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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125182212 | 12518221 | 2 | F | 201606 | 20160725 | 20160630 | 20160801 | PER | US-ASTRAZENECA-2016SE68456 | ASTRAZENECA | 897.00 | MON | F | Y | 59.00000 | KG | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125182212 | 12518221 | 1 | PS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | 24400 | UG | 1155398 | 202450 | 400 | UG | INHALATION POWDER | BID | ||||
| 125182212 | 12518221 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | SYMBICORT 160-4.5 MCG, 2 PUFFS, TWICE A DAY | 0 | ||||||||||
| 125182212 | 12518221 | 3 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | DAILY, 108 MCG, 2 PUFFS IN THE MORNING. | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125182212 | 12518221 | 1 | Chronic obstructive pulmonary disease |
| 125182212 | 12518221 | 2 | Chronic obstructive pulmonary disease |
| 125182212 | 12518221 | 3 | Chronic obstructive pulmonary disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125182212 | 12518221 | Anxiety | |
| 125182212 | 12518221 | Confusional state | |
| 125182212 | 12518221 | Device malfunction | |
| 125182212 | 12518221 | Drug dose omission | |
| 125182212 | 12518221 | Fatigue | |
| 125182212 | 12518221 | Intentional product misuse |
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 |
|---|---|---|---|---|---|---|
| 125182212 | 12518221 | 1 | 201605 | 0 |