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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
103712072 | 10371207 | 2 | F | 20151229 | 20140808 | 20151231 | PER | US-PFIZER INC-2014219843 | PFIZER | 51.00 | YR | M | Y | 0.00000 | 20151231 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
103712072 | 10371207 | 1 | SS | RIFAMPICIN | RIFAMPIN | 1 | UNK | 0 | |||||||||||
103712072 | 10371207 | 2 | PS | DOXYCYCLINE CALCIUM | DOXYCYCLINE CALCIUM | 1 | UNK | 50480 | SYRUP | ||||||||||
103712072 | 10371207 | 3 | SS | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | UNK | 0 | |||||||||||
103712072 | 10371207 | 4 | SS | IMURAN | AZATHIOPRINE | 1 | UNK | 0 | |||||||||||
103712072 | 10371207 | 5 | SS | ETHAMBUTOL | ETHAMBUTOL HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
103712072 | 10371207 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |