Cyclizine: A histamine H1 antagonist given by mouth or parenterally for the control of postoperative and drug-induced vomiting and in motion sickness. (From Martindale, The Extra Pharmacopoeia, 30th ed, p935)Triprolidine: Histamine H1 antagonist used in allergic rhinitis; ASTHMA; and URTICARIA. It is a component of COUGH and COLD medicines. It may cause drowsiness.Perphenazine: An antipsychotic phenothiazine derivative with actions and uses similar to those of CHLORPROMAZINE.Antiemetics: Drugs used to prevent NAUSEA or VOMITING.Histamine H1 Antagonists: Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood.Postoperative Nausea and Vomiting: Emesis and queasiness occurring after anesthesia.Meclizine: A histamine H1 antagonist used in the treatment of motion sickness, vertigo, and nausea during pregnancy and radiation sickness.Copyright: It is a form of protection provided by law. In the United States this protection is granted to authors of original works of authorship, including literary, dramatic, musical, artistic, and certain other intellectual works. This protection is available to both published and unpublished works. (from Circular of the United States Copyright Office, 6/30/2008)Administration, Oral: The giving of drugs, chemicals, or other substances by mouth.Motion Sickness: Disorder caused by motion, as sea sickness, train sickness, car sickness, air sickness, or SPACE MOTION SICKNESS. It may include nausea, vomiting and dizziness.Histamine H1 Antagonists, Non-Sedating: A class of non-sedating drugs that bind to but do not activate histamine receptors (DRUG INVERSE AGONISM), thereby blocking the actions of histamine or histamine agonists. These antihistamines represent a heterogenous group of compounds with differing chemical structures, adverse effects, distribution, and metabolism. Compared to the early (first generation) antihistamines, these non-sedating antihistamines have greater receptor specificity, lower penetration of BLOOD-BRAIN BARRIER, and are less likely to cause drowsiness or psychomotor impairment.PiperazinesLoratadine: A second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (HISTAMINE H1 ANTAGONISTS) it lacks central nervous system depressing effects such as drowsiness.Cetirizine: A potent second-generation histamine H1 antagonist that is effective in the treatment of allergic rhinitis, chronic urticaria, and pollen-induced asthma. Unlike many traditional antihistamines, it does not cause drowsiness or anticholinergic side effects.Urticaria: A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress.Newcastle disease virus: The most well known avian paramyxovirus in the genus AVULAVIRUS and the cause of a highly infectious pneumoencephalitis in fowl. It is also reported to cause CONJUNCTIVITIS in humans. Transmission is by droplet inhalation or ingestion of contaminated water or food.Newcastle Disease: An acute febrile, contagious, viral disease of birds caused by an AVULAVIRUS called NEWCASTLE DISEASE VIRUS. It is characterized by respiratory and nervous symptoms in fowl and is transmissible to man causing a severe, but transient conjunctivitis.Paralysis: A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45)Emetics: Agents that cause vomiting. They may act directly on the gastrointestinal tract, bringing about emesis through local irritant effects, or indirectly, through their effects on the chemoreceptor trigger zone in the postremal area near the medulla.Cholinergic Antagonists: Drugs that bind to but do not activate CHOLINERGIC RECEPTORS, thereby blocking the actions of ACETYLCHOLINE or cholinergic agonists.Vestibule, Labyrinth: An oval, bony chamber of the inner ear, part of the bony labyrinth. It is continuous with bony COCHLEA anteriorly, and SEMICIRCULAR CANALS posteriorly. The vestibule contains two communicating sacs (utricle and saccule) of the balancing apparatus. The oval window on its lateral wall is occupied by the base of the STAPES of the MIDDLE EAR.Biological Science Disciplines: All of the divisions of the natural sciences dealing with the various aspects of the phenomena of life and vital processes. The concept includes anatomy and physiology, biochemistry and biophysics, and the biology of animals, plants, and microorganisms. It should be differentiated from BIOLOGY, one of its subdivisions, concerned specifically with the origin and life processes of living organisms.Receptors, Histamine: Cell-surface proteins that bind histamine and trigger intracellular changes influencing the behavior of cells. Histamine receptors are widespread in the central nervous system and in peripheral tissues. Three types have been recognized and designated H1, H2, and H3. They differ in pharmacology, distribution, and mode of action.Dictionaries, ChemicalAgrochemicals: Chemicals used in agriculture. These include pesticides, fumigants, fertilizers, plant hormones, steroids, antibiotics, mycotoxins, etc.Dictionaries, MedicalDictionaries as Topic: Lists of words, usually in alphabetical order, giving information about form, pronunciation, etymology, grammar, and meaning.Biopharmaceutics: The study of the physical and chemical properties of a drug and its dosage form as related to the onset, duration, and intensity of its action.Scopolamine Hydrobromide: An alkaloid from SOLANACEAE, especially DATURA and SCOPOLIA. Scopolamine and its quaternary derivatives act as antimuscarinics like ATROPINE, but may have more central nervous system effects. Among the many uses are as an anesthetic premedication, in URINARY INCONTINENCE, in MOTION SICKNESS, as an antispasmodic, and as a mydriatic and cycloplegic.Xylitol: A five-carbon sugar alcohol derived from XYLOSE by reduction of the carbonyl group. It is as sweet as sucrose and used as a noncariogenic sweetener.Patents as Topic: Exclusive legal rights or privileges applied to inventions, plants, etc.Biofuels: Hydrocarbon-rich byproducts from the non-fossilized BIOMASS that are combusted to generate energy as opposed to fossilized hydrocarbon deposits (FOSSIL FUELS).Body Composition: The relative amounts of various components in the body, such as percentage of body fat.Tablets: Solid dosage forms, of varying weight, size, and shape, which may be molded or compressed, and which contain a medicinal substance in pure or diluted form. (Dorland, 28th ed)Excipients: Usually inert substances added to a prescription in order to provide suitable consistency to the dosage form. These include binders, matrix, base or diluent in pills, tablets, creams, salves, etc.Foramen Ovale, Patent: A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance.Drug Information Services: Services providing pharmaceutic and therapeutic drug information and consultation.Pamphlets: Printed publications usually having a format with no binding and no cover and having fewer than some set number of pages. They are often devoted to a single subject.Drug Labeling: Use of written, printed, or graphic materials upon or accompanying a drug container or wrapper. It includes contents, indications, effects, dosages, routes, methods, frequency and duration of administration, warnings, hazards, contraindications, side effects, precautions, and other relevant information.Patient Education as Topic: The teaching or training of patients concerning their own health needs.Formularies as Topic: Works about lists of drugs or collections of recipes, formulas, and prescriptions for the compounding of medicinal preparations. Formularies differ from PHARMACOPOEIAS in that they are less complete, lacking full descriptions of the drugs, their formulations, analytic composition, chemical properties, etc. In hospitals, formularies list all drugs commonly stocked in the hospital pharmacy.Drug Industry: That segment of commercial enterprise devoted to the design, development, and manufacture of chemical products for use in the diagnosis and treatment of disease, disability, or other dysfunction, or to improve function.Medical Records Systems, Computerized: Computer-based systems for input, storage, display, retrieval, and printing of information contained in a patient's medical record.Coproporphyria, Hereditary: An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.Coproporphyrins: Porphyrins with four methyl and four propionic acid side chains attached to the pyrrole rings. Elevated levels of Coproporphyrin III in the urine and feces are major findings in patients with HEREDITARY COPROPORPHYRIA.Coproporphyrinogen Oxidase: An enzyme that catalyzes the oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX by the conversion of two propionate groups to two vinyl groups. It is the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME, and is encoded by CPO gene. Mutations of CPO gene result in HEREDITARY COPROPORPHYRIA.Porphyrias, Hepatic: A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues.Porphyrias: A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues.Porphyrins: A group of compounds containing the porphin structure, four pyrrole rings connected by methine bridges in a cyclic configuration to which a variety of side chains are attached. The nature of the side chain is indicated by a prefix, as uroporphyrin, hematoporphyrin, etc. The porphyrins, in combination with iron, form the heme component in biologically significant compounds such as hemoglobin and myoglobin.Porphyrinogens: Colorless reduced precursors of porphyrins in which the pyrrole rings are linked by methylene (-CH2-) bridges.QuinuclidinesNausea: An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses.Serotonin 5-HT3 Receptor Antagonists: Drugs that bind to but do not activate SEROTONIN 5-HT3 RECEPTORS, thereby blocking the actions of SEROTONIN or SEROTONIN 5-HT3 RECEPTOR AGONISTS.Vomiting: The forcible expulsion of the contents of the STOMACH through the MOUTH.Isoquinolines: A group of compounds with the heterocyclic ring structure of benzo(c)pyridine. The ring structure is characteristic of the group of opium alkaloids such as papaverine. (From Stedman, 25th ed)Ondansetron: A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.

Comparison of ondansetron and cyclizine for prevention of nausea and vomiting after day-case gynaecological laparoscopy. (1/14)

We have compared ondansetron 4 mg i.v. and cyclizine 50 mg i.v., in a double-blind, randomized, placebo-controlled study for the prevention of postoperative nausea and vomiting (PONV) for 24 h after day-case gynaecological laparoscopy. Compared with placebo (n = 58), ondansetron (n = 60) and cyclizine (n = 57) reduced significantly the incidence of moderate or severe nausea (30% and 23% vs 52%; P = 0.02 and P = 0.001, respectively) and requirement for escape antiemetic (28% and 16% vs 47%; P = 0.04 and P < 0.001, respectively) before discharge from hospital. There were no significant differences in PONV after discharge. Significantly more patients suffered no PONV before and after discharge after ondansetron and cyclizine compared with placebo (31% and 33% vs 12%; P = 0.02 and P < 0.01, respectively). For diagnostic laparoscopy (n = 74), fewer patients received escape antiemetic after cyclizine than after ondansetron (4% vs 37%; P < 0.01); for laparoscopic sterilization (n = 101), both antiemetics were equally effective. Ondansetron and cyclizine both reduced severe and moderate nausea and the need for antiemetic therapy after day-case gynaecological laparoscopy.  (+info)

Chronic ergot toxicity: A rare cause of lower extremity ischemia. (2/14)

Chronic ergot toxicity is a rare cause of lower extremity ischemia. The cornerstone of therapy in ergot toxicity is to discontinue the use of caffeine, cigarettes, and all ergot-containing medications. Although multiple different therapies have been recommended for acute toxicity, no specific treatment is uniformly recommended in chronic toxicity. We present a case of long-term ergot use for migraine headaches in a woman who had severe chronic lower extremity claudication. This case demonstrates the unique features associated with the diagnosis and management of chronic ergot toxicity. We recommend a conservative approach consisting of observation, antiplatelet agents, and the discontinuance of ergots. If symptoms progress to rest pain or gangrene, surgical treatment should be considered.  (+info)

Randomized, placebo-controlled trial of combination antiemetic prophylaxis for day-case gynaecological laparoscopic surgery. (3/14)

In a randomized, double-blind trial, we compared i.v. ondansetron 4 mg (control), i.v. ondansetron 4 mg and cyclizine 50 mg (combination) and i.v. saline 0.9% (placebo), given after induction of standardized anaesthesia, for the prevention of nausea and vomiting (PONV) after day-case gynaecological laparoscopic surgery. Compared with placebo, fewer patients in the control group vomited (9/20 versus 11/59, P = 0.02) or needed rescue antiemetic (7/20 versus 9/59, P = 0.06) before discharge. Compared with the control, fewer patients in the combination group (n = 60) vomited (11/59 versus 2/60, P = 0.01) or needed rescue antiemetic (29/59 versus 2/60, P = 0.03) before discharge. The incidence of vomiting in the combination group was less than 5% overall. Compared with the control, the combination group had a significantly lower incidence (P = 0.001) and severity (P < 0.001) of nausea after discharge and more patients with no PONV at any time during the study (15/59 versus 27/60, P = 0.03). Unlike the placebo and control groups, no patient receiving combination prophylaxis was admitted overnight for PONV management.  (+info)

Standard treatment: the role of antihistamines. (4/14)

Histamine-1 (H1) antihistamines are the first-line drug for the treatment of urticaria. Major progress has been achieved in recent years both in the understanding of their ligands, the H1-histamine receptors, and therefore in the mechanisms of their pharmacologic effects, as well as in the development of safer antihistamines with low or no sedating effects and no interactions on the level of potassium channels leading to QT-prolongations and interactions on the level of cytochrome P450 isoenzymes. This development has brought antihistamines very close to the ideal antihistamines that are desired by clinicians to treat most types of urticaria in patients who have to take these drugs for a long time.  (+info)

A comparison of the efficacy of cyclizine and perhenazine in reducing the emetic effects of morphine and pethidine. (5/14)

1 The ability of cyclizine (50 mg) and perphenazine (2.5 and 5.0 mg) to counteract the emetic effects of pethidine (100 mg) and morphine (10 and 15 mg) was compared in women undergoing a standard minor operation with a standard anaesthetic. 2 Perphenazine (5.0 mg) was as effective an anti-emetic as cyclizine (50 mg) and both were more effective than perphenazine (2.5 mg). 3 The reduction in vomiting and nausea by cyclizine (50 mg) and perphenazine (5 mg) was approximately the same following pethidine (100 mg) and morphine (10 mg) but much less against the larger dose of morphine. 4 Both anti-emetics had a rapid onset of action but their anti-emetic activity did not last as long as the emetic effect of morphine. 5 Perphenazine (5 mg) was accompanied by an unacceptably high incidence of restlessness. 6 In clinical practice cyclizine (50 mg) is preferred to perphenazine (5 mg) as an anti-emetic.  (+info)

Prevention of postoperative nausea and vomiting after spinal morphine for Caesarean section: comparison of cyclizine, dexamethasone and placebo. (6/14)

BACKGROUND: Low-dose intrathecal (spinal) morphine (0.1-0.2 mg) for Caesarean section delivers excellent postoperative analgesia but is associated with significant nausea and vomiting. We compared the antiemetic efficacy of cyclizine, dexamethasone, and placebo in this clinical setting. METHODS: Ninety-nine women undergoing elective Caesarean section under spinal anaesthesia were allocated randomly, in a double-blind study design, to receive either cyclizine 50 mg, dexamethasone 8 mg, or placebo as a single-dose infusion in saline 0.9%, 100 ml on completion of surgery. Spinal anaesthesia consisted of: hyperbaric bupivacaine 0.5%, 2.0 ml; fentanyl 10 micro g; and spinal morphine 0.2 mg. The primary outcome measure was the incidence of nausea. RESULTS: The incidence of nausea was significantly less in patients receiving cyclizine compared with dexamethasone and placebo (33 vs 60 and 67%, respectively, P<0.05). Severity of nausea and number of vomiting episodes were also less at 3-6 h in cyclizine patients. Overall satisfaction with postoperative care at 24 h, expressed on a 100 mm visual analogue scale, was greater in cyclizine [78 (28)] than either dexamethasone [58 (31), P=0.03] or placebo [51 (28), P=0.008]. CONCLUSION: We conclude that following spinal morphine 0.2 mg and fentanyl 10 micro g analgesia for Caesarean section, cyclizine 50 mg i.v. reduces the incidence of nausea compared with dexamethasone 8 mg i.v. or placebo. It also lessens the severity of nausea and vomiting, and increases maternal satisfaction in the early postoperative period.  (+info)

Best evidence topic report. Use of intravenous cyclizine in cardiac chest pain. (7/14)

A short cut review was carried out to establish whether cyclizine adversely affected haemodynamic parameters in patients with cardiac disease. A total of 70 papers were found of which one presented the best evidence to answer the clinical question. The author, date and country of publication, patient group studied, study type, relevant outcomes, results, and study weaknesses of this best paper are tabulated. The clinical bottom line is that cyclizine should be avoided in patients with acute coronary events.  (+info)

Acute eosinophilic pneumonia caused by calcium stearate, an additive agent for an oral antihistaminic medication. (8/14)

A 70-year-old man was admitted to our hospital because of dyspnea after taking an antihistaminic agent (homochlorcyclizine hydrochloride) for itching. Chest roentgenogram showed infiltration in the left lung field, and laboratory data revealed eosinophilia. Examination of the bronchoalveolar lavage fluid revealed an increased eosinophil count. A drug lymphocyte stimulation test was positive only for calcium stearate, an additive contained in the homochlorcyclizine hydrochloride tablet. The pulmonary infiltration and clinical symptoms subsided after withdrawal of all drugs and initiation of glucocorticoid therapy. Therefore, we concluded that this patient's pulmonary disease was caused by calcium stearate, an additive for an antihistaminic drug. An allergic reaction to a drug's additive material should be considered as a rare cause of drug-induced acute eosinophilic pneumonia.  (+info)

