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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127438002 | 12743800 | 2 | F | 20160912 | 20160914 | 20160920 | EXP | PHHY2016PL123405 | SANDOZ | PEDIATRIA PO DYPLOMIE NR 4/2016 | 4.00 | YR | F | Y | 0.00000 | 20160921 | OT | PL | PL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127438002 | 12743800 | 1 | PS | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Unknown | U | 65136 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127438002 | 12743800 | 1 | Bronchitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127438002 | 12743800 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127438002 | 12743800 | Blister | |
| 127438002 | 12743800 | Erythema | |
| 127438002 | 12743800 | Nasal mucosal disorder | |
| 127438002 | 12743800 | Oedema | |
| 127438002 | 12743800 | Pneumonia | |
| 127438002 | 12743800 | Pruritus | |
| 127438002 | 12743800 | Rales | |
| 127438002 | 12743800 | Urticaria |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |