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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127878931 | 12787893 | 1 | I | 20140808 | 20160928 | 20160928 | PER | US-PFIZER INC-2014223927 | PFIZER | 62.00 | YR | F | Y | 0.00000 | 20160928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127878931 | 12787893 | 1 | PS | MIDAZOLAM | MIDAZOLAMMIDAZOLAM HYDROCHLORIDE | 1 | UNK | U | 75293 | ||||||||||
| 127878931 | 12787893 | 2 | SS | OXYCODONE | OXYCODONE | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 3 | SS | MELOXICAM. | MELOXICAM | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 4 | SS | ATIVAN | LORAZEPAM | 1 | UNK | U | 74243 | ||||||||||
| 127878931 | 12787893 | 5 | SS | HYDROCORTISONE. | HYDROCORTISONE | 1 | UNK | U | 8697 | TABLET | |||||||||
| 127878931 | 12787893 | 6 | SS | ALEVE | NAPROXEN SODIUM | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 7 | SS | ASPIRIN. | ASPIRIN | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 8 | SS | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 9 | SS | HALDOL | HALOPERIDOL | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 10 | SS | HYDROCODONE W/ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | U | 0 | ||||||||||
| 127878931 | 12787893 | 11 | SS | DICYCLOMINE | DICYCLOMINE HYDROCHLORIDE | 1 | UNK | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127878931 | 12787893 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |