Hyperlipidemia
Conditions
Interventions
investigational material(s)
Generic name etc : Polyunsaturated Fatty Acids
INN of investigational material : -
Therapeutic category code : 218 Agents for hyperlipidemias
Dosage and Administration for
Sponsors
Takeda Pharmaceutical Company Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Patients with hyperlipidemia diagnosis are prescribed at least one polyunsaturated fatty acid (PUFA) prescription during the study period. - Patients aged 20 years or more - Patients received the serum test of n-3 and n-6 PUFA at least one or more times during the study period.
Exclusion criteria
Exclusion criteria: -
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| other Blood levels of n-3 and n-6 PUFA before and after PUFA the index date. | — |
Secondary
| Measure | Time frame |
|---|---|
| other Changes in serum levels of n-3 and n-6 PUFA from the baseline in patients treated with PUFA. other Change in HbA1c, total cholesterol, LDL cholesterol, HDL cholesterol, RLP cholesterol, apoprotein B-48, and hs-CRP before and after treatment | — |
Countries
Japan
Outcome results
None listed