 | 12739034 | 5 | Asthma |
| 127390341 | 12739034 | 6 | Asthma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127390341 | 12739034 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127390341 | 12739034 | Pancreatitis acute | |
| 127390341 | 12739034 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |