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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126630451 | 12663045 | 1 | I | 20160501 | 20160809 | 20160818 | 20160818 | EXP | US-DRREDDYS-USA/USA/16/0082333 | DR REDDYS | 64.47 | YR | F | Y | 0.00000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126630451 | 12663045 | 1 | PS | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Unknown | U | U | UNKNOWN | 50564 | ||||||||
| 126630451 | 12663045 | 2 | SS | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | 6ZP3857 | 0 | INHALATION POWDER | |||||||||
| 126630451 | 12663045 | 3 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Unknown | F86D | 0 | INHALER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126630451 | 12663045 | 1 | Product used for unknown indication |
| 126630451 | 12663045 | 2 | Emphysema |
| 126630451 | 12663045 | 3 | Emphysema |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126630451 | 12663045 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126630451 | 12663045 | Adverse drug reaction | |
| 126630451 | 12663045 | Dehydration | |
| 126630451 | 12663045 | Feeling abnormal | |
| 126630451 | 12663045 | Surgery |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |