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Cozaar(Losartan Potassium Tablets)(十六)
2016-08-27 09:05:29 来源: 作者: 【 】 浏览:8397次 评论:0
  
Cataract
   Sinusitis
7
6
5
5
Hemic
   Anemia
14
11
Metabolic and Nutrition
   Hyperkalemia
   Hypoglycemia
   Weight gain
7
14
4
3
10
3
Musculoskeletal
   Back pain
   Leg pain
   Knee pain
   Muscular weakness
12
5
5
7
10
4
4
4
Nervous System
   Hypesthesia
5
4
Respiratory
   Bronchitis
   Cough
10
11
9
10
Skin
   Cellulitis
7
6
Urogenital
   Urinary tract infection
16
13
Post-Marketing Experience
The following additional adverse reactions have been reported in post-marketing experience:

Digestive: Hepatitis (reported rarely).

General disorders and administration site conditions: Malaise.

Hemic: Thrombocytopenia (reported rarely).

Hypersensitivity: Angioedema, including swelling of the larynx and glottis, causing airway obstruction and/or swelling of the face, lips, pharynx, and/or tongue has been reported rarely in patients treated with losartan; some of these patients previously experienced angioedema with other drugs including ACE inhibitors. Vasculitis, including Henoch-Schönlein purpura, has been reported. Anaphylactic reactions have been reported.

Metabolic and Nutrition: Hyperkalemia, hyponatremia have been reported with losartan.

Musculoskeletal: Rare cases of rhabdomyolysis have been reported in patients receiving angiotensin II receptor blockers.

Nervous system disorders: Dysgeusia

Respiratory: Dry cough (see above).

Skin: Erythroderma


Laboratory Test Findings
In controlled clinical trials, clinically important changes in standard laboratory parameters were rarely associated with administration of COZAAR.

Creatinine, Blood Urea Nitrogen: Minor increases in blood urea nitrogen (BUN) or serum creatininewere observed in less than 0.1 percent of patients with essential hypertension treated with COZAAR alone (see PRECAUTIONS, Impaired Renal Function).

Hemoglobin and Hematocrit: Small decreases in hemoglobin and hematocrit (mean decreases of approximately 0.11 grams percent and 0.09 volume percent, respectively) occurred frequently in patients treated with COZAAR alone, but were rarely of clinical importance. No patients were discontinued due to anemia.

Liver Function Tests: Occasional elevations of liver enzymes and/or serum bilirubin have occurred. In patients with essential hypertension treated with COZAAR alone, one patient (<0.1%) was discontinued due to these laboratory adverse experiences.


OVERDOSAGE
Significant lethality was observed in mice and rats after oral administration of 1000 mg/kg and 2000 mg/kg, respectively, about 44 and 170 times the maximum recommended human dose on a mg/m2 basis.

Limited data are available in regard to overdosage in humans. The most likely manifestation of overdosage would be hypotension and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation. If symptomatic hypotension should occur, supportive treatment should be instituted.

Neither losartan nor its active metabolite can be removed by hemodialysis.


DOSAGE AND ADMINISTRATION

Adult Hypertensive Patients
COZAAR m

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