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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126336892 | 12633689 | 2 | F | 2014 | 20160809 | 20160809 | 20160818 | EXP | US-TEVA-681655USA | TEVA | 0.00 | F | Y | 54.48000 | KG | 20160818 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126336892 | 12633689 | 1 | PS | PROAIR HFA | ALBUTEROL SULFATE | 1 | 2 PUFFS THREE TIMES A DAY | U | DAC20A | 21457 | |||||||||
| 126336892 | 12633689 | 2 | SS | PROAIR HFA | ALBUTEROL SULFATE | 1 | U | DAC20A | 21457 | ||||||||||
| 126336892 | 12633689 | 3 | C | ALBUTEROL NEBULIZER | ALBUTEROL | 1 | 0 | ||||||||||||
| 126336892 | 12633689 | 4 | C | ALBUTEROL NEBULIZER | ALBUTEROL | 1 | 0 | ||||||||||||
| 126336892 | 12633689 | 5 | C | BISOPROLOL FUMARATE. | BISOPROLOL FUMARATE | 1 | 0 | ||||||||||||
| 126336892 | 12633689 | 6 | C | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | 0 | ||||||||||||
| 126336892 | 12633689 | 7 | C | PREDNISONE. | PREDNISONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126336892 | 12633689 | 1 | Chronic obstructive pulmonary disease |
| 126336892 | 12633689 | 2 | Hypersensitivity |
| 126336892 | 12633689 | 3 | Chronic obstructive pulmonary disease |
| 126336892 | 12633689 | 4 | Hypersensitivity |
| 126336892 | 12633689 | 5 | Cardiac disorder |
| 126336892 | 12633689 | 7 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126336892 | 12633689 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126336892 | 12633689 | Blindness | |
| 126336892 | 12633689 | Cataract | |
| 126336892 | 12633689 | Dyspnoea | |
| 126336892 | 12633689 | Eye haemorrhage | |
| 126336892 | 12633689 | Gastrointestinal haemorrhage | |
| 126336892 | 12633689 | Inappropriate schedule of drug administration | |
| 126336892 | 12633689 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 126336892 | 12633689 | 1 | 2010 | 0 |