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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81856752 | 8185675 | 2 | F | 201609 | 20160909 | 20111018 | 20160930 | EXP | US-ASTRAZENECA-2011SE26803 | ASTRAZENECA | 78.00 | YR | F | Y | 79.40000 | KG | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81856752 | 8185675 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160 AND 4.5 TWO PUFFS TWICE A DAY | 21929 | BID | |||||||||
| 81856752 | 8185675 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160 AND 4.5 TWO PUFFS TWICE A DAY | 21929 | BID | |||||||||
| 81856752 | 8185675 | 3 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 0 | 10 | MG | TABLET | QD | |||||||
| 81856752 | 8185675 | 4 | SS | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 0 | 40 | MG | QD | ||||||||
| 81856752 | 8185675 | 5 | C | ALLERGY PILL | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
| 81856752 | 8185675 | 6 | C | BLOOD PRESSURE PILL | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
| 81856752 | 8185675 | 7 | C | WATER PILL | UNSPECIFIED INGREDIENT | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 81856752 | 8185675 | 1 | Emphysema |
| 81856752 | 8185675 | 2 | Chronic obstructive pulmonary disease |
| 81856752 | 8185675 | 3 | Blood cholesterol increased |
| 81856752 | 8185675 | 4 | Dyspepsia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 81856752 | 8185675 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 81856752 | 8185675 | Asthenia | |
| 81856752 | 8185675 | Blood cholesterol increased | |
| 81856752 | 8185675 | Drug dose omission | |
| 81856752 | 8185675 | Dyspepsia | |
| 81856752 | 8185675 | Emphysema | |
| 81856752 | 8185675 | Fall | |
| 81856752 | 8185675 | Fatigue | |
| 81856752 | 8185675 | Fluid retention | |
| 81856752 | 8185675 | Influenza | |
| 81856752 | 8185675 | Nasopharyngitis | |
| 81856752 | 8185675 | Pulmonary thrombosis |
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 |
|---|---|---|---|---|---|---|
| 81856752 | 8185675 | 1 | 2013 | 0 | ||
| 81856752 | 8185675 | 2 | 2013 | 0 | ||
| 81856752 | 8185675 | 3 | 2013 | 0 |