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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123235285 | 12323528 | 5 | F | 20160817 | 20160502 | 20160825 | EXP | US-ASTRAZENECA-2016SE44458 | ASTRAZENECA | 0.00 | M | Y | 72.60000 | KG | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123235285 | 12323528 | 1 | PS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | 202450 | 400 | UG | INHALATION POWDER | Q12H | |||||||
| 123235285 | 12323528 | 2 | SS | TUDORZA PRESSAIR | ACLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | 202450 | 400 | UG | INHALATION POWDER | Q12H | |||||||
| 123235285 | 12323528 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160MCG /4.5 MCG, TWO PUFFS, EVERY 12 HOURS | 0 | Q12H | |||||||||
| 123235285 | 12323528 | 4 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | AS REQUIRED | 0 | |||||||||||
| 123235285 | 12323528 | 5 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | 0 | 200 | MG | QD | |||||||||
| 123235285 | 12323528 | 6 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | 0 | 200 | MG | QD | |||||||||
| 123235285 | 12323528 | 7 | C | OXYGEN. | OXYGEN | 1 | 2 LITERS | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123235285 | 12323528 | 1 | Chronic obstructive pulmonary disease |
| 123235285 | 12323528 | 2 | Emphysema |
| 123235285 | 12323528 | 3 | Emphysema |
| 123235285 | 12323528 | 5 | Depression |
| 123235285 | 12323528 | 6 | Insomnia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123235285 | 12323528 | OT |
| 123235285 | 12323528 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123235285 | 12323528 | Chest pain | |
| 123235285 | 12323528 | Drug dose omission | |
| 123235285 | 12323528 | Drug effect decreased | |
| 123235285 | 12323528 | Dyspnoea | |
| 123235285 | 12323528 | Dyspnoea exertional | |
| 123235285 | 12323528 | Intentional product misuse | |
| 123235285 | 12323528 | Pneumonia | |
| 123235285 | 12323528 | Product packaging quantity issue | |
| 123235285 | 12323528 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 123235285 | 12323528 | 1 | 2014 | 0 | ||
| 123235285 | 12323528 | 2 | 2014 | 0 | ||
| 123235285 | 12323528 | 3 | 2014 | 0 | ||
| 123235285 | 12323528 | 4 | 2014 | 0 |