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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126938671 | 12693867 | 1 | I | 20160822 | 20160829 | 20160829 | PER | US-PFIZER INC-2016399537 | PFIZER | 0.00 | F | Y | 0.00000 | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126938671 | 12693867 | 1 | PS | CELEBREX | CELECOXIB | 1 | UNK | U | 20998 | CAPSULE, HARD | |||||||||
126938671 | 12693867 | 2 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | UNK | U | 21260 | PROLONGED-RELEASE CAPSULE | |||||||||
126938671 | 12693867 | 3 | SS | CEFOXITIN SODIUM | CEFOXITIN SODIUM | 1 | UNK | U | 65312 | ||||||||||
126938671 | 12693867 | 4 | SS | NORFLOXACIN | NORFLOXACIN | 1 | UNK | U | 0 | ||||||||||
126938671 | 12693867 | 5 | SS | ALBUTEROL. | ALBUTEROL | 1 | UNK | U | 0 | ||||||||||
126938671 | 12693867 | 6 | SS | CAFFEINE. | CAFFEINE | 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 |
---|---|---|---|
126938671 | 12693867 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |