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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124971722 | 12497172 | 2 | F | 2014 | 20160722 | 20160624 | 20160729 | EXP | GB-ASTRAZENECA-2016SE68140 | ASTRAZENECA | 53.00 | YR | F | Y | 68.00000 | KG | 20160729 | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124971722 | 12497172 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 200/6 UG WITH UNKNOWN FREQUENCY UNKNOWN | 21929 | INHALATION POWDER | |||||||||
124971722 | 12497172 | 2 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | AS REQUIRED | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124971722 | 12497172 | 1 | Asthma |
124971722 | 12497172 | 2 | Asthma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124971722 | 12497172 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124971722 | 12497172 | Asthma | |
124971722 | 12497172 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |