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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127173042 | 12717304 | 2 | F | 2016 | 20160923 | 20160906 | 20160928 | EXP | CN-GLAXOSMITHKLINE-CN2016GSK125867 | GLAXOSMITHKLINE | 59.00 | YR | F | Y | 0.00000 | 20160928 | CN | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127173042 | 12717304 | 1 | PS | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | UNK | 21077 | 1 | DF | INHALATION POWDER | |||||||
127173042 | 12717304 | 2 | SS | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 2 PUFF(S), UNK | 21077 | 2 | DF | INHALATION POWDER | ||||||||
127173042 | 12717304 | 3 | SS | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | RD9Y | 21077 | INHALATION POWDER | |||||||||
127173042 | 12717304 | 4 | SS | Salbutamol sulphate | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | UNK | Y | 0 | INHALATION POWDER |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127173042 | 12717304 | 1 | Asthma |
127173042 | 12717304 | 4 | Asthma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127173042 | 12717304 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127173042 | 12717304 | Abdominal discomfort | |
127173042 | 12717304 | Asthma | |
127173042 | 12717304 | Bronchospasm | |
127173042 | 12717304 | Decreased appetite | |
127173042 | 12717304 | Drug ineffective | |
127173042 | 12717304 | Intentional product misuse | |
127173042 | 12717304 | Product quality issue |
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 |
---|---|---|---|---|---|---|
127173042 | 12717304 | 1 | 201602 | 0 |