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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127249561 | 12724956 | 1 | I | 20160717 | 20160831 | 20160908 | 20160908 | EXP | NL-LRB-224351 | PHHY2016NL119954 | SANDOZ | 11.00 | MON | F | Y | 9.00000 | KG | 20160908 | OT | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127249561 | 12724956 | 1 | PS | SALBUTAMOL SANDOZ | ALBUTEROL | 1 | Respiratory (inhalation) | 1 DF, TID | Y | RVG: 34432 | 72151 | 1 | DF | AEROSOL | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127249561 | 12724956 | 1 | Dyspnoea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127249561 | 12724956 | HO |
| 127249561 | 12724956 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127249561 | 12724956 | Dyspnoea | |
| 127249561 | 12724956 | Product quality issue | |
| 127249561 | 12724956 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 127249561 | 12724956 | 1 | 2016 | 0 |