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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127674341 | 12767434 | 1 | I | 20160824 | 20160909 | 20160921 | 20160921 | EXP | GB-MHRA-EYC 00144805 | GB-TEVA-693247ACC | TEVA | 32.00 | YR | M | Y | 80.00000 | KG | 20160921 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127674341 | 12767434 | 1 | PS | ERYTHROMYCIN. | ERYTHROMYCIN | 1 | Oral | 2000 MILLIGRAM DAILY; | 12000 | MG | Y | U | 62999 | 500 | MG | QID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127674341 | 12767434 | 1 | Ear infection bacterial |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127674341 | 12767434 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127674341 | 12767434 | Acute kidney injury | |
| 127674341 | 12767434 | Nausea | |
| 127674341 | 12767434 | Pharyngeal oedema | |
| 127674341 | 12767434 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 127674341 | 12767434 | 1 | 20160818 | 20160824 | 0 |