Cyclizine is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. Cyclizine is used in the prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness. Additionally, it has been used in the management of vertigo in diseases affecting the vestibular apparatus. Although the mechanism by which cyclizine exerts its antiemetic and antivertigo effects has not been fully elucidated, its central anticholinergic properties are partially responsible. The drug depresses labyrinth excitability and vestibular stimulation, and it may affect the medullary chemoreceptor trigger zone. It also possesses anticholinergic, antihistaminic, central nervous system depressant, and local anesthetic effects ...
Cyclizine is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. Cyclizine is used in the prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness. Additionally, it has been used in the management of vertigo in diseases affecting the vestibular apparatus. Although the mechanism by which cyclizine exerts its antiemetic and antivertigo effects has not been fully elucidated, its central anticholinergic properties are partially responsible. The drug depresses labyrinth excitability and vestibular stimulation, and it may affect the medullary chemoreceptor trigger zone. It also possesses anticholinergic, antihistaminic, central nervous system depressant, and local anesthetic effects ...
Cyclizine 2HCl is a piperazine derivative with Histamine H1 receptor antagonist activity. Buy Histamine Receptor inhibitor Cyclizine dihydrochloride from AbMole BioScience.
Calcium stearate is a carboxylate of calcium, classified as a calcium soap. It is a component of some lubricants, surfactants, as well as many foodstuffs. It is a white waxy powder. Calcium stearate is produced by heating stearic acid and calcium oxide: 2 C17H35COOH + CaO → (C17H35COO)2Ca + H2O It is also the main component of soap scum, a white solid that forms when soap is mixed with hard water. Unlike soaps containing sodium and potassium, calcium stearate is insoluble in water and does not lather well. Commercially it is sold as a 50% dispersion in water or as a spray dried powder. As a food additive it is known by the generic E number E470. Calcium stearate is a waxy material with low solubility in water, unlike traditional sodium and potassium soaps. It is also easy and cheap to produce, and exhibits low toxicity. These attributes are the basis of many of its applications. Related applications exist for the magnesium stearate. Calcium stearate is used as a flow agent and surface ...
Full text for this publication is not currently held within this repository. Alternative links are provided below where available. ...
Ive had it since 7 weeks now 13 weeks and its got worse even taking 3 cyclizine a day :( Not getting much hydration, managed to keep some toast down this morning but have chucked everything else back up and getting really worried I am not getting enough fluids. Theyve said I will get a call back within 2 hours. Has anyone else had any experiences calling 111 with sickness and what happened? People have been telling me to get checked out for days now but really felt I needed to today but what if Im just overreacting and wasting time? :(
Cortisone & Prednisolone: These are corticosteroids. If taken during the later part of pregnancy, these may cause deficiency of adrenal hormone on withdrawl of the drug. They delays growth and promote infection.. Cyclizine : The effects are the same as chlorocyclizine.. Cyclophosphamide: This has the same effects busulphan.. Dexamethasone: Its effects are the same as cortisone.. Dexamphetamine : This is used as a slimming drug. It may cause developmental defects of the heart in the foetus, if taken during pregnancy.. Diazepam: An anti-anxiety drug, if taken in a large quantity during late pregnancy, it may cause lowering of the body temperature and muscular weakness in the newborn baby.. Diazoxide: It may lead to abnormal distribution of foetal hair formation and hypoglycaemia in the new born baby.. Dicoumarol: Its effects are the same as bishydroxycoumarin.. Dihydrogesterone: It is likely to produce male characteristics in female babies.. Estrogens: If taken during pregnancy, they may cause ...
Herbs in tea will refresh and energise the physique and thoughts. Not restricted to the morning. ) and represent a life-threatening situation. Parejthood wrote an in depth post on several things that may planned parenthood colorado well be the culprit with easy solutions. A long cycle with out being pregnant is often as a consequence of not ovulating. I hit 13 weeks on Thursday. Ive been planned parenthood colorado my physician and he has prescribed me CYCLIZINE, Which is planned parenthood colorado assist with the sickness. Your physician will exhaust all commonplace testing options before offering a analysis of unexplained infertility. Unpasteurised milk. Kegel workouts strengthen your pelvic muscle groups and assist push back incontinence, both throughout pregnancy and after delivery. sixty three However, there is evidence that doing TENS is best than doing nothing in this type of pain. You plznned want to be sure that your doctor knows what happened along with your mother when she was ...
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Travelling m edical kit for Sports Medicine professionals International SportMed Journal, Vol.12 No. e.g. cyclizine hydrochloride. W.E. Medication use by.. Kaplan Meir survival analysis was used to determine. But the availability and the cost of the drug has been a prohibitive factor for the use of this drug in the.. dysfunction. I found out at 4 weeks and was on 1 mg/day of klonopin. Medications That Can Cause Chronic Fatigue - Drug Can zyvox be used for uti ...
Successful treatment of endometriosis by gynaecological laparoscopic surgery requires a different or alternative approach with low complication rates.
By now, the company has got a capacity of 15,000 metric tons for yellow lead oxide, (litharge, powder and granular), 10,000 metric tons for red lead oxide (powder and granular), 6,000 metric tons for lead silicate
By now, the company has got a capacity of 15,000 metric tons for yellow lead oxide, (litharge, powder and granular), 10,000 metric tons for red lead oxide (powder and granular), 6,000 metric tons for lead silicate
57) Abstract:. The invention relates to the pharmaceutical industry, in particular the production of medicines used for colds, relieving headaches and neuralgia. Analgesic antipyretic medication contains acetylsalicylic acid, paracetamol, caffeine, cocoa, starch, citric acid, sugar, talc, calcium stearate, and can additionally include polyvinylpyrrolidone (mol. mass 9900-35500, at a certain ratio of components. The method of obtaining new funds includes the preparation of raw materials, obtaining mass for tableting by mixing paracetamol, starch, caffeine, cocoa, moistening the mixture 45-50% solution of citric acid, 4,5-7,5% starch paste and 10-80% sugar syrup or 45-50% solution of citric acid and 10-80% sugar syrup, wet granulation, drying, dusting acetylsalicylic acid, starch, talc and calcium stearate, dry granulation. This is followed by tableting the resulting mass. The invention provides increased strength tablets. 4 C.p. f-crystals, 1 table.. The invention relates to pharmaceuticas is s, ...
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice ...
China Calcium Filler manufacturers - Select 2018 high quality Calcium Filler products in best price from certified Chinese Calcium Stearate manufacturers, Calcium Carbonate Masterbatch suppliers, wholesalers and factory on Made-in-China.com
7-[[(1R,4aR,6R,8aS)-5,5,8a-trimethyl-2-methylidene-6-oxidanyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]-6,8-dimethoxy-chromen-2-one,7-(2-chloroethyl)-1,3-dimethyl-8-(phenylmethyl)purine-2,6-dione,7-methoxy-3-(4-methoxy-2-oxidanyl-phenyl)-2,3-dihydrochromen-4-one,7-(fluoren-9-ylidenemethyl)bicyclo[4.4.1]undeca-1,3,5,7,9-pentaene-2-carbaldehyde,7,12-dimethyl-9-(trifluoromethyl)benzo[a]anthracene,7,12-dimethyl-10-(trifluoromethyl)benzo[a]anthracene,7-[(3,4-dimethoxyphenyl)methyl]-6-methyl-7H-thieno[2,3-c]pyridine,7-azanyl-2-methyl-6-methylsulfanyl-isoquinoline-3,5,8-trione,7-[[4-[[4-[(6,8-disulfonaphthalen-2-yl)diazenyl]-2-methoxy-5-methyl-phenyl]carbamoylamino]-5-methoxy-2-methyl-phenyl]diazenyl]naphthalene-1,3-disulfonic acid,7,8,9,10-tetrahydrobenzo[a]pyren-10-ol,7-ethyl-2-methyl-1,3,4,8,9,9a-hexahydropyrazino[1,2-c]pyrimidin-6-one,7-phenyl-5-[(4-sulfophenyl)amino]benzo[a]phenazin-7-ium-6-sulfonic acid,7-[[1-methyl-4-[[1-methyl-4-[[1-methyl-5-[[1-methyl-5-[(4,6,8-trisulfonaphthalen-2-yl
Not all of the side effects listed above have been reported for each of these medicines, but they have been reported for at least one of them. Buclizine, cyclizine, and meclizine are similar, so any of the above side effects may occur with any of these medicines.. Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.. Portions of this document last updated: March 01, 2017. Original article: http://www.mayoclinic.org/drugs-supplements/meclizine-buclizine-and-cyclizine-oral-route-parenteral-route/description/drg-20069630. Copyright © 2017 Truven Health Analytics Inc. All rights reserved. Information is for End Users use only and may not be sold, redistributed or otherwise used for commercial purposes.. ...
The dose of tramadol should not exceed the recommended maximum daily dose or the recommended dose for a single administration - see box below. To reduce the likelihood of serotonin syndrome occurring, avoid co-prescribing tramadol with the medicines listed in Table 1, if possible. Tramadol is contraindicated in patients who are taking monoamine oxidase inhibitors or who have taken them within the last 14 days.1 Prescribers also need to be aware that co-prescription of tramadol with tricyclic antidepressants, selective serotonin re-uptake inhibitors and antipsychotics can lower the seizure threshold.1 Prescribers should bear in mind the potential risks of serotonin syndrome and seizures when making a clinical decision to use tramadol.. Seizures have been reported with high doses of pethidine,3 morphine,4 cyclizine,5 and ondansetron.6 Metoclopramide may lower the seizure threshold in patients with epilepsy.7 Therefore, if it is necessary for tramadol to be administered with or immediately after ...
This medication is used to treat certain conditions of the stomach and intestines - price oral metoclopramide 5mg interaction cyclizine cheap get - perinorm 5mg metoclopramide castle o2 shop pulsatile pth treatment ulcers - want to buy metoclopramide discounts. Buy metoclopramide online
An absorbable biologically compatible putty-like composition is used as a matrix from which immunologically or pharmacologically active agents, such as antibiotics, can be introduced into the body to provide a slow sustained release of the agent over an extended period of time. A preferred matrix comprises a mixture of calcium stearate, dextran and castor oil.
Bichroma Light Blue / MBC-LB is a blue lustrous powder that is composed of Bismuth Oxychloride, Mica, Ferric Ammonium Ferrocyanide, and Calcium Stearate...
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Bed rest and administration of vestibular sedatives are required during acute attacks. Cinnarizine (15-30 mg t.i.d) or prochlorperazine 5-10 mg t.i.d) or prochlorperazine (5-10 mg t.i.d) suppress vertigo and vomiting. In more severe attacks, intramuscular injection of prochlorperazine 12.5 mg or cyclizine 50 mg may be required. Some authorities also give intravenous diuretics (frusemide 40 mg i.v.) to try to reduce the endolymphatic pressure. Prophylaxis from recurrent episodes is sometimes effective with vasodilators such as betahistine (8mg t.i.d.), but if disabling attacks continue or hearing deteriorates progressively, surgical endolymph drainage may be necessary ...
High affinity for PBP 2′ is crucial for the antibacterial activity of β-lactams against MRS. Unfortunately, none of the available β-lactam antibiotics sufficiently fulfils this requirement. This fact increasingly limits the therapeutic potential against staphylococcal infections of these otherwise very useful drugs.. However, the intensive search for new antistaphylococcal drugs has shown recently (1, 7, 11, 12, 14) that it is possible to achieve strong inhibition of PBP 2′ with selected β-lactam structures. Ro 63-9141 is a member of the class of pyrrolidinone-3-ylidenemethyl cephems, which show high potency against PBP 2′ of S. aureus but higher IC50s against normal, sensitive PBPs than other β-lactam antibiotics, e.g., methicillin and imipenem. This appears to be a common property of the pyrrolidinone-3-ylidenemethyl cephems, as it has been observed before for other members of this structural class (7). Ro 63-9141 shares features of cephalosporins with 7-aminothiazolylhydroxyimino ...
0005] Cyclic bis-phenol phosphates are another type of nucleating and clarifying agents suggested by Yutaka Nakahara et al. in U.S. Pat. No. 4,463,113 and Ryoji Kimura et al in U.S. Pat. No. 5,342,868 for polyolefins. Sodium 2, 2-methylene-bis-(4, 6-di-tert-butylphenyl) phosphate (NA-11) and Aluminium bis [2, 2-methylene-bis-(4, 6-di-tert-butylphenyl) phosphate (NA-21) are two popular products under this category. Many others commonly known compounds are kaolin, talc etc which show high polyolefin crystallization temperatures but exhibit many drawbacks for industrial applications. For example, Camphanic acid exhibits high peak crystallization temperature in PP homopolymer formulations but exhibits very poor thermal stability and plate out during processing. Sometimes sodium benzoate, NA-11, exhibit deleterious nucleating efficiency when used in combination with calcium stearate. This is due to calcium ion from the stearate transfers position with the sodium ions of the nucleating agents, ...
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(Fr: PnP éosinophilique aiguë). See also under Ic: Eosinophilic pneumonia. May cause ARF and ARDS. MV and/or ECMO may be needed. AEP is with diffuse pulmonary opacities, blood/BAL eosinophilia, pleural effusion and rapidly-progressive respiratory failure in the absence of a cause other than a drug or abused substance (e.g. parasitic infection). See also under IIb and XVb. Separating drug-induced vs. idiopathic AEP can be problematic (PMID 2761601)
The present invention relates to new crystalline molecular sieve SSZ-56 prepared using a trans-fused ring N,N-diethyl-2-methyldecahydroquinolinium cation as a structure-directing agent, methods for synthesizing SSZ-56 and processes employing SSZ-56 in a catalyst.
When a dosage form such as a tablet is made by compaction of a powdered composition, the composition is subjected to pressure from a punch and dye. Some excipients and active ingredients have a tendency to adhere to the surfaces of the punch and dye, which can cause the product to have pitting and other surface irregularities. A lubricant can be added to the composition to reduce adhesion and ease release of the product from the dye. Lubricants include magnesium stearate, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated castor oil;, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodiiun benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc and zinc stearate ...
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0212] Optionally one, two, three or more lubricants can be added to the formulations disclosed herein. Examples of pharmaceutically acceptable lubricants and pharmaceutically acceptable glidants include, but are not limited to, colloidal silica, magnesium trisilicate, starches, talc, tribasic calcium phosphate, magnesium stearate, aluminum stearate, calcium stearate, magnesium carbonate, magnesium oxide, polyethylene glycol, powdered cellulose and microcrystalline cellulose. The lubricant, e.g., may be present in an amount from about 0.1% to about 5% by weight of the composition; whereas, the glidant, e.g., may be present in an amount from about 0.1% to about 10% by weight. Lubricants are typically added to prevent the tableting materials from sticking to punches, minimize friction during tablet compression and allow for removal of the compressed tablet from the die. Such lubricants are commonly included in the final tablet mix in amounts usually less than 1% by weight. The lubricant component ...
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A method of operating a radar system, including the steps of digitally sampling a received signal at a predetermined sampling rate, to periodically provide a set of selected samples, the set of selected samples including positive going ramp samples, negative going ramp samples and CW burst samples and performing a first fast Fourier transform (FFT) on the positive going ramp samples, performing a second fast Fourier transform on the negative going ramp samples and performing a third fast Fourier transform on the CW burst samples is described. Utilizing the subsequent radar operations the method further includes the steps of tracking each resulting signal from the first fast Fourier transform performing steps, tracking each resulting signal from the second fast Fourier transform performing steps and tracking each resulting signal from the third fast Fourier transform performing steps and associating any resulting signals from the tracking steps to periodically provide output signals indicative of other
Get this from a library! Fast Fourier transform algorithms for parallel computers. [Daisuke Takahashi] -- Following an introduction to the basis of the fast Fourier transform (FFT), this book focuses on the implementation details on FFT for parallel computers. FFT is an efficient implementation of the ...
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A brief description of the FFAST algorithm. Fast fourier aliasing-based sparse transform Fast Fourier Aliasing-based Sparse Transform (FFAST) is a sparse FFT algorithm developed by
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Tremenza adalah obat yang digunakan untuk meringankan gejala-gejala flu karena alergi pada saluran pernapasan bagian atas yang memerlukan dekongestan nasal dan antihistamin. Isi tiap tablet adalah Pseudoephedrine HCl 60 mg dan Triprolidine HCl 2,5 mg. Selain berupa tablet, juga tersedia sediaan sirup. Tiap 5 ml (1 sendok takar) Tremenza Sirup mengandung Pseudoephedrine HCl 30 mg dan Triprolidine HCl…
The publication of the Cooley-Tukey fast Fourier transform (FFT) algorithm in 1965 has opened a new area in digital signal processing by reducing the order of complexity of some crucial computational tasks like Fourier transform and convultion from N 2 to N log 2 , where N is the problem size. The development of the major algorithms (Cooley-Tukey and split-radix FFT, prime factor algorithm and Winograd fast Fourier transform) is reviewed. Then, an attempt is made to indicate the state of the art on the subject, showin the standing of researh, open problems and implementations.... ...
The chemical I want to talk about today is a widely used and very useful chemical called N,N-diethyl-3-methylbenzamide. Most people know it by its acronym, DEET.. I was recently wondering just how DEET does its thing of making mosquitoes not bite people. (Why yes, the recent gap in my posts means I was on vacation. There may have been mosquitoes involved.) Obviously, I started by searching Google Scholar.. To my interest, it seems to be one of those (many) chemicals where science doesnt know exactly how it works, at least not well enough (yet) to synthesize a better fit based on that knowledge. There was some talk of specific chemical receptor targets in a few of the papers, but I didnt see anything in my searches about success in making a new repellent. From what I read, however, there is a pretty good understanding of the mechanism in general:. It seems mosquitoes think that humans smell tasty, and DEET smells bad.. Personally, I also think DEET spray smells bad, but it goes below my ...
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The possible role of the alpha-2 adrenoceptors in xylazine-induced vomiting and in motion sickness was investigated. Cats were divided into two groups according to motion sickness susceptibility and were observed after s.c. injections of xylazine. The incidence of vomiting increased with the dose, and at each dose, the high susceptibility group had a greater emetic incidence than the low susceptibility group. In another experiment with cats divided into two groups according to motion sickness susceptibility, s.c. administration of yohimbine effectively antagonized the xylazine-induced emesis in both susceptibility groups. The cats in the latter experiment were then challenged with a motion sickness stimulus, after s.c. pretreatment with yohimbine. Yohimbine failed to prevent motion sickness but did occasion an unexplained variability in the incidence of vomiting. These findings suggest that the emetic effect of xylazine results from stimulation of alpha-2 adrenoceptors but that these receptors ...
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A method and an apparatus for analyzing a portion of a sample, such as a minute pattern formed on a semiconductor substrate, by employing a Fast Fourier Transformation (FFT) method, in which a magnified image of a region of a sample to be analyzed is generated and converted into data having a frequency by the FFT method. The converted data are analyzed to determine whether the region of the sample is normal or abnormal. It is possible to measure and analyze the sample simultaneously and automatically by using the apparatus in accordance with the method for analyzing the sample.
Something called the fast Fourier transform is running on your cell phone right now. The FFT, as it is known, is a signal-processing algorithm that you use more than you realize. It is, according to the title of one research ...
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A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Idiopathic acute eosinophilic pneumonia
Abstract: Dengue hemorrhagic fever has been one of the major health problems in Indonesia. As the disease spreads out by Aedes aegypti, a variety of ways has been conducted to disconnect host, agent, and the environment chain including prevention of human contact with the vector using by various repellents. The present test compared the complete protection time of N,N-diethyl- 3-metatoluamide (DEET) and citronella oil impregnated in wet tissue against Aedes aegypti. For this test, an ethanol-based 12.5% DEET and 20% citronella oil were prepared, into which dry tissue papers were immersed, drain in open air, and then stored in aluminum foil packs for one day and one week. Meanwhile, a number of disease-free adult female Aedes aegypti were placed in mosquito cages. The prepared one-day and oneweek stored wet tissues were used to swab volunteer adult human hands (from elbow to wrist) which were then inserted into the mosquito cage in three replicates (25 mosquitoes each cage). Elapsed time from ...
The pharmacological actions of phenazocine, a new potent narcotic analgesic, have been shown to be qualitatively similar to those of morphine. Phenazocine, like morphine, produces analgesia, tolerance, respiratory depression, hypotension, bradycardia, colon spasm, excitation and mydriasis in cats, possesses antiemetic properties and its effects are antagonized by N-allylnormorphine. The results indicate, however, that phenazocine exhibits a greater separation than morphine between its analgesic activity on the one hand, and its cardiovascular-respiratory depressant effects in anesthetized dogs on the other. The separation of analgesic activity of phenazocine from undesirable effects was also demonstrated by phenazocines lack of emetic effect in dogs. The results of this study indicate that phenazocine is a promising agent for the treatment of pain.. ...
Fourier analysis is a rich and intensely complicated subject.. In general, the FT (Fourier Transform) is not the same as the FFT (Fast Fourier Transform). They give the same result for a finite time series with all the observations equally spaced in time ("evenly sampled"). But for an unevenly sampled time series, the FFT doesnt give the correct result - one is advised to use the DFT (Discrete Fourier Transform), and even that benefits from modification for best results. Thats one of the reasons there are so many variants (like the Lomb-Scargle modified periodogram or the Date-Compensated Discrete Fourier Transform), many of which have been reinvented multiple times under different names in different disciplines. With irregular time sampling a raw DFT can give misleading results, and these variants are especially popular (and useful!) in disciplines like astronomy for which the time sampling is rarely (if ever) even.. Also, it is possible to compute the FT for frequencies lower than the ...
Define eosinophilic pneumonia. eosinophilic pneumonia synonyms, eosinophilic pneumonia pronunciation, eosinophilic pneumonia translation, English dictionary definition of eosinophilic pneumonia. adj. 1. Easily stained by eosin or other acid dyes. Used of a cell or cell structure. 2. Of or relating to eosinophils. adj. having an affinity for eosin...
PubMed comprises more than 30 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.
Triprolidine is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose. Codeine is a narcotic cough suppressant. It affects the signals in the brain that trigger cough reflex. Phenylephrine is a decongestant...
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By Dr. Michael Wechsler Division of Pulmonary and Critical Care Brigham and Womens Hospital Harvard Medical School Boston, Massachusetts There are 2 main types
Designed for a first course in digital signal processing, Digital Signal Processing: Spectral Computation and Filter Design covers two major topics: the computation of frequency contents of signals and the design of digital filters. While it focuses on basic ideas and procedures and covers the standard topics in the field, this unique text distinguishes itself from competing texts by extensively employing the fast Fourier transform (FFT).

