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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125295293 | 12529529 | 3 | F | 2013 | 20160824 | 20160706 | 20160830 | EXP | US-ASTRAZENECA-2016SE71507 | ASTRAZENECA | 77.00 | YR | F | Y | 78.50000 | KG | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125295293 | 12529529 | 1 | PS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | U | U | 202450 | 400 | UG | INHALATION POWDER | BID | |||||
| 125295293 | 12529529 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS TWO TIMES DAILY | U | U | 0 | ||||||||
| 125295293 | 12529529 | 3 | C | OXYGEN. | OXYGEN | 1 | Respiratory (inhalation) | 0 | 1 | L | QD | ||||||||
| 125295293 | 12529529 | 4 | C | FLUCONAZOLE. | FLUCONAZOLE | 1 | Nasal | 0 | 1 | DF | NASAL SPRAY | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125295293 | 12529529 | 1 | Chronic obstructive pulmonary disease |
| 125295293 | 12529529 | 2 | Chronic obstructive pulmonary disease |
| 125295293 | 12529529 | 3 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125295293 | 12529529 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125295293 | 12529529 | Body height decreased | |
| 125295293 | 12529529 | Circumstance or information capable of leading to medication error | |
| 125295293 | 12529529 | Device malfunction | |
| 125295293 | 12529529 | Drug dose omission | |
| 125295293 | 12529529 | Intentional product misuse | |
| 125295293 | 12529529 | Pneumonia | |
| 125295293 | 12529529 | Underdose | |
| 125295293 | 12529529 | 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 |
|---|---|---|---|---|---|---|
| 125295293 | 12529529 | 1 | 2013 | 0 | ||
| 125295293 | 12529529 | 2 | 2013 | 0 | ||
| 125295293 | 12529529 | 3 | 2013 | 0 |