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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127214271 | 12721427 | 1 | I | 20160318 | 20160831 | 20160907 | 20160907 | EXP | NL-LRB-224792 | PHHY2016NL119964 | SANDOZ | 9.35 | YR | F | Y | 23.00000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127214271 | 12721427 | 1 | PS | SALBUTAMOL SANDOZ | ALBUTEROL | 1 | Respiratory (inhalation) | WANNEER NODIG, MAX 8 X PER DAG | N | 72151 | 1 | DF | AEROSOL | ||||||
127214271 | 12721427 | 2 | C | FLIXOTIDE | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | 2 KEER PER DAG 2 STUK(S) | U | 0 | 2 | DF | AEROSOL | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127214271 | 12721427 | 1 | Asthma |
127214271 | 12721427 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127214271 | 12721427 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127214271 | 12721427 | Therapeutic response decreased | |
127214271 | 12721427 | Therapeutic response unexpected |
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 |
---|---|---|---|---|---|---|
127214271 | 12721427 | 1 | 2015 | 20160326 | 0 | |
127214271 | 12721427 | 2 | 20080101 | 0 |