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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126300181 | 12630018 | 1 | I | 20160703 | 20160728 | 20160808 | 20160808 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-49750BP | BOEHRINGER INGELHEIM | 64.02 | YR | F | Y | 0.00000 | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126300181 | 12630018 | 1 | PS | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | DOSE PER APPLICATION AND DAILY DOSE: 20 MCG/100 MCG | U | 21747 | PRESSURISED INHALATION | ||||||||
| 126300181 | 12630018 | 2 | SS | ATROVENT | IPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | 17 MCG | U | 21527 | 17 | UG | INHALATION SOLUTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126300181 | 12630018 | 1 | Product used for unknown indication |
| 126300181 | 12630018 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126300181 | 12630018 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126300181 | 12630018 | Oxygen saturation decreased | |
| 126300181 | 12630018 | Panic attack |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |