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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127081412 | 12708141 | 2 | F | 2014 | 20160831 | 20160901 | 20160924 | PER | US-ASTRAZENECA-2016SE80056 | ASTRAZENECA | 70.00 | YR | F | Y | 66.70000 | KG | 20160924 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127081412 | 12708141 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5MCG, 2 PUFFS TWICE A DAY | 3001189C00 | 21929 | |||||||||
127081412 | 12708141 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5MCG, 2 PUFFS TWICE A DAY | 3001189C00 | 21929 | |||||||||
127081412 | 12708141 | 3 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | 0 | 10 | MG | TABLET | QD | |||||||
127081412 | 12708141 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | Oral | 0 | 6.5 | MG | BID | ||||||||
127081412 | 12708141 | 5 | C | CALCIUM WITH VITAMIN D | CALCIUMVITAMIN D | 1 | Oral | 0 | 600 | MG | BID | ||||||||
127081412 | 12708141 | 6 | C | FLAXSEED | FLAX SEED | 1 | 0 | 100 | MG | QD | |||||||||
127081412 | 12708141 | 7 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 0 | 10 | MG | QD | ||||||||
127081412 | 12708141 | 8 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | Oral | 0 | |||||||||||
127081412 | 12708141 | 9 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 0 | 81 | UG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127081412 | 12708141 | 1 | Bronchitis chronic |
127081412 | 12708141 | 2 | Bronchitis chronic |
127081412 | 12708141 | 5 | Osteopenia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127081412 | 12708141 | Cough | |
127081412 | 12708141 | Device issue | |
127081412 | 12708141 | Intentional device misuse | |
127081412 | 12708141 | Pulmonary function test decreased | |
127081412 | 12708141 | Weight decreased |
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 |
---|---|---|---|---|---|---|
127081412 | 12708141 | 1 | 2014 | 0 | ||
127081412 | 12708141 | 2 | 201606 | 0 | ||
127081412 | 12708141 | 7 | 2012 | 0 | ||
127081412 | 12708141 | 8 | 2011 | 0 | ||
127081412 | 12708141 | 9 | 2012 | 0 |