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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127687751 | 12768775 | 1 | I | 20160704 | 20160913 | 20160921 | 20160921 | EXP | US-ASTRAZENECA-2016SE97882 | ASTRAZENECA | 0.00 | E | F | Y | 108.80000 | KG | 20160921 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127687751 | 12768775 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, TWO INHALATIONS TWO TIMES DAILY | 21929 | BID | |||||||||
127687751 | 12768775 | 2 | SS | EYLEA | AFLIBERCEPT | 1 | Intraocular | 0 | 2 | MG | INJECTION | /month | |||||||
127687751 | 12768775 | 3 | SS | EYLEA | AFLIBERCEPT | 1 | Intraocular | 0 | 2 | MG | INJECTION | /month | |||||||
127687751 | 12768775 | 4 | SS | EYLEA | AFLIBERCEPT | 1 | Intraocular | 0 | 2 | MG | INJECTION | /month | |||||||
127687751 | 12768775 | 5 | SS | GABAPENTIN. | GABAPENTIN | 1 | Unknown | Y | U | 0 | |||||||||
127687751 | 12768775 | 6 | SS | GABAPENTIN. | GABAPENTIN | 1 | Unknown | Y | U | 0 | |||||||||
127687751 | 12768775 | 7 | SS | AZELASTINE HCL | AZELASTINE HYDROCHLORIDE | 1 | Nasal | 0 | |||||||||||
127687751 | 12768775 | 8 | SS | FLONASE | FLUTICASONE PROPIONATE | 1 | Nasal | 0 | |||||||||||
127687751 | 12768775 | 9 | SS | MONTELUKAST | MONTELUKAST SODIUM | 1 | Unknown | 0 | 10 | MG | QD | ||||||||
127687751 | 12768775 | 10 | SS | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Unknown | 0 | |||||||||||
127687751 | 12768775 | 11 | SS | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | 0 | 10 | MG | QD | ||||||||
127687751 | 12768775 | 12 | SS | ALBUTEROL. | ALBUTEROL | 1 | Unknown | 180.0UG AS REQUIRED | 0 | 180 | UG | ||||||||
127687751 | 12768775 | 13 | C | LOSARTAN/HCTZ | HYDROCHLOROTHIAZIDELOSARTAN | 1 | 0 | ||||||||||||
127687751 | 12768775 | 14 | C | ZETIA | EZETIMIBE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127687751 | 12768775 | 2 | Macular degeneration |
127687751 | 12768775 | 3 | Macular degeneration |
127687751 | 12768775 | 4 | Macular degeneration |
127687751 | 12768775 | 5 | Spinal column stenosis |
127687751 | 12768775 | 6 | Spinal column stenosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127687751 | 12768775 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127687751 | 12768775 | Asthma | |
127687751 | 12768775 | Eosinophil count increased | |
127687751 | 12768775 | Pulmonary function test decreased | |
127687751 | 12768775 | Transient ischaemic attack |
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 |
---|---|---|---|---|---|---|
127687751 | 12768775 | 2 | 20160524 | 0 | ||
127687751 | 12768775 | 3 | 20160621 | 0 | ||
127687751 | 12768775 | 4 | 20160719 | 0 | ||
127687751 | 12768775 | 5 | 201601 | 201602 | 0 | |
127687751 | 12768775 | 6 | 20160703 | 201607 | 0 |