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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121958453 | 12195845 | 3 | F | 20160720 | 20160321 | 20160804 | PER | US-PFIZER INC-2016112010 | PFIZER | 43.00 | YR | F | Y | 0.00000 | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121958453 | 12195845 | 1 | PS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | UNK | 19999 | |||||||||||
| 121958453 | 12195845 | 2 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | 19999 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121958453 | 12195845 | 1 | Mastectomy |
| 121958453 | 12195845 | 2 | Neuralgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121958453 | 12195845 | Drug hypersensitivity | |
| 121958453 | 12195845 | Somnolence | |
| 121958453 | 12195845 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 121958453 | 12195845 | 1 | 19911121 | 19911126 | 0 |