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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126012681 | 12601268 | 1 | I | 2011 | 20160720 | 20160728 | 20160728 | EXP | US-ASTRAZENECA-2016SE80023 | ASTRAZENECA | 61.00 | YR | F | Y | 95.70000 | KG | 20160728 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126012681 | 12601268 | 1 | PS | RHINOCORT AQUA | BUDESONIDE | 1 | Nasal | TWO SPRAYS EACH NOSTRIL DAILY AS NEEDED | 20746 | NASAL SPRAY | |||||||||
| 126012681 | 12601268 | 2 | SS | RHINOCORT AQUA | BUDESONIDE | 1 | Nasal | TWO SPRAYS EACH NOSTRIL DAILY AS NEEDED | 20746 | NASAL SPRAY | |||||||||
| 126012681 | 12601268 | 3 | SS | RHINOCORT AQUA | BUDESONIDE | 1 | Nasal | TWO SPRAYS EACH NOSTRIL DAILY AS NEEDED | 20746 | NASAL SPRAY | |||||||||
| 126012681 | 12601268 | 4 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | TOOK A TOTAL OF 4 PUFFS | Y | U | 0 | ||||||||
| 126012681 | 12601268 | 5 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126012681 | 12601268 | 1 | Pulmonary congestion |
| 126012681 | 12601268 | 2 | Multiple allergies |
| 126012681 | 12601268 | 3 | Sinusitis |
| 126012681 | 12601268 | 4 | Lung disorder |
| 126012681 | 12601268 | 5 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126012681 | 12601268 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126012681 | 12601268 | Drug hypersensitivity | |
| 126012681 | 12601268 | Erythema | |
| 126012681 | 12601268 | Off label use | |
| 126012681 | 12601268 | Pneumonia | |
| 126012681 | 12601268 | Product use issue | |
| 126012681 | 12601268 | Pruritus | |
| 126012681 | 12601268 | Urticaria | |
| 126012681 | 12601268 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 126012681 | 12601268 | 1 | 2010 | 0 | ||
| 126012681 | 12601268 | 2 | 2010 | 0 | ||
| 126012681 | 12601268 | 3 | 2010 | 0 | ||
| 126012681 | 12601268 | 4 | 2011 | 0 |