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Cadictin (Cyproheptadine)

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Cadictin hydrochloride (CH) is a first-generation antihistamine which is used as an appetite stimulant. This study was designed to identify the role of CH therapy on weight gain, linear growth and body mass index in children with mild to moderate undernutrition.

Other names for this medication:
Actin, Apenorm, Apeplus, Apewin, Aptaur, Aptic, Becyp, Cynoc, Cyper, Cyperton, Cypomax, Cypratin, Cyprodol, Cyprolite, Cyprotol, Decyp, Hepoline, Hungree, Indocyp, Monic, Normatone, Oycip, Pepller, Polyactin, Prohep, Rarritol, Sycyp, Toractin

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Also known as: Cyproheptadine


Generic Cadictin is used to treat fever, nasal inflammation, stuffy nose, red and inflamed eyes, hives, swelling and other symptoms of cold and allergy. Generic Cadictin blocks the effects of the naturally occurring chemical histamine in your body. Cadictin is also known as Cyproheptadine, Ciplactin, Cadictine, Ciproral. Generic name of Generic Cadictin is Cyproheptadine. Brand name of Generic Cadictin is Cadictin.


Generic Cadictin can be taken in tablets (4mg) and syrup. You should take it by mouth. Take Generic Cadictin by mouth with or without food. Measure the syrup form of Generic Cadictin with a special dose-measuring spoon or cup. If you want to achieve most effective results do not stop taking Generic Cadictin suddenly.


If you overdose Generic Cadictin and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Generic Cadictin overdosage: extreme sleepiness, confusion, weakness, ringing in the ears, blurred vision, large pupils, dry mouth, flushing, fever, shaking, insomnia, hallucinations, seizure.


Store at room temperature between 15 to 30 degrees C (59 to 86 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Cadictin are:

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Do not take Generic Cadictin if you are allergic to Generic Cadictin components. Try to be careful with Generic Cadictin if you're pregnant or you plan to have a baby, or you are a nursing mother. Generic Cadictin can harm your baby. Do not take cyproheptadine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. Be careful in taking Generic Cadictin if you have glaucoma or pressure in the eye, stomach ulcer, enlarged prostate, bladder problems, difficulty urinating, hyperthyroidism, hypertension, any problems with heart, asthma. Be careful with taking Generic Cadictin if you use anxiety or sleep medicines such as alprazolam (Xanax), diazepam (Valium), chlordiazepoxide (Librium), temazepam (Restoril), or triazolam (Halcion); anti-depression medications such as amitriptyline (Elavil), doxepin (Sinequan), nortriptyline (Pamelor), fluoxetine (Prozac), sertraline (Zoloft), or paroxetine (Paxil); any other medications that make you feel drowsy, sleepy, or relaxed. Avoid machine driving while taking Generic Cadictin. Avoid alcohol. Do not stop taking Generic Cadictin suddenly.

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Interaction of the A alpha Y and Z mating-type homeodomain proteins of Schizophyllum commune detected by the two-hybrid system. Factors that influence clinical outcome following ACI for treatment of cartilage defects of the knee include patient-specific parameters on the one hand, such as body mass index, nicotine abusus, patients age, prior surgical treatment, duration of symptoms and more, and defect characteristics such as containment, defect location, defect size, number of defects treated, on the other hand. A 12-year-old girl with a 10-year history of a subcutaneous mass on the left gluteus measuring 4.5x4x3 cm had been referred. The PL1pro-mediated cleavage was albenza dose children slow and significantly suppressed by a non-proteolytic activity of PL2pro. Excessive bile acid activated NF-kappa B and promoted the development of alcoholic steatohepatitis in farnesoid X receptor deficient mice. Peroxide value of heated oil, histopathological alterations, antioxidant enzyme levels and blood biochemistry were determined in Wistar rats treated with the RHCO. The total amount of salivary IgA was determined by an immunobead enzyme-linked immunosorbent assay, and SDS-PAGE and Western blot analysis was performed using sonicated antigens of Streptococcus mutans and Streptococcus sobrinus strains and, as a control, a Streptococcus parasanguis strain. This is an important issue to address if a prolonged course of IGF-I is to be used clinically in muscle-wasting conditions where satellite cells may become limiting.

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