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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127829311 | 12782931 | 1 | I | 20160922 | 20160927 | 20160927 | PER | US-PFIZER INC-2016448240 | PFIZER | 76.00 | YR | F | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127829311 | 12782931 | 1 | PS | CORTISONE | CORTISONEHYDROCORTISONE | 1 | UNK | U | 8126 | TABLET | |||||||||
| 127829311 | 12782931 | 2 | SS | MOTRIN | IBUPROFEN | 1 | UNK | U | 0 | ||||||||||
| 127829311 | 12782931 | 3 | SS | CIPRO | CIPROFLOXACIN HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 127829311 | 12782931 | 4 | SS | CLARITIN | LORATADINE | 1 | UNK | U | 0 | ||||||||||
| 127829311 | 12782931 | 5 | SS | DARVOCET-N 100 | ACETAMINOPHENPROPOXYPHENE NAPSYLATE | 1 | UNK | U | 0 | ||||||||||
| 127829311 | 12782931 | 6 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | UNK | U | 0 | ||||||||||
| 127829311 | 12782931 | 7 | SS | ULTRAM | TRAMADOL 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 |
|---|---|---|---|
| 127829311 | 12782931 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |