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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121967272 | 12196727 | 2 | F | 201602 | 20160616 | 20160321 | 20160817 | PER | US-ASTRAZENECA-2016SE27537 | ASTRAZENECA | 749.00 | MON | M | Y | 86.20000 | KG | 20160818 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121967272 | 12196727 | 1 | PS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | 400 MCG, 1 PUFF TWICE A DAY | U | 202450 | INHALATION POWDER | ||||||||
| 121967272 | 12196727 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5MCG, 2 PUFFS TWICE A DAY | U | 0 | BID | ||||||||
| 121967272 | 12196727 | 3 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | AS REQUIRED NO MORE THAN 1 PUFF EVERY 4 HOURS | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121967272 | 12196727 | 1 | Asthma |
| 121967272 | 12196727 | 2 | Asthma |
| 121967272 | 12196727 | 3 | Asthma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121967272 | 12196727 | Agitation | |
| 121967272 | 12196727 | Cataract | |
| 121967272 | 12196727 | Chest discomfort | |
| 121967272 | 12196727 | Cold sweat | |
| 121967272 | 12196727 | Device failure | |
| 121967272 | 12196727 | Drug dose omission | |
| 121967272 | 12196727 | Drug hypersensitivity | |
| 121967272 | 12196727 | Dyspnoea | |
| 121967272 | 12196727 | Hot flush | |
| 121967272 | 12196727 | Intentional product misuse | |
| 121967272 | 12196727 | Nasopharyngitis | |
| 121967272 | 12196727 | Nervousness | |
| 121967272 | 12196727 | Off label use | |
| 121967272 | 12196727 | Open angle glaucoma | |
| 121967272 | 12196727 | Panic attack | |
| 121967272 | 12196727 | Product use issue | |
| 121967272 | 12196727 | Underdose | |
| 121967272 | 12196727 | Vision blurred | |
| 121967272 | 12196727 | Visual impairment | |
| 121967272 | 12196727 | Weight increased | |
| 121967272 | 12196727 | Withdrawal syndrome |
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 |
|---|---|---|---|---|---|---|
| 121967272 | 12196727 | 1 | 201502 | 0 | ||
| 121967272 | 12196727 | 2 | 201502 | 0 | ||
| 121967272 | 12196727 | 3 | 201502 | 0 |