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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125786071 | 12578607 | 1 | I | 2013 | 20160623 | 20160721 | 20160721 | PER | US-PFIZER INC-2016316017 | PFIZER | 0.00 | F | Y | 106.59000 | KG | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125786071 | 12578607 | 1 | PS | TIKOSYN | DOFETILIDE | 1 | 500 MG, UNK | 20931 | 500 | MG | CAPSULE, HARD | ||||||||
| 125786071 | 12578607 | 2 | SS | TIKOSYN | DOFETILIDE | 1 | 250 MG, UNK | 20931 | 250 | MG | CAPSULE, HARD | ||||||||
| 125786071 | 12578607 | 3 | SS | TIKOSYN | DOFETILIDE | 1 | 500 MG, UNK | 20931 | 500 | MG | CAPSULE, HARD | ||||||||
| 125786071 | 12578607 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 37.5 MCG, 1X/DAY | 0 | 37.5 | UG | QD | ||||||||
| 125786071 | 12578607 | 5 | C | KLOR-CON M20 | POTASSIUM CHLORIDE | 1 | Oral | 1 TABLET, DAILY | 0 | 1 | DF | TABLET | |||||||
| 125786071 | 12578607 | 6 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 40 MG, 1X/DAY | 0 | 40 | MG | QD | ||||||||
| 125786071 | 12578607 | 7 | C | ELIQUIS | APIXABAN | 1 | 5 MG, 2X/DAY | 0 | 5 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125786071 | 12578607 | 1 | Atrial fibrillation |
| 125786071 | 12578607 | 4 | Thyroid mass |
| 125786071 | 12578607 | 5 | Routine health maintenance |
| 125786071 | 12578607 | 6 | Gastrooesophageal reflux disease |
| 125786071 | 12578607 | 7 | Anticoagulant therapy |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125786071 | 12578607 | Apathy | |
| 125786071 | 12578607 | Disturbance in attention | |
| 125786071 | 12578607 | Dizziness | |
| 125786071 | 12578607 | Drug ineffective | |
| 125786071 | 12578607 | Fatigue | |
| 125786071 | 12578607 | Lethargy | |
| 125786071 | 12578607 | Musculoskeletal stiffness |
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 |
|---|---|---|---|---|---|---|
| 125786071 | 12578607 | 5 | 2013 | 0 |