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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127997881 | 12799788 | 1 | I | 20160225 | 20160926 | 20160930 | 20160930 | PER | US-PFIZER INC-2016454211 | PFIZER | 86.00 | YR | Y | 0.00000 | 20160930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127997881 | 12799788 | 1 | PS | CELECOXIB. | CELECOXIB | 1 | UNK | U | 20998 | ||||||||||
127997881 | 12799788 | 2 | SS | ESOMEPRAZOLE MAGNESIUM. | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | U | 0 | ||||||||||
127997881 | 12799788 | 3 | SS | LEVOFLOXACIN. | LEVOFLOXACIN | 1 | UNK | U | 78577 | ||||||||||
127997881 | 12799788 | 4 | SS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | UNK | U | 77245 | ||||||||||
127997881 | 12799788 | 5 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
127997881 | 12799788 | 6 | SS | OLMESARTAN | OLMESARTAN | 1 | UNK | U | 0 | ||||||||||
127997881 | 12799788 | 7 | SS | RABEPRAZOLE SODIUM. | RABEPRAZOLE SODIUM | 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 |
---|---|---|---|
127997881 | 12799788 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |