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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125671931 | 12567193 | 1 | I | 20160629 | 20160713 | 20160718 | 20160718 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-46015BP | BOEHRINGER INGELHEIM | 82.19 | YR | F | Y | 0.00000 | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125671931 | 12567193 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 150 MG | 22512 | 75 | MG | CAPSULE | BID | ||||||
| 125671931 | 12567193 | 2 | C | ALENDRONATE | ALENDRONATE SODIUM | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 3 | C | CARTIA XT | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 4 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 5 | C | FLUTICASONE | FLUTICASONEFLUTICASONE PROPIONATE | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 6 | C | FOSAMAX | ALENDRONATE SODIUM | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 7 | C | LASIX | FUROSEMIDE | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 8 | C | LANOXIN | DIGOXIN | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 9 | C | LOPRESSOR | METOPROLOL TARTRATE | 1 | Unknown | 2 ANZ | 0 | BID | |||||||||
| 125671931 | 12567193 | 10 | C | MULTIVITAMIN | VITAMINS | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 11 | C | POTASSIUM | POTASSIUM | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 12 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 6 ANZ | 0 | ||||||||||
| 125671931 | 12567193 | 13 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 0 | |||||||||||
| 125671931 | 12567193 | 14 | C | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | 1 ANZ | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125671931 | 12567193 | 1 | Atrial fibrillation |
| 125671931 | 12567193 | 2 | Bone disorder |
| 125671931 | 12567193 | 3 | Product used for unknown indication |
| 125671931 | 12567193 | 4 | Product used for unknown indication |
| 125671931 | 12567193 | 5 | Product used for unknown indication |
| 125671931 | 12567193 | 6 | Product used for unknown indication |
| 125671931 | 12567193 | 7 | Joint swelling |
| 125671931 | 12567193 | 8 | Gastrooesophageal reflux disease |
| 125671931 | 12567193 | 9 | Product used for unknown indication |
| 125671931 | 12567193 | 10 | Product used for unknown indication |
| 125671931 | 12567193 | 11 | Product used for unknown indication |
| 125671931 | 12567193 | 12 | Pain |
| 125671931 | 12567193 | 13 | Gastrooesophageal reflux disease |
| 125671931 | 12567193 | 14 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125671931 | 12567193 | HO |
| 125671931 | 12567193 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125671931 | 12567193 | Asthenia | |
| 125671931 | 12567193 | Fall | |
| 125671931 | 12567193 | Fatigue | |
| 125671931 | 12567193 | Myocardial infarction |
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 |
|---|---|---|---|---|---|---|
| 125671931 | 12567193 | 1 | 201404 | 0 |