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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 93061587 | 9306158 | 7 | F | 2009 | 20160809 | 20130523 | 20160815 | PER | US-PFIZER INC-2013156629 | PFIZER | 72.00 | YR | F | Y | 96.50000 | KG | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 93061587 | 9306158 | 1 | PS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | UNK | 19999 | |||||||||||
| 93061587 | 9306158 | 2 | SS | DAYPRO | OXAPROZIN | 1 | UNK | 18841 | TABLET | ||||||||||
| 93061587 | 9306158 | 3 | SS | TEGRETOL | CARBAMAZEPINE | 1 | UNK | U | 0 | ||||||||||
| 93061587 | 9306158 | 4 | SS | TRAMADOL. | TRAMADOL | 1 | UNK | U | 0 | ||||||||||
| 93061587 | 9306158 | 5 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 93061587 | 9306158 | 2 | Fibromyalgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 93061587 | 9306158 | Drug hypersensitivity |
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 |
|---|---|---|---|---|---|---|
| 93061587 | 9306158 | 2 | 199803 | 199803 | 0 |