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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126348991 | 12634899 | 1 | I | 20160720 | 20160809 | 20160809 | PER | US-PFIZER INC-2016355314 | PFIZER | 46.00 | YR | F | Y | 0.00000 | 20160809 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126348991 | 12634899 | 1 | PS | DILANTIN | PHENYTOIN | 1 | U | 10151 | |||||||||||
| 126348991 | 12634899 | 2 | SS | ASA | ASPIRIN | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 3 | SS | KEPPRA | LEVETIRACETAM | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 4 | SS | LAMICTAL | LAMOTRIGINE | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 5 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 6 | SS | MOTRIN | IBUPROFEN | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 7 | SS | PHENERGAN | PROMETHAZINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 8 | SS | TEGRETOL | CARBAMAZEPINE | 1 | U | 0 | |||||||||||
| 126348991 | 12634899 | 9 | SS | TORADOL | KETOROLAC TROMETHAMINE | 1 | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126348991 | 12634899 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |