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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82005697 | 8200569 | 7 | F | 2011 | 20160826 | 20111026 | 20160831 | EXP | US-GLAXOSMITHKLINE-A0949716A | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82005697 | 8200569 | 1 | PS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 1 PUFF(S), PRN | 1ZP5739 | 20983 | 1 | DF | |||||||
| 82005697 | 8200569 | 2 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | UNK | F0598 | 20983 | ||||||||||
| 82005697 | 8200569 | 3 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 PUFF(S), PRN | 6ZP5076 | 20983 | 2 | DF | |||||||
| 82005697 | 8200569 | 4 | SS | FLOVENT | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | 1 PUFF, 2D | Y | F0015 | 0 | 1 | DF | BID | |||||
| 82005697 | 8200569 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK, U | U | 0 | |||||||||
| 82005697 | 8200569 | 6 | C | THEOPHYLLINE | THEOPHYLLINE ANHYDROUS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 82005697 | 8200569 | 1 | Productive cough |
| 82005697 | 8200569 | 2 | Traumatic lung injury |
| 82005697 | 8200569 | 4 | Productive cough |
| 82005697 | 8200569 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 82005697 | 8200569 | HO |
| 82005697 | 8200569 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 82005697 | 8200569 | Drug ineffective | |
| 82005697 | 8200569 | Dyspnoea | |
| 82005697 | 8200569 | Hospitalisation | |
| 82005697 | 8200569 | Incorrect dose administered | |
| 82005697 | 8200569 | Inhalation therapy | |
| 82005697 | 8200569 | Off label use | |
| 82005697 | 8200569 | Overdose | |
| 82005697 | 8200569 | Product quality issue | |
| 82005697 | 8200569 | Rib fracture | |
| 82005697 | 8200569 | Spinal compression fracture | |
| 82005697 | 8200569 | Spinal disorder | |
| 82005697 | 8200569 | Spinal fracture |
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 |
|---|---|---|---|---|---|---|
| 82005697 | 8200569 | 3 | 2010 | 0 | ||
| 82005697 | 8200569 | 4 | 201112 | 201206 | 0 |