b=Ll$m�V��1]vܵ������&�H6foF���n�-1�Jfwh�9�����'�������1��K��|��X�ϱ)�j6*�g4�P��P�o���-��;������{G��w�@�b�� These studies had a treatment duration of up to 12 weeks.Other adverse reactions reported in clinical studies were abdominal pain, dizziness, hypersensitivity (including rash, pruritus, urticaria, and angioedema) and pancreatitis. This patient also experienced Grade 3 adverse events of acute respiratory failure, cellulitis and asthenia (considered serious).

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However, the safety and effectiveness of Crestor were evaluated in a two year open-label uncontrolled trial that included children and adolescents 8 to 17 years of age with heterozygous familial hypercholesterolemia Children and adolescents 7 to 15 years of age with homozygous familial hypercholesterolemia were studied in a 6-week randomized, placebo-controlled, cross-over study with Crestor 20 mg once daily followed by 12 weeks of open-label treatment Although not all adverse reactions identified in the adult population have been observed in clinical trials of children and adolescent patients, the same warnings and precautions for adults should be considered for children and adolescents.
In the JUPITER study, 17,802 participants were treated with rosuvastatin 20 mg (n=8901) or placebo (n=8901) for a mean duration of 2 years. The 7 patients not enrolled did not meet all inclusion and exclusion criteria (3 patients had cirrhosis but did not have liver imaging within 6 months to exclude hepatocellular carcinoma, 4 patients had exclusionary medical history or were not in general good health, 2 patients had laboratory parameters outside acceptable ranges, 1 patient had clinically relevant alcohol or drug abuse within 12 months prior to screening and 1 patient had not received a prior HCV treatment regimen required for enrolment).

Corneal opacity was seen in dogs treated for 52 weeks at 6 mg/kg/day by oral gavage (systemic exposures 20 times the human exposure at 40 mg/day based on AUC).

�e�X5y���A�5Vb�f�Mu����Q��B�EHm�ӕ`�E�|�+� x������`Y���V��UC&��\JD�p�5�pT�,������2Ϡ/��BY%��M^S�;�t\��e�^d��! You may report side effects to FDA at 1-800-FDA-1088.Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. ���Q�-@� ZgS There was no detectable effect of Crestor on growth, weight, BMI (body mass index), or sexual maturation Crestor has not been studied in controlled clinical trials involving prepubertal patients or patients younger than 10 years of age with heterozygous familial hypercholesterolemia. Especially clopidogrel and ticagrelor are drugs of which the potential drug-interactions are complex and hard to manage.

Chronic alcohol liver disease is known to increase rosuvastatin exposure; Crestor should be used with caution in these patients Pharmacokinetic studies have demonstrated an approximate 2‑fold increase in median exposure to rosuvastatin in Asian subjects when compared with Caucasian controls.

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