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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 85320053 | 8532005 | 3 | F | 20120408 | 20160921 | 20120426 | 20160929 | EXP | US-ASTRAZENECA-2012SE25469 | ASTRAZENECA | 30702.00 | DY | M | Y | 99.80000 | KG | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 85320053 | 8532005 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160 MCG, ONE PUFF DAILY | 21929 | ||||||||||
| 85320053 | 8532005 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, TWO PUFFS A DAY | 21929 | ||||||||||
| 85320053 | 8532005 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, ONE PUFF A DAY | 21929 | ||||||||||
| 85320053 | 8532005 | 4 | C | VITAMINS NOS | VITAMINS | 1 | 0 | ||||||||||||
| 85320053 | 8532005 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 | ||||||||||||
| 85320053 | 8532005 | 6 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
| 85320053 | 8532005 | 7 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | 1 PUFF PER DAY | 0 | ||||||||||
| 85320053 | 8532005 | 8 | C | INJECTION INTO RIGHT EYE | 2 | 0 | |||||||||||||
| 85320053 | 8532005 | 9 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | ABOUT 1 WEEK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 85320053 | 8532005 | 1 | Chronic obstructive pulmonary disease |
| 85320053 | 8532005 | 2 | Chronic obstructive pulmonary disease |
| 85320053 | 8532005 | 3 | Chronic obstructive pulmonary disease |
| 85320053 | 8532005 | 5 | Blood cholesterol abnormal |
| 85320053 | 8532005 | 6 | Hypertension |
| 85320053 | 8532005 | 7 | Chronic obstructive pulmonary disease |
| 85320053 | 8532005 | 8 | Haemorrhage prophylaxis |
| 85320053 | 8532005 | 9 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 85320053 | 8532005 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 85320053 | 8532005 | Blood cholesterol increased | |
| 85320053 | 8532005 | Diarrhoea | |
| 85320053 | 8532005 | Flatulence | |
| 85320053 | 8532005 | Headache | |
| 85320053 | 8532005 | Herpes zoster | |
| 85320053 | 8532005 | Hypertension | |
| 85320053 | 8532005 | Intentional product misuse | |
| 85320053 | 8532005 | Nausea | |
| 85320053 | 8532005 | Off label use | |
| 85320053 | 8532005 | Vision blurred | |
| 85320053 | 8532005 | Visual acuity reduced |
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 |
|---|---|---|---|---|---|---|
| 85320053 | 8532005 | 1 | 201202 | 0 | ||
| 85320053 | 8532005 | 2 | 20160708 | 0 | ||
| 85320053 | 8532005 | 3 | 20160708 | 0 | ||
| 85320053 | 8532005 | 7 | 2006 | 0 |