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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126359172 | 12635917 | 2 | F | 20160805 | 20160809 | 20160812 | PER | US-PFIZER INC-2016374319 | PFIZER | 0.00 | F | Y | 0.00000 | 20160812 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126359172 | 12635917 | 1 | PS | DILANTIN | PHENYTOIN | 1 | UNK | U | 10151 | ||||||||||
126359172 | 12635917 | 2 | SS | MOTRIN | IBUPROFEN | 1 | UNK | U | 18989 | FILM-COATED TABLET | |||||||||
126359172 | 12635917 | 3 | SS | PHENYTOIN SODIUM. | PHENYTOIN SODIUM | 1 | UNK | U | 10151 | ||||||||||
126359172 | 12635917 | 4 | SS | TORADOL | KETOROLAC TROMETHAMINE | 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 |
---|---|---|---|
126359172 | 12635917 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |