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Atheroz (Clopidogrel)
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Atheroz

Atheroz is an antiplatelet medication. It prevents your platelets from clumping together into blood clots. This can lower the risk of heart attack, since most heart attacks are caused by a clot forming in the vessels supplying your heart. Atheroz also lowers the risk of stroke, since most strokes are caused by blood clots in the vessels supplying your brain.

Other names for this medication:
Adplatt, Antiban, Antiplar, Antiplatt, Aplatin, Atheroz, Blothin, Caplor, Cidogrel, Clopact, Clopicard, Clopicure, Clopione, Clopiriv, Clopitab, Clopivas, Clopod, Cloprez, Clotsafe, Complatt, Deplatt, Dospin, Ecosprin, Livigrel, Neogrel, Nugrel, Plagerine, Plagril, Platfree, Platfrin, Platloc, Plodrel, Rosumac, Starclop, Synplatt, Themigril, Thrombosprin

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Also known as: Clopidogrel

Description

Atheroz target is the treatment of heart attacks and strokes by preventing blood clots. It is also taken to prevent other heart or blood vessels disorders. Atheroz is acting by preventing blood clots. It is antiplatelet agents. Atheroz is also known as Clopidogrel, Clopitab, Caplor, Iscover, Clopilet, Ceruvin. Generic name of Atheroz is Clopidogrel. Brand name of Atheroz is Atheroz.

Dosage

Usual Adult Dose for Acute Coronary Syndrome:

Unstable Angina (UA)/Non-ST-Elevation Myocardial Infarction (NSTEMI): -Loading dose: 300 mg orally once -Maintenance dose: 75 mg orally once a day -Duration of therapy: Optimal duration unknown. ST-Elevation Myocardial Infarction (STEMI): -Loading dose: 300 mg orally once (OPTIONAL) -Maintenance dose: 75 mg orally once a day, with or without thrombolytics -Duration of therapy: Optimal duration unknown. Comments: -Administer this drug in combination with aspirin 75 mg to 325 mg orally once a day. -The benefit of this drug for patients who undergo primary percutaneous coronary intervention is unknown. Uses: Prevention of atherothrombotic events in patients with non-ST-segment elevation acute coronary syndrome (UA, NSTEMI, those who are to be managed medically, those who are to be managed with coronary revascularization) and STEMI.

Usual Adult Dose for Ischemic Stroke:

75 mg orally once a day Uses: Prevention of atherothrombotic events in patients with a history of recent myocardial infarction, recent stroke, or established peripheral arterial disease.

Usual Adult Dose for Myocardial Infarction:

75 mg orally once a day Uses: Prevention of atherothrombotic events in patients with a history of recent myocardial infarction, recent stroke, or established peripheral arterial disease.

Usual Adult Dose for Peripheral Arterial Disease:

75 mg orally once a day Uses: Prevention of atherothrombotic events in patients with a history of recent myocardial infarction, recent stroke, or established peripheral arterial disease.

Detailed Atheroz dosage information

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Overdose can cause excessive bleeding.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Atheroz are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

You should not use Atheroz if you are allergic to clopidogrel, or if you have:

any active bleeding; or a stomach ulcer or bleeding in the brain (such as from a head injury).

Tell your doctor if you have ever had:

an ulcer in your stomach or intestines; or a bleeding disorder or blood clotting disorder.

Atheroz may not work as well if you have certain genetic factors that affect the breakdown of this medicine in your body. Your doctor may perform a blood test to make sure Atheroz is right for you.

This medicine is not expected to harm an unborn baby. Tell your doctor if you are pregnant.

You should not breastfeed while using this medicine.

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The sequences of PTH1R gene was retrieved from Genbank, and 4 pairs of oligonucleotides were synthesized and inserted into pSUPERretro RNAi, which was identified by RT-PCR and sequence analysis. The authors determined the 2D skin dose distributions, isodose curves, and cross-sectional profiles at the surface layers with or without the immobilization/support device. After exposure to CDDP in G1 phase, PC-9 cells were arrested in G2 phase. Torque history of electrically stimulated human quadriceps: implications for stimulation therapy. The effects of NMCs were examined by MC-NMC co-culture or incubating pure MCs in NMC-conditioned growth medium (NCGM). Thus, efforts aimed at enhancing protective immunity at these sites are a top priority, including increasing virus-specific antibodies (Abs) and antiviral activity at mucosal sites. Comparative assessment of remote results of the Billroth I and Billroth II gastric resections in stomach and duodenal ulcers. The CRG1 gene required for resistance to the singlet oxygen-generating cercosporin toxin in Cercospora nicotianae encodes a putative fungal transcription factor. Measurement of urinary tryptophan metabolites by reverse-phase high-pressure liquid chromatography. Our results indicate that the internal motions of the Rml and Rml complexes occur in a subspace of only a few degrees of freedom.

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Deferred treatment of low grade stage T3 prostate cancer without distant metastases. CGS 16949A, an aromatase inhibitor, was administered orally to female rats at doses of 1 and 10 mg/kg/day alone and in combination with tamoxifen (0.5 or 5 mg/kg/day) or 5-fluorouracil (20 mg/kg/day) for 14 days. Sonicated cashew apple bagasse showed higher antioxidant activity, higher total phenolic compounds (TPC) and higher vitamin C content when compared to the non-sonicated sample. A protein consisting of a subunit with molecular mass of 90 kDa was shown to bind to KS type GST 3-3 but not to NC type. Time to treatment failure, adverse events, the duration of chemotherapy holiday and quality of life were also evaluated. Neither the mean blood glucose values nor the mean cerebral glucose values predicted the outcome at 3 months. A frequent and large difference between the number of diphtheria and tetanus toxoids and pertussis vaccine doses administered in the two levels was detected.

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