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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125528551 | 12552855 | 1 | I | 20160628 | 20160704 | 20160713 | 20160713 | EXP | NL-LRB-221542 | PHHY2016NL092889 | SANDOZ | 2.01 | YR | M | Y | 0.00000 | 20160713 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125528551 | 12552855 | 1 | PS | SALBUTAMOL SANDOZ | ALBUTEROL | 1 | Respiratory (inhalation) | EXTRA INFO: 2 PUFF A 20 MIN DRIEMAAL, DAARNA 2 PUFF A 1 UUR 8 MAAL | Y | 72151 | SOLUTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125528551 | 12552855 | 1 | Dyspnoea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125528551 | 12552855 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125528551 | 12552855 | Dyspnoea | |
| 125528551 | 12552855 | Product quality issue | |
| 125528551 | 12552855 | 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 |
|---|---|---|---|---|---|---|
| 125528551 | 12552855 | 1 | 20160628 | 20160628 | 0 |