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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105968675 | 10596867 | 5 | F | 20160713 | 20141120 | 20160719 | EXP | US-ASTRAZENECA-2014SE86318 | ASTRAZENECA | 0.00 | M | Y | 85.30000 | KG | 20160719 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105968675 | 10596867 | 1 | PS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | Y | U | 202450 | INHALATION POWDER | ||||||||
| 105968675 | 10596867 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80/4.5 MCG, 2 PUFFS TWO TIMES A DAY | 0 | BID | |||||||||
| 105968675 | 10596867 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80/4.5 MCG, 2 PUFFS TWO TIMES A DAY | 0 | BID | |||||||||
| 105968675 | 10596867 | 4 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 1 PUFF TWO TIMES A DAY (AGAINST PRESCRIPTION, AS REQUIRED) | 0 | BID | |||||||||
| 105968675 | 10596867 | 5 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 1 PUFF TWO TIMES A DAY (AGAINST PRESCRIPTION, AS REQUIRED) | 0 | BID | |||||||||
| 105968675 | 10596867 | 6 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS EVERY 12 HOURS | 0 | Q12H | |||||||||
| 105968675 | 10596867 | 7 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS EVERY 12 HOURS | 0 | Q12H | |||||||||
| 105968675 | 10596867 | 8 | SS | DALIRESP | ROFLUMILAST | 1 | Oral | 0 | 500 | UG | TABLET | QD | |||||||
| 105968675 | 10596867 | 9 | C | OTC (OVER THE COUNTER) GENERIC ANTIHISTAMINE | 2 | Oral | 0 | 1 | DF | TABLET | BID | ||||||||
| 105968675 | 10596867 | 10 | C | GENERIC OTC MUCINEX | 2 | Oral | 0 | 400 | MG | BID | |||||||||
| 105968675 | 10596867 | 11 | C | GENERIC TAGAMET | 2 | Oral | 0 | 1 | DF | TABLET | QD | ||||||||
| 105968675 | 10596867 | 12 | C | GENERIC TAGAMET | 2 | Oral | 0 | 1 | DF | TABLET | QD | ||||||||
| 105968675 | 10596867 | 13 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 0 | |||||||||||
| 105968675 | 10596867 | 14 | C | BLOOD PRESSURE MEDICATION | UNSPECIFIED INGREDIENT | 1 | 0 | 90 | MG | QD | |||||||||
| 105968675 | 10596867 | 15 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 | ||||||||||||
| 105968675 | 10596867 | 16 | C | ANTIHISTAMINE | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
| 105968675 | 10596867 | 17 | C | VITAMINS | VITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105968675 | 10596867 | 1 | Chronic obstructive pulmonary disease |
| 105968675 | 10596867 | 2 | Chronic obstructive pulmonary disease |
| 105968675 | 10596867 | 3 | Bronchitis chronic |
| 105968675 | 10596867 | 4 | Chronic obstructive pulmonary disease |
| 105968675 | 10596867 | 5 | Bronchitis chronic |
| 105968675 | 10596867 | 6 | Chronic obstructive pulmonary disease |
| 105968675 | 10596867 | 7 | Bronchitis chronic |
| 105968675 | 10596867 | 8 | Chronic obstructive pulmonary disease |
| 105968675 | 10596867 | 10 | Nasal congestion |
| 105968675 | 10596867 | 11 | Ulcer |
| 105968675 | 10596867 | 12 | Ulcer |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 105968675 | 10596867 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105968675 | 10596867 | Abdominal discomfort | |
| 105968675 | 10596867 | Cataract | |
| 105968675 | 10596867 | Diarrhoea | |
| 105968675 | 10596867 | Dysphagia | |
| 105968675 | 10596867 | Dyspnoea | |
| 105968675 | 10596867 | Intentional product misuse | |
| 105968675 | 10596867 | Intentional product use issue | |
| 105968675 | 10596867 | Local swelling | |
| 105968675 | 10596867 | Pharyngeal oedema | |
| 105968675 | 10596867 | Productive cough | |
| 105968675 | 10596867 | Pulmonary function test decreased | |
| 105968675 | 10596867 | Throat irritation | |
| 105968675 | 10596867 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 105968675 | 10596867 | 2 | 2009 | 0 | ||
| 105968675 | 10596867 | 3 | 2009 | 0 | ||
| 105968675 | 10596867 | 4 | 201501 | 0 | ||
| 105968675 | 10596867 | 5 | 201501 | 0 | ||
| 105968675 | 10596867 | 8 | 20160603 | 0 | ||
| 105968675 | 10596867 | 11 | 1984 | 0 | ||
| 105968675 | 10596867 | 12 | 1984 | 0 |