The study will focus on effectiveness and safety of rivaroxaban (Xarelto) when given together with acetylsalicylic acid (combination therapy) to patients suffering from coronary artery disease (a condition that affects the blood vessels supplying the heart) and / or peripheral artery disease (a condition that affects the blood vessels of the lower limbs) in the routine clinical practice. The study will help to collect data for prevention cardiovascular death, myocardial infarction (MI), stroke and major adverse limb events in adult patients. The study will focus on information on when and why physicians are starting to treat patients with combination therapy, treatment duration, reasons to discontinue treatment and previous therapies. The study will also investigate treatment outcomes for patients being treated with a combination therapy by their physicians.
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Health status by questionnaire EQ-5D-5L
Timeframe: Up to 34 months
Descriptive analysis of clinical characteristics of CAD participants
Timeframe: At baseline
Descriptive analysis of clinical characteristics of PAD participants
Timeframe: At baseline
Descriptive analysis of prior antithrombotic treatment
Timeframe: At baseline
Descriptive analysis of concomitant antithrombotic treatment
Timeframe: Upto 34 months
Descriptive analysis of prior secondary prevention therapies
Timeframe: At baseline
Descriptive analysis of concomitant secondary prevention therapies
Timeframe: Up to 34 months
Reason to start rivaroxaban
Timeframe: At baseline
Decision point to start rivaroxaban
Timeframe: At baseline
Reasons for discontinuation of rivaroxaban
Timeframe: Up to 34 months
Planned duration of treatment with rivaroxaban
Timeframe: At baseline
Actual duration of treatment with rivaroxaban
Timeframe: Up to 34 months
Planned duration of treatment with Acetylsalicylic acid (ASA)
Timeframe: At baseline
Actual duration of treatment with ASA
Timeframe: Up to 34 months