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Functions and indications: Use for wandering joint pain, pain in the limbs, vexing pain in the joints. Packing: 250mg X 100 pills per bottle. Caution: Do not use if pregnant. Contraindicated for the deficiency of vital energy and blood. It is a better treatment means to take it with other drugs for exterior use. Ingredients: Sichuan Teasel root, Pubescent Angelica root, Chinese Pine, Siler root, Large-Leaf Gentian root, Myrrh resin, Achyranthes root, Flowering Quince fruit, White Mulberry young twig, Dong Quai root Directions: Take 10 pills 2 times a day with warm water as a dietary supplement. This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Acetazolamide 250 mg, 100 Tablets Used primarily to treat hyperkalemic periodic paralysis (HYPP) in Quarter Horses, a genetic disease of the neuromuscular system. New Page 2 New Page 1 Acetazolamide 250mg, 100 Tablets Product Description: Used primarily to treat hyperkalemic periodic paralysis (HYPP), a genetic disease of the neuromuscular system. Also used to decrease intraocular pressure in the treatment of glaucoma in animals. Drug Class: Diuretic Adverse Effects: Acetazolamide can potentially produce hypkalemia in some patients. Contraindications , Precautions, and Drug Interactions: Do not use in patients with acidemia. Use with caution in any animals sensitive to sulfonamides. Small Animal Dosage Information: Dogs and Cats: For glaucoma: 5-10 mg/kg, Every 8-12 hours, by mouth. For other dosage information see your veterinarian. *When used to treat glaucoma, monitor patient's ocular pressure. New Page 1 What is HYPP? Hyperkalemic Periodic Paralysis Disease (HYPP) is a muscular disease that affects both horses and humans. It is caused by a hereditary genetic defect that disrupts a protein called a sodium ion channel, a tiny gateway in the membrane of muscle cells. The genetic defect disrupts the channel's normal opening and closing, such that uncontrolled sodium influxes occur. These influxes in turn change the voltage current of muscle cells, causing uncontrolled muscle twitching or profound muscle weakness. High levels of potassium in the blood usually are present when the disruptions in the ion channel occur. What Are Effects of HYPP? Horses with HYPP can experience unpredictable attacks of paralysis which, in severe cases, can lead to collapse and sudden death. The cause of death usually is cardiac arrest and /or respiratory failure. The disease is characterized by intermittent episodes of muscle tremors manifested by generalized or localized shaking, trembling and weakness. Occasionally, episodes are accompanied by respiratory noises resulting from paralysis of the muscles of the upper airway (larynx and pharynx). In cases of mild attacks, muscle tremors may be so subtle as to be detectable only by an experienced clinician performing EMG testing. Can Symptoms of HYPP Vary in Severity? Clinical signs of HYPP do vary widely among different horses. Homozygous horses are affected more severely than heterozygous horses. Under ideal management practices, the defective gene does not appear to have adverse effects, but stress and/or increased potassium in the serum can trigger clinical signs of muscle dysfunction. Why some horses manifest severe signs of the disease and other exhibit little or no signs is unknown but currently under investigation. Unfortunately, a horse carrying the defective gene but showing minimal signs has the same chance of passing the gene to future generations as does the affected horse with severe signs. What is the Origin of the Genetic Defect Causing HYPP? The original genetic defect causing HYPP was a natural mutation

CIRCULEX (TIAN MA) Functions and indications: To relive rheumatic conditions, alleviate muscle contracture, remove obstruction from collateral channels, promote blood circulation and relieve pain. Use for muscle contracture and numbness of the limbs, aching in the loins and legs. Packing: 250mg X 100 pills per bottle. Ingredients: Gastrodia rhizome 20.5mg, Achyranthes root 20.5mg, Ningpo Figwort root 20.5mg, Eucommia bark 24mg, Rhizoma Dioscoreae 20.5mg, Notopterygium root 36mg, Foxglove root 54.7mg, Tang Kwei root 36mg, Herba Duhuo root 17.3mg Directions: Take 9 pills 2 times a day as a dietary supplement. Warning: Do not use if you are pregnant. This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Dexamethasone Solution 2mg/mL, 100mL Dexamethasone is an corticosteroid given for its anti- inflammatory effects in a wide range of conditions. 2 mg/mL for Intravenous or Intramuscular Injection Veterinary CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. DESCRIPTION Dexamethasone is a synthetic analogue of prednisolone, having similar but more potent anti- inflammatory therapeutic action and diversified hormonal and metabolic effects. Modification of the basic corticoid structure as achieved in dexamethasone offers enhanced anti- inflammatory effect compared to older corticosteroids. The dosage of dexamethasone required is markedly lower than that of prednisone and prednisolone. Dexamethasone is not species- specific; however, the veterinarian should read the sections on INDICATIONS, DOSAGE, SIDE EFFECTS, CONTRAINDICATIONS , PRECAUTIONS and WARNING before this drug is used. Dexamethasone Solution is intended for intravenous or intramuscular administration. Each mL contains 2 mg dexamethasone, 500 mg polyethylene glycol 400, 9 mg benzyl alcohol, 1.8 mg methylparaben and 0.2 mg propylparaben as preservatives, 4.75% alcohol, HCl to adjust pH to approximately 4.9, water for injection q.s. EXPERIMENTAL STUDIES Experimental animal studies on dexamethasone have revealed it possesses greater anti- inflammatory activity than many steroids. Veterinary clinical evidence indicates dexamethasone has approximately twenty times the anti- inflammatory activity of prednisolone and seventy to eighty times that of hydrocortisone. Thymus involution studies show dexamethasone possesses twenty-five times the activity of prednisolone. In reference to mineralocorticoid activity, dexamethasone does not cause significant sodium or water retention. Metabolic balance studies show that animals on controlled and limited protein intake will exhibit nitrogen losses on exceedingly high dosages. INDICATIONS Dexamethasone Solution is indicated for the treatment of primary bovine ketosis and as an anti- inflammatory agent in the bovine and equine. As supportive therapy, dexamethasone may be used in the management of various rheumatic, allergic, dermatologic, and other diseases known to be responsive to anti- inflammatory corticosteroids. Dexamethasone Solution may be used intravenously as supportive therapy when an immediate hormonal response is required. Bovine Ketosis Dexamethasone Solution is offered for the treatment of primary ketosis. The gluconeogenic effects of dexamethasone, when administered intramuscularly, are generally noted within the first 6 to 12 hours. When Dexamethasone Solution is used intravenously, the effects may be noted sooner. Blood sugar levels rise to normal levels rapidly and generally rise to above normal levels within 12 to 24 hours. Acetone bodies are reduced to normal concentrations usually within 24 hours. The physical attitude of animals treated with dexamethasone brightens and appetite improves, usually within

HAEMELEX PILL(GUI LU BU) Functions and indications: Use for general weakness, headache, giddiness and dizziness, lumbago, pains in loins and knees. Ingredients: Testudinis 7.34mg, Pilose Antler 6.32mg, Rehmannia Root 37.1mg, Cornus fruit 7.32mg, Cistanche 6.32mg, Astragalus root 7.32mg, Codonopsis 7.32mg, Psoralea fruit 6.32mg, Chain fern 7.32mg, Epimedium 7.32mg Directions: Take 10 pills 2 times a day as a dietary supplement. Warning: Do not use if you are pregnant. 100 pills (250mg each) This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

AURICULAREX PILL (ER MING) Functions and indications: Use for weakness of liver, debility, vertigo, headache and auricular aibrillation. Packing: 250mg X 100 pills per bottle Caution: Do not use if pregnancy. Ingredients: Chinese Foxglove root 59.2mg, Cornus fruit 29.4mg, Chinese yam 29.4mg, Mouton root 22mg, China root 22mg, Alisma 22mg, Thorowax root 16mg Directions: Take 10 pills 2 times a day as a dietary supplement. This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

FRUCTUS SOPHORAE Gentlex Pill (HUAI JIAO) Functions and indications: To arrest bleeding by reducing heat from blood for treating hematochezia. Use for hematochezia, hemorrhoidal swelling and pain. Ingredients: Sophora fruit 57mg, Bitter orange fruit 28.6mg, Angelica root 28.6mg, Saposhinkovia 28.6mg, Scutellaria 28.6mg Directions: Take 8 pills 2 times a day as an herbal supplement. Warning: Do not use if you are pregnant. 100 pills (250mg each) This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Prednisone 20 mg, 500 Tablets Prednisone is used in the treatment of many disease processes including adrenal insufficiency, arthritis, lupus, allergies, asthma, dermatitis, blood and skin disorders. New Page 1 Prednisone 20 mg, 500 Tablets Prednisone is a synthetic corticosteroid used for many conditions.nbsp; Its anti- inflammatory activity is approximately four times that of hydrocortisone. Corticosteroids are extremely effective anti- inflammatory drugs because they affect the inflammatory process at so many different levels. Prednisone is rapidly converted to prednisolone in the liver and in most instances, these drugs are considered to be roughly equivalent.nbsp; Prednisone may be given by injection, orally or topically. Dogs and Cats:nbsp; Prednisone is used for a wide variety of conditions in both dogs and cats. It may be used in emergency situations including, anaphylactic reactions, spinal chord trauma, and many forms of shock. It is used in the management and treatment of immune mediated disease such as immune mediated hemolytic anemia, or thombocytopenia: many CNS disorders: some neoplasia: dermatologic diseases: allergic reactions such as asthma, hives, and itching: inflammatory orthopedic diseases: endocrine disorders including Addison's: respiratory disease with an inflammatory component, inflammatory bowel diseases and many other conditions.nbsp; Cats may require higher doses than dogs in order to achieve clinical response, but they are less likely to develop adverse side effects. Horses:nbsp; Prednisone is given systemically to decrease inflammatory and immune responses. For years it was used orally to treat Chronic Obstructive Pulmonary Disease (COPD), and other allergic or immune-mediated disorders. Recent studies show that horses do not absorb oral prednisone, but they do absorb oral prednisolone. Other corticosteroids are preferred for intra-articular use. Side Effects: Systemic side effects to corticosteroids are generally dependent on dose and duration of treatment. Short-term use of prednisone is unlikely to cause adverse effects. Adverse effects are more common in animals on immunosuppressive doses.nbsp; Side effects seen in dogs include polyuria, polydipsia, polyphagia, poor haircoat, GI disturbance, diarrhea, vomiting, weight gain, GI ulceration, pancreatitis, lipidemia, elevated liver enzymes, diabetes mellitus, muscle wasting, and possible behavioral changes.nbsp; Polyuria, polydipsia, polyphagia may be seen in dogs even on short-term therapy.nbsp; Although cats are less likely to develop side effects than dogs, occasionally polyuria, polydipsia, polyphagia, weight gain, GI disturbances and behavioral changes occur.nbsp; Corticosteroids can cause or worsen gastric ulcers. Precautions: nbsp; Chronic or inappropriate use of corticosteroids can cause life threatening hormonal and metabolic changes.nbsp; Adverse effects due to corticosteroid treatment usually occur with long-term administration of the drug, especially when h

Isoxsuprine 20 mg, 1000 tablets Isoxsuprine is a vasodilator used widely in horses for nonspecific lameness, navicular disease and laminitis. Isoxsuprine is a synthetic chemical with epinephrine-Like effects. Its action relates specifically to the walls of arteries which are located in the muscles, internal organs, and extremities. Isoxsuprine causes these arteries to dilate. INDICATIONS Isoxsuprine has been used in the treatment of navicular disease and laminitis, where it is presumed that the disease is associated with some degree of decreased blood supply. Isoxsuprine also has been used to relax the uterus during the treatment of uterine infections. In other species, it has been suggested that isoxsuprine can be used to attempt to treat premature labor. DOSAGE AND ROUTE Of ADMINISTRATION Isoxsuprine is given orally in a dose ranging from 0.2 mg/kg to 0.6 mg/kg, depending on the treating veterinarian's discretion. This dose is given 2-4 times daily. SIDE EFFECTS/TOXICITY The major side effects concern the cardiovascular system. Isoxsuprine causes the systolic blood pressure (e.g., 150/100, the upper number, 150 being systolic) to rise, while the diastolic pressure falls. Reported side effects in other species include nervousness, trembling, weakness, dizziness, palpitations, nausea, and vomiting. If the horse appears to be developing side effects, consult the veterinarian regarding advisability of stopping this medication, or changing dosage. DRUG INTERACTIONS If a horse is receiving isoxsuprine therapy, the veterinarian must know this before treatment occurs with any anesthetic, tranquilizer, or narcotic drug. PREGNANCY/NURSING No information is available concerning safety of isoxsuprine use during pregnancy'. Isoxsuprine is known to cause relaxation of the uterus. DRUG TESTING ARCI: Isoxsuprine is a Class 4 drug in the ARCI uniform classification system.

TRANQULEX TEA PILL(DING XIN) Functions and indications: Tonifies qi, nourishes blood and yin calms shen, disperses internal heat. Use to restlessness, anxiety, insomnia, palpitations and poor memory. Ingredients: Duhuo root, Eucommia bark, Loranthus stem, Relative root, Tuckahoe root, Foxglove root, Ginger root, Cinnamon bark, Tangkwei root, Licorice root Directions: As a dietary supplement, take 9 pills 2 times. Store in cool and dry place. Warning: Do not use if you are pregnant. Content: 100 pills (250mg each) This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Lysodren 500 mg, 100 Tablets Lysodren (Mitotane) is used to treat pituitary- dependent hyperadrenocortic ism (Cushing's Disease) and adrenal tumors). Lysodren Miotane Prescriber Highlights - Adrenal cytoxic agent used for medical treatment of pituitary- dependent hy- peradrencorticism Caution: pregnancy, diabetes, and preexisting renal or hepatic disease Adverse Effects: Lethargy, ataxia, wekness, anorexia, vomiting, and/or diarrhea; liver changes possible. Relapses are not uncommon All dogs receiving mitotane therapy should receive additional glucocorticoid supplementation if undergoing a stress (e.g., surgery, trauma, acute illness) Monitoring is mandatorty Avoid human exposure Drug interactions Chemistry Mitotane, also commonly known in veterinary medicine as DDD, is structuarally related to the infamous insecticide, chlorophenothane (DDT). It occurs as a white, crystalline powder with slightly aromatic odor. It is practically insoluble in water and soluble in alcohol. Pharmacology While mitotane is considered an adrenal cytotoxic agent, it apparently can also inhibit adrenocortical function without causing cell destruction. the exact mechan- nisms of action for these are not clearly understood. In dogs with pituitary- dependent hyperadrenocortic ism (PDH), mitotane has been dem- onstrated to cause severe, progressive necrosis of the zona fasciculata and zona reticularis . These effects occur quite rapidly (usually within 5-10 days of starting therapy). It has been stated that mitotane spares the zona glomerulosa and therefore aldosterone synthesis is un- affected. This is only partially true, as the zona glomerulosa may also be affected by mi- totane therapy, but it is uncommon for clinically significant effects on aldosterone produc- tion to be noted with therapy. Uses/Indications Inveterinary medicine, mitotane is used primarily for the medical treatment of pituitary- dependent hyperadrenocortic ism (PDH), principally in the dog. It has also been used for the palliative treatment of adrenal carcinorma in humans and dogs. Contraindications /Precautions Mitotane is contraindicated in patients known to be hy- persensitive to it. Patients with concurrent diabetes mellitus may have rapidly changing insulin requirements during the initial treatment period. these animals should be closely monitored until they are clinically stable. Dogs with preexisting renal or hepatic disease should receive the drug with caution and with more intense monitoring. some clinicians recommend giving prednisolone at 0.2 mg/kg/day during the initial treatment period (0.4 mg/kg/day to diabetic dogs) to reduce the potential for side effects from acute endogenous steroid withdrawal. Other clinicians have argued that routinely administering steroids masks the clinical markers that signify when the endpoint of ther- apy has been reached and must be withdrawn 2-3 days before ACTH stimulation tests can be done. Since in adequately observed patients, adverse effects requiring glucocor

Methylprednisolon e 4 mg, 100 Tablets Anti- inflammatory medication indicated for a number of dermal, allergic, ocular, otic and musculoskeletal conditions. Methylprednisolon e 4mg, 100 Tablets Product Description: The indications for Methylprednisolon e Tablets are the same as those for other anti- inflammatory steroids and comprise the various collagen, dermal, allergic, ocular, Otic, and musculoskeletal conditions known to be responsive to the anti- inflammatory corticosteroids. Representative of the conditions in which the use of steroid therapy and the benefits to be derived there from have had repeated confirmation in the veterinary literature are: (1) dermal conditions, such as non-specific eczema, summer dermatitis, and burns; (2) allergic manifestations, such as acute urticaria, allergic dermatitis, drug and serum reactions, bronchial asthma, and pollen sensitivities; (3) ocular conditions, such as iritis, iridocyclitis, secondary glaucoma, uveitis, and chorioretinitis; (4) Otic conditions, such as otitis externa; (5) musculoskeletal conditions, such as myositis, rheumatoid arthritis, osteoarthritis, and bursitis; (6) various chronic or recurrent diseases of unknown etiology such as ulcerative colitis and nephrosis. In acute adrenal insufficiency, Methylprednisolon e may be effective because of its ability to correct the defect in carbohydrate metabolism and relieve the impaired diuretic response to water characteristic of primary or secondary adrenal insufficiency. However, because this agent lacks significant mineral corticoid activity, the parent hormones, Solu-Cortef containing hydrocortisone sodium succinate, Cortef containing hydrocortisone, or cortisone should be used when salt retention is indicated. Pharmacology: Methylprednisolon e, a potent anti- inflammatory steroid synthesized and developed in the Research Laboratories of The Upjohn Company is the 6-methyl derivative of prednisolone. It has a greater anti- inflammatory potency than prednisolone and even less tendency than prednisolone to induce sodium and water retention. Its advantage over the older corticoids lies in its ability to achieve equal anti- inflammatory effect with lower dose, while at the same time enhancing the split between anti- inflammatory and mineral corticoid activities. Dosage and Administration: For oral use in dogs and cats. Dosage: Average total daily oral doses for dogs and cats are as follows: 5 to 15 lb body wt 2 mg 15 to 40 lb body wt 2 to 4 mg 40 to 80 lb body wt 4 to 8 mg The total daily dose should be given in divided doses, 6 to 10 hours apart. Administration: The keystone of satisfactory therapeutic management with Methylprednisolon e Tablets, as with its steroid predecessors, is individualization of dosage in reference to the severity of the disease, the anticipated duration of steroid therapy, and the animal patient's threshold or tolerance for steroid excess. The prime objective of steroid therapy should be to achieve a satisfactory degree of control

Fish Zole (Metronidazole) 250 mg, 30 Tablets Fish Zole is useful in the control of "Hole-in-the-Head" and "Angle Problems" in Cichlid and Discus. For ornamental and aquarium fish only. Metronidazole Trade and Other Names Flagyl; many brands available Drug Class Antibacterial, antiparasitic, antiprotozoal Mechanism of Action and Clinical Use Disrupts DNA in organism via reaction with intracellular metabolite. Action is specific for anaerobic bacteria and protozoa. Resistance is rare. Active against some protozoa, including Giardia organisms; however, other drugs such as fenbendazole have been used for Giardia infection. Adverse Effects Most severe adverse effect is dose-related CNS toxicity. High doses have caused lethargy, CNS depression, ataxia, vomiting, and weakness. Metronidazole may be mutagenic. Contraindications , Precautions, and Drug Interactions Fetal abnormalities have not been demostrated in animals with recommended doses, but use with caution during pregnancy. Instructions for Use Metronidazole is one of the most commonly used drugs for anaerobic infections. It is effective for giardiasis; other drugs used for Giardia infection include albendazole, fenbendazole, and quinacrine. Maximum dose that should be administered is 50-65 mg/kg,q24h, in any species. Tablets have been broken or crushed for oral administration to cats; however, cats find these unpalatable. Small Animal Dosage Information Anaerobic Infection: Dogs: 15 mg/kg,q12h, PO; or 12 mg/kg, q8h, PO. Cats: 10-25 mg/kg, q24h, PO. Giardia Infection: Dogs: 12-15 mg/kg,q12h, PO, x 8 days. Cats: 17 mg/kg (1/3 tablet/cat), q24h, PO, x 8 days

Diphenhydramine 25 mg, 1000 Tablets Diphenhydramine is an antihistamine used in the treatment of allergies, insect bites or stings and other causes of itching. It is also used for its sedative and antiemetic effects in the treatment of motion sickness and travel anxiety. New Page 2 Diphenhydramine 25mg, 1000 Tablets Product Description: Diphenhydramine is an antihistamine used in the treatment of allergies, insect bites or stings and other causes of itching. It is also used for its sedative and antiemetic effects in the treatment of motion sickness and travel anxiety. It is also used for its antitussive effect. Availability : Diphenhydramine is a non-prescription (OTC) product available as 25mg and 50mg tablets or capsules as well. How this medicine should be used : Diphenhydramine is FDA approved for external use in dogs and cats. Diphenhydramine oral and injectable is not FDA approved for use in veterinary medicine; however, it is a commonly accepted practice to use this medication in dogs and cats. The usual dose in dogs and cats is 0.5-2mg/pound every 8-12 hours. The slow release capsule should not be mixed or dissolved in food. Do not use diphenhydramine found in combination products containing sinus or cold medicine. What are the side effects : Side effects of diphenhydramine include drowsiness, dry mouth and urinary retention. Rarely, vomiting and diarrhea can occur. What special precautions are there : Do not use this medication in animals that are allergic to it or other antihistamines. Do not use in animals with glaucoma, prostate disease, urinary obstruction, and high blood pressure. Do not use in pregnant or nursing animals. Use with caution when given with other CNS depressant drugs such as tranquilizers or barbiturates. Always tell your veterinarian and pharmacist what other medications your pet is taking. In the event of an overdose : Contact your veterinarian or veterinary emergency room. Symptoms of overdose can include seizures, extreme drowsiness, coma, respiratory depression and death. How should I store this medication : Keep this medication in the container it came in, tightly closed. Store this medication at room temperature, away from excess heat, light and moisture. Do not store in the bathroom. Throw away any medication that is outdated or no longer needed. Keep medication away from children and pets. This information sheet is for educational purposes only and is intended to be a supplement to, and not a substitute for, the expertise and professional judgment of your veterinarian. The information is NOT to be used for diagnosis or treatment of your pet. You should always consult your own veterinarian for specific advice concerning the treatment of your pet. nbsp; The information is not intended to cover all possible uses, directions, precautions, warnings, allergic reactions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for yo

Cimetidine 400 mg, 100 Tablets Cimetidine is used in the treatment and prevention of stomach and intestinal ulcers in dogs, cats, horses and other animals. Cimetidine | Cimetidine HCl Cimetidine has been used for the treatment and/or prophylaxis of gastric, abomasal and duodenal ulcers, uremic gastritis, stress-related or drug-induced erosive gastritis, esophagitis, duodenal gastric reflux and esophageal reflux. It has also been employed to treat hypersecretory conditions associated with gastrinomas and systemic mastocytosis. Cimetidine has also been used investigationally as a immunomodulating agent (see doses) in dogs. Prototype histamine-2 blocker used to reduce GI acid production Contraindications : hypersensitivity. Caution: geriatric patients, hepatic or renal insufficiency Storage/Stability /Compatibility Cimetidine products should be stored protected from light and kept at room temperature. Do not refrigerate the injectable product as precipitation may occur. Oral dosage forms should be stored in tight containers. The cimetidine injectable product is compatible with the commonly used IV infusions solutions, including amino acid (TPN) solutions, but should be used within 48 hours of dilution. Cimetidine is also reported to be compatible with the following drugs: acetazolamide sodium, amikacin sulfate, atropine sulfate, carbenicillin disodium, cefoxitin sodium, chlorothiazide sodium, clindamycin phosphate, colistimethate sodium, dexamethasone sodium phosphate, digoxin, epinephrine, erythromycin lactobionate, furosemide, gentamicin sulfate, heparin sodium, insulin (regular), isoproterenol HCl, lidocaine HCl, lincomycin HCl, methylprednisolon e sodium succinate, nafcillin sodium, norepinephrine bitartrate, penicillin G potassium/sodium, phytonadione, polymyxin B sulfate, potassium chloride, protamine sulfate, quinidine gluconate, sodium nitroprusside, tetracycline HCl, vancomycin HCl, verapamil HCl, and vitamin B complex (w/ or w/o C). The following drugs are reported to be either incompatible with cimetidine or data are conflicting: amphotericin B, ampicillin sodium, cefamandole naftate, cefazolin sodium, cephalothin sodium, and pentobarbital sodium. Compatibility is dependent upon factors such as pH, concentration, temperature and diluents used. Pharmacology At the H 2 receptors of the parietal cells, cimetidine competitively inhibits histamine, thereby reducing gastric acid output both during basal conditions and when stimulated by food, pentagastrin, histamine or insulin. Gastric emptying time, pancreatic or biliary secretion, and lower esophageal pressures are not altered by cimetidine. By decreasing the amount of gastric juice produced, cimetidine also decreases the amount of pepsin secreted. Cimetidine has an apparent immunomodulating effect as it has been demonstrated to reverse suppressor T cell-mediated immune suppression. It also possesses weak anti-androgenic activity. Pharmacokinetics Pharmacokinetic data for veterinary species is l

Cimetidine 800 mg, 100 Tablets Cimetidine is used in the treatment and prevention of stomach and intestinal ulcers in dogs, cats, horses and other animals. Cimetidine | Cimetidine HCl Cimetidine has been used for the treatment and/or prophylaxis of gastric, abomasal and duodenal ulcers, uremic gastritis, stress-related or drug-induced erosive gastritis, esophagitis, duodenal gastric reflux and esophageal reflux. It has also been employed to treat hypersecretory conditions associated with gastrinomas and systemic mastocytosis. Cimetidine has also been used investigationally as a immunomodulating agent (see doses) in dogs. Prototype histamine-2 blocker used to reduce GI acid production Contraindications : hypersensitivity. Caution: geriatric patients, hepatic or renal insufficiency Storage/Stability /Compatibility Cimetidine products should be stored protected from light and kept at room temperature. Do not refrigerate the injectable product as precipitation may occur. Oral dosage forms should be stored in tight containers. The cimetidine injectable product is compatible with the commonly used IV infusions solutions, including amino acid (TPN) solutions, but should be used within 48 hours of dilution. Cimetidine is also reported to be compatible with the following drugs: acetazolamide sodium, amikacin sulfate, atropine sulfate, carbenicillin disodium, cefoxitin sodium, chlorothiazide sodium, clindamycin phosphate, colistimethate sodium, dexamethasone sodium phosphate, digoxin, epinephrine, erythromycin lactobionate, furosemide, gentamicin sulfate, heparin sodium, insulin (regular), isoproterenol HCl, lidocaine HCl, lincomycin HCl, methylprednisolon e sodium succinate, nafcillin sodium, norepinephrine bitartrate, penicillin G potassium/sodium, phytonadione, polymyxin B sulfate, potassium chloride, protamine sulfate, quinidine gluconate, sodium nitroprusside, tetracycline HCl, vancomycin HCl, verapamil HCl, and vitamin B complex (w/ or w/o C). The following drugs are reported to be either incompatible with cimetidine or data are conflicting: amphotericin B, ampicillin sodium, cefamandole naftate, cefazolin sodium, cephalothin sodium, and pentobarbital sodium. Compatibility is dependent upon factors such as pH, concentration, temperature and diluents used. Pharmacology At the H 2 receptors of the parietal cells, cimetidine competitively inhibits histamine, thereby reducing gastric acid output both during basal conditions and when stimulated by food, pentagastrin, histamine or insulin. Gastric emptying time, pancreatic or biliary secretion, and lower esophageal pressures are not altered by cimetidine. By decreasing the amount of gastric juice produced, cimetidine also decreases the amount of pepsin secreted. Cimetidine has an apparent immunomodulating effect as it has been demonstrated to reverse suppressor T cell-mediated immune suppression. It also possesses weak anti-androgenic activity. Pharmacokinetics Pharmacokinetic data for veterinary species is l

Cimetidine 400 mg, 500 Tablets Cimetidine is used in the treatment and prevention of stomach and intestinal ulcers in dogs, cats, horses and other animals. Cimetidine | Cimetidine HCl Cimetidine has been used for the treatment and/or prophylaxis of gastric, abomasal and duodenal ulcers, uremic gastritis, stress-related or drug-induced erosive gastritis, esophagitis, duodenal gastric reflux and esophageal reflux. It has also been employed to treat hypersecretory conditions associated with gastrinomas and systemic mastocytosis. Cimetidine has also been used investigationally as a immunomodulating agent (see doses) in dogs. Prototype histamine-2 blocker used to reduce GI acid production Contraindications : hypersensitivity. Caution: geriatric patients, hepatic or renal insufficiency Storage/Stability /Compatibility Cimetidine products should be stored protected from light and kept at room temperature. Do not refrigerate the injectable product as precipitation may occur. Oral dosage forms should be stored in tight containers. The cimetidine injectable product is compatible with the commonly used IV infusions solutions, including amino acid (TPN) solutions, but should be used within 48 hours of dilution. Cimetidine is also reported to be compatible with the following drugs: acetazolamide sodium, amikacin sulfate, atropine sulfate, carbenicillin disodium, cefoxitin sodium, chlorothiazide sodium, clindamycin phosphate, colistimethate sodium, dexamethasone sodium phosphate, digoxin, epinephrine, erythromycin lactobionate, furosemide, gentamicin sulfate, heparin sodium, insulin (regular), isoproterenol HCl, lidocaine HCl, lincomycin HCl, methylprednisolon e sodium succinate, nafcillin sodium, norepinephrine bitartrate, penicillin G potassium/sodium, phytonadione, polymyxin B sulfate, potassium chloride, protamine sulfate, quinidine gluconate, sodium nitroprusside, tetracycline HCl, vancomycin HCl, verapamil HCl, and vitamin B complex (w/ or w/o C). The following drugs are reported to be either incompatible with cimetidine or data are conflicting: amphotericin B, ampicillin sodium, cefamandole naftate, cefazolin sodium, cephalothin sodium, and pentobarbital sodium. Compatibility is dependent upon factors such as pH, concentration, temperature and diluents used. Pharmacology At the H 2 receptors of the parietal cells, cimetidine competitively inhibits histamine, thereby reducing gastric acid output both during basal conditions and when stimulated by food, pentagastrin, histamine or insulin. Gastric emptying time, pancreatic or biliary secretion, and lower esophageal pressures are not altered by cimetidine. By decreasing the amount of gastric juice produced, cimetidine also decreases the amount of pepsin secreted. Cimetidine has an apparent immunomodulating effect as it has been demonstrated to reverse suppressor T cell-mediated immune suppression. It also possesses weak anti-androgenic activity. Pharmacokinetics Pharmacokinetic data for veterinary species is l

Hydroxyzine HCl 10 mg, 100 Tablets The generic of Atarax and used for the relief of allergies, including the itching and chewing of allergic dermatitis. Hydroxyzine (generic for Atarax) is used by veterinarians for the treatment of allergies in dogs. It is available as 10mg, 25mg and 50mg tablets. The usual dose for dogs is 1mg/pound by mouth every 6 to 8 hours. It should not be used in pregnant or nursing animals.

Hydroxyzine HCl 50 mg, 1000 Tablets The generic of Atarax and used for the relief of allergies, including the itching and chewing of allergic dermatitis. Hydroxyzine (generic for Atarax) is used by veterinarians for the treatment of allergies in dogs. It is available as 10mg, 25mg and 50mg tablets. The usual dose for dogs is 1mg/pound by mouth every 6 to 8 hours. It should not be used in pregnant or nursing animals.

Hydroxyzine HCl 25 mg, 100 Tablets The generic of Atarax and used for the relief of allergies, including the itching and chewing of allergic dermatitis. Hydroxyzine (generic for Atarax) is used by veterinarians for the treatment of allergies in dogs. It is available as 10mg, 25mg and 50mg tablets. The usual dose for dogs is 1mg/pound by mouth every 6 to 8 hours. It should not be used in pregnant or nursing animals.

Hydroxyzine HCl 50 mg, 100 Tablets The generic of Atarax and used for the relief of allergies, including the itching and chewing of allergic dermatitis. Hydroxyzine (generic for Atarax) is used by veterinarians for the treatment of allergies in dogs. It is available as 10mg, 25mg and 50mg tablets. The usual dose for dogs is 1mg/pound by mouth every 6 to 8 hours. It should not be used in pregnant or nursing animals.

Glipizide 5 mg, 100 Tablets Glipizide is a prescription medication used to lower the blood sugar level in diabetic animals. Glipizide (Glucotrol) Product Description: Glipizide is used to lower the blood sugar level in diabetic cats. Dose and Administration: Always follow the dosage instructions provided by your veterinarian. Glipizide should be given with meals, as directed by your veterinarian. This medication should be given only to the pet for whom it was prescribed. Possible Side Effects: Some possible side effects may include vomiting, sudden lowering of the blood sugar, weakness, wobbling, inability to stand, extreme hunger, shivering, lethargy, shaking, seizures, or coma. If you see these signs contact your veterinarian immediately. May cause toxic effects in the liver. Signs would include vomiting, depression, loss of appetite, and jaundice (yellowing of thegums, skin, or eyes). Contact your veterinarian immediately if you see these signs. Uncommon side effects include suppression of the bone marrow. This may lead to anemia, with pale gums, weakness, and lethargy; bruising or bleeding tendencies; and decreased white blood cell counts, which may cause the animal to be more at risk of infections. If your pet experiences an allergic reaction to the medication, signs may include facial swelling, hives, scratching, sudden onset of diarrhea, vomiting, shock, seizures, pale gums, cold limbs, or coma. If you notice any of these signs, contact your veterinarian immediately. Precautions: Not for use in animals allergic to glipizide or sulfa drugs. Do not use in pregnant or lactating animals . Do not use in animals with untreated diseases of the adrenal or pituitary glands or those with liver, kidney, or thyroid disease. Glipizide is not effective in treating cats with complications of diabetes such as diabetic coma, acidosis, ketosis, or insulin resistance. Contact your veterinarian if you notice an increase in drinking or urinating. Drug Interactions: Always inform your veterinarian of what medications your pet is currently taking before administering a new medication. Caution: Keep this and all other medications out of the reach of children and pets . People who are allergic to sulfa drugs should wear gloves and use extreme caution when handling this medication. Storage: Refrigerate oral suspension. Store other forms at room temperature in a tight, light resistant, childproof container.