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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
89021202 | 8902120 | 2 | F | 2016 | 20160811 | 20121112 | 20160928 | PER | US-ASTRAZENECA-2011SE52894 | ASTRAZENECA | 76.00 | YR | F | Y | 0.00000 | 20160928 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
89021202 | 8902120 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 2 PUFFS TWICE DAILY | 21929 | BID | |||||||||
89021202 | 8902120 | 2 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 | |||||||||||
89021202 | 8902120 | 3 | C | INCRUSE ELLIPTA | UMECLIDINIUM BROMIDE | 1 | 0 | ||||||||||||
89021202 | 8902120 | 4 | C | PRAVASTATIN. | PRAVASTATIN | 1 | 0 | ||||||||||||
89021202 | 8902120 | 5 | C | CARVEDILOL. | CARVEDILOL | 1 | 0 | ||||||||||||
89021202 | 8902120 | 6 | C | VALSARTAN. | VALSARTAN | 1 | 0 | ||||||||||||
89021202 | 8902120 | 7 | C | FUROSIMIDE | FUROSEMIDE | 1 | 0 | ||||||||||||
89021202 | 8902120 | 8 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
89021202 | 8902120 | 9 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
89021202 | 8902120 | 1 | Chronic obstructive pulmonary disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
89021202 | 8902120 | Device failure | |
89021202 | 8902120 | Intentional device misuse | |
89021202 | 8902120 | Lung disorder | |
89021202 | 8902120 | Pulmonary function test decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |