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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122426672 | 12242667 | 2 | F | 20160921 | 20160406 | 20160928 | EXP | US-VALIDUS PHARMACEUTICALS LLC-US-2016VAL000667 | VALIDUS | 0.00 | F | Y | 0.00000 | 20160928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122426672 | 12242667 | 1 | PS | METOPROLOL. | METOPROLOL | 1 | UNK | U | 17963 | ||||||||||
| 122426672 | 12242667 | 2 | SS | METOPROLOL. | METOPROLOL | 1 | UNK | U | 17963 | ||||||||||
| 122426672 | 12242667 | 3 | SS | METOPROLOL. | METOPROLOL | 1 | HALF TAB | U | 17963 | ||||||||||
| 122426672 | 12242667 | 4 | C | COZAAR | LOSARTAN POTASSIUM | 1 | 100 MG, (IN THE MORNING ) | U | 0 | 100 | MG | TABLET | |||||||
| 122426672 | 12242667 | 5 | C | REQUIP | ROPINIROLE HYDROCHLORIDE | 1 | 1.05 MG, TID (MORNING, NOON AND BEDTIME) | U | 0 | 1.05 | MG | TABLET | |||||||
| 122426672 | 12242667 | 6 | C | CALCIUM | CALCIUM | 1 | UNK | U | 0 | ||||||||||
| 122426672 | 12242667 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 1500 MG, BID | U | 0 | 1500 | MG | CAPSULE | |||||||
| 122426672 | 12242667 | 8 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 1 DF,( IN THE MORNING) | U | 0 | 1 | DF | CAPSULE | |||||||
| 122426672 | 12242667 | 9 | C | COUMADIN | WARFARIN SODIUM | 1 | 2 DF, UNK (2, 2.5 MG CAPLETS ON SUNDAY AND THURSDAY) | U | 0 | 2 | DF | ||||||||
| 122426672 | 12242667 | 10 | C | FLOVENT | FLUTICASONE PROPIONATE | 1 | UNK , BID (2 PUFFS IN THE MORNING, 2 PUFFS AT BEDTIME) | U | 0 | INHALER | |||||||||
| 122426672 | 12242667 | 11 | C | MECLIZINE | MECLIZINE HYDROCHLORIDE | 1 | UNK, PRN | U | 0 | ||||||||||
| 122426672 | 12242667 | 12 | C | MECLIZINE | MECLIZINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 122426672 | 12242667 | 13 | C | ONDANSETRON | ONDANSETRON | 1 | UNK | U | 0 | ||||||||||
| 122426672 | 12242667 | 14 | C | COMPAZINE | PROCHLORPERAZINE MALEATE | 1 | UNK | U | 0 | ||||||||||
| 122426672 | 12242667 | 15 | C | COMPAZINE | PROCHLORPERAZINE MALEATE | 1 | U | 0 | |||||||||||
| 122426672 | 12242667 | 16 | C | OXYCODONE | OXYCODONE | 1 | UNK, PRN | U | 0 | ||||||||||
| 122426672 | 12242667 | 17 | C | ALBUTEROL. | ALBUTEROL | 1 | UNK, PRN | U | 0 | INHALER | |||||||||
| 122426672 | 12242667 | 18 | C | PREDNISONE. | PREDNISONE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122426672 | 12242667 | 1 | Atrial fibrillation |
| 122426672 | 12242667 | 2 | Cardiac failure congestive |
| 122426672 | 12242667 | 4 | Product used for unknown indication |
| 122426672 | 12242667 | 5 | Restless legs syndrome |
| 122426672 | 12242667 | 6 | Product used for unknown indication |
| 122426672 | 12242667 | 7 | Product used for unknown indication |
| 122426672 | 12242667 | 8 | Product used for unknown indication |
| 122426672 | 12242667 | 9 | Product used for unknown indication |
| 122426672 | 12242667 | 10 | Product used for unknown indication |
| 122426672 | 12242667 | 11 | Dizziness |
| 122426672 | 12242667 | 12 | Ill-defined disorder |
| 122426672 | 12242667 | 13 | Nausea |
| 122426672 | 12242667 | 14 | Product used for unknown indication |
| 122426672 | 12242667 | 15 | Nausea |
| 122426672 | 12242667 | 16 | Arthralgia |
| 122426672 | 12242667 | 17 | Product used for unknown indication |
| 122426672 | 12242667 | 18 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122426672 | 12242667 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122426672 | 12242667 | Adverse event | |
| 122426672 | 12242667 | Drug interaction | |
| 122426672 | 12242667 | Fall | |
| 122426672 | 12242667 | Heart rate decreased | |
| 122426672 | 12242667 | Limb immobilisation | |
| 122426672 | 12242667 | Upper limb fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |