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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124834133 | 12483413 | 3 | F | 20160913 | 20160621 | 20160914 | PER | PHEH2016US014907 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124834133 | 12483413 | 1 | PS | TEKTURNA | ALISKIREN HEMIFUMARATE | 1 | Unknown | 150 MG, QD | 21985 | 150 | MG | TABLET | QD | ||||||
| 124834133 | 12483413 | 2 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | U | 0 | ||||||||||
| 124834133 | 12483413 | 3 | C | VITA B | 2 | Unknown | U | 0 | |||||||||||
| 124834133 | 12483413 | 4 | C | VITAMIN C | ASCORBIC ACID | 1 | Unknown | U | 0 | ||||||||||
| 124834133 | 12483413 | 5 | C | FLAXSEED | FLAX SEED | 1 | Unknown | U | 0 | ||||||||||
| 124834133 | 12483413 | 6 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124834133 | 12483413 | 1 | Product used for unknown indication |
| 124834133 | 12483413 | 2 | Product used for unknown indication |
| 124834133 | 12483413 | 3 | Product used for unknown indication |
| 124834133 | 12483413 | 4 | Product used for unknown indication |
| 124834133 | 12483413 | 5 | Product used for unknown indication |
| 124834133 | 12483413 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124834133 | 12483413 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124834133 | 12483413 | Blood pressure inadequately controlled | |
| 124834133 | 12483413 | Blood pressure increased | |
| 124834133 | 12483413 | Drug hypersensitivity | |
| 124834133 | 12483413 | Feeling abnormal | |
| 124834133 | 12483413 | Headache | |
| 124834133 | 12483413 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |