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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126555032 | 12655503 | 2 | F | 20160213 | 20160816 | 20160816 | PER | US-PFIZER INC-2016010116 | PFIZER | 0.00 | F | Y | 56.50000 | KG | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126555032 | 12655503 | 1 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | UNK | U | 0 | ||||||||||
| 126555032 | 12655503 | 2 | PS | AMPICILLIN SODIUM. | AMPICILLIN SODIUM | 1 | UNK | U | 202864 | ||||||||||
| 126555032 | 12655503 | 3 | SS | KETAMINE | KETAMINE | 1 | UNK | U | 0 | ||||||||||
| 126555032 | 12655503 | 4 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 126555032 | 12655503 | 5 | SS | PEGASPARGASE | PEGASPARGASE | 1 | UNK | U | 0 | ||||||||||
| 126555032 | 12655503 | 6 | SS | MICAFUNGIN | MICAFUNGIN | 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 |
|---|---|---|---|
| 126555032 | 12655503 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |