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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121959932 | 12195993 | 2 | F | 201602 | 20160913 | 20160321 | 20160917 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-12367BP | BOEHRINGER INGELHEIM | 73.37 | YR | M | Y | 83.01000 | KG | 20160917 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121959932 | 12195993 | 1 | PS | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | 4 ANZ | 501785A,501785,15L0105 | 21747 | PRESSURISED INHALATION | QID | |||||||
| 121959932 | 12195993 | 2 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 4 ANZ | 0 | NEBULISER LIQUID | |||||||||
| 121959932 | 12195993 | 3 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 7 MG | 0 | 7 | MG | TABLET | QD | ||||||
| 121959932 | 12195993 | 4 | C | Benaspril | 2 | Oral | 40 MG | 0 | 20 | MG | TABLET | BID | |||||||
| 121959932 | 12195993 | 5 | C | METOPROLOL. | METOPROLOL | 1 | Oral | 100 MG | 0 | 50 | MG | TABLET | BID | ||||||
| 121959932 | 12195993 | 6 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Oral | DOSE PER APPLICATION AND DAILY DOSE: 10 MG / 325 MG | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121959932 | 12195993 | 1 | Chronic obstructive pulmonary disease |
| 121959932 | 12195993 | 2 | Chronic obstructive pulmonary disease |
| 121959932 | 12195993 | 3 | Product used for unknown indication |
| 121959932 | 12195993 | 4 | Hypertension |
| 121959932 | 12195993 | 5 | Hypertension |
| 121959932 | 12195993 | 6 | Intervertebral disc degeneration |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121959932 | 12195993 | Dyspnoea | |
| 121959932 | 12195993 | 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 |
|---|---|---|---|---|---|---|
| 121959932 | 12195993 | 1 | 20160125 | 0 | ||
| 121959932 | 12195993 | 2 | 2014 | 0 | ||
| 121959932 | 12195993 | 3 | 2012 | 0 | ||
| 121959932 | 12195993 | 4 | 2012 | 0 | ||
| 121959932 | 12195993 | 5 | 2012 | 0 | ||
| 121959932 | 12195993 | 6 | 201503 | 0 |