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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125965381 | 12596538 | 1 | I | 20160706 | 20160715 | 20160727 | 20160727 | EXP | GB-MHRA-TPP20695213C848998YC1467820160178 | GB-TEVA-678308ACC | TEVA | 35.00 | YR | F | Y | 73.00000 | KG | 20160727 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125965381 | 12596538 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | U | U | 61926 | ||||||||||
| 125965381 | 12596538 | 2 | C | AMITRIPTYLINE HYDROCHLORIDE. | AMITRIPTYLINE HYDROCHLORIDE | 1 | 1 DOSAGE FORMS DAILY; AT NIGHT | 202.958333 | DF | 0 | 1 | DF | QD | ||||||
| 125965381 | 12596538 | 3 | C | ERYTHROMYCIN. | ERYTHROMYCIN | 1 | 8 DOSAGE FORMS DAILY; | 8 | DF | 0 | 2 | DF | QID |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125965381 | 12596538 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125965381 | 12596538 | Rash | |
| 125965381 | 12596538 | Swelling |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125965381 | 12596538 | 1 | 20160706 | 0 | ||
| 125965381 | 12596538 | 2 | 20151216 | 0 | ||
| 125965381 | 12596538 | 3 | 20160706 | 0 |