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... wholesaler and exporter of Cyclizine Hydrochloride at reasonable price. ... Product Name : Cyclizine Hydrochloride. Chemical Names : CYCLIZINE HCl; Dihydrochlorid; Marzine; Reis-fit; Marezine ... Cyclizine Hydrochloride is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. ... We have been striving to maintain high quality standards in the market by offering Cyclizine Hydrochloride. To comply with set ...
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What is Cyclizine - Meaning and definition - PallipediaWhat is Cyclizine - Meaning and definition - Pallipedia

Cyclizine is a sedative antihistamine with antimuscarinic activity.. Belongs to the class of piperazine derivatives used as ... Cyclizine (n.d.) In Pallipedia. Houston: IAHPC. Retrieved from https://pallipedia.org/cyclizine/. Accessed on ...
more infohttps://pallipedia.org/cyclizine/

Cyclizine
        -
        Antiemetics,  Piperazine Derivatives,  ATC:R06AE03,  ATC:R06AE04Cyclizine - Antiemetics, Piperazine Derivatives, ATC:R06AE03, ATC:R06AE04

Cyclizine Pharmacology Cyclizine is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. Cyclizine is ... Cyclizine Dosage Forms Liquid Cyclizine Indication For prevention and treatment of nausea, vomiting, and dizziness associated ... Although the mechanism by which cyclizine exerts its antiemetic and antivertigo effects has not been fully elucidated, its ...
more infohttp://pharmacycode.com/Cyclizine.html

Cyclizine Hydrochloride
        -
        Antiemetics,  Piperazine Derivatives,  ATC:R06AE03,  ATC:R06AE04Cyclizine Hydrochloride - Antiemetics, Piperazine Derivatives, ATC:R06AE03, ATC:R06AE04

Cyclizine Hydrochloride Dosage Forms Liquid Cyclizine Hydrochloride Indication For prevention and treatment of nausea, vomiting ... Cyclizine Hydrochloride Absorption No information avaliable Cyclizine Hydrochloride side effects and Toxicity No information ... Cyclizine Hydrochloride Patient Information No information avaliable Cyclizine Hydrochloride Organisms Affected Humans and ... Cyclizine is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. Cyclizine is used in the prevention ...
more infohttp://pharmacycode.com/Cyclizine_Hydrochloride.html

Cyclizine dihydrochloride | CAS 5897-18-7 | AbMole BioScience | Cyclizine dihydrochloride PriceCyclizine dihydrochloride | CAS 5897-18-7 | AbMole BioScience | Cyclizine dihydrochloride Price

Buy Histamine Receptor inhibitor Cyclizine dihydrochloride from AbMole BioScience. ... Cyclizine 2HCl is a piperazine derivative with Histamine H1 receptor antagonist activity. ... Cyclizine 2HCl is a piperazine derivative with Histamine H1 receptor antagonist activity. ...
more infohttp://www.abmole.com/products/cyclizine-dihydrochloride.html

Prolixin - Meclizine, Buclizine, And Cyclizine (Oral Route, Parenteral Route) - Drugs & SupplementsProlixin - Meclizine, Buclizine, And Cyclizine (Oral Route, Parenteral Route) - Drugs & Supplements

... cyclizine, and meclizine are used to prevent and treat nausea, vomiting, and dizziness associated with motion sickness, and ... Heart failure - Cyclizine may make the condition worse. Proper Use of Prolixin - Meclizine, Buclizine, And Cyclizine (Oral ... Buclizine, cyclizine, and meclizine may cause dryness of the mouth. For temporary relief use sugarless candy or gum, melt bits ... Buclizine, cyclizine, and meclizine are similar, so any of the above side effects may occur with any of these medicines. ...
more infohttps://pharmacypedia.org/drugs-and-supplements/prolixin-meclizine-buclizine-and-cyclizine-oral-route-parenteral-route/

Antiemetic - WikipediaAntiemetic - Wikipedia

Cyclizine. *Diphenhydramine (Benadryl). *Dimenhydrinate (Gravol, Dramamine). *Doxylamine. *Mirtazapine (Remeron) is an ...
more infohttps://en.wikipedia.org/wiki/Antiemetic

Cinnarizine - WikipediaCinnarizine - Wikipedia

Cyclizine. References[edit]. *^ a b c d e Terland O, Flatmark T (June 1999). "Drug-induced parkinsonism: cinnarizine and ...
more infohttps://en.wikipedia.org/wiki/Cinnarizine

Nausicalm Injection (50mg/ml cyclizine) 5 x 1ml Ampoules/Pack (Cyclizine 50mg/ml)Nausicalm Injection (50mg/ml cyclizine) 5 x 1ml Ampoules/Pack (Cyclizine 50mg/ml)

It contains cyclizine and you can buy Nausicalm Injection online from InhouseChemist.vu ... Cyclizine in Nausicalm injection 50mg is also thought to act directly on the vomiting centre of the brain by blocking the ... Cyclizine in Nausicalm Injection 50mg binds to the H1 histamine receptor found on smooth muscle cells and on the vascular ... Cyclizine in Nausicalm injection 50mg is thought to act by blocking the muscarinic receptors in brainstem areas regulating ...
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cholinergic antagonist (CHEBI:48873)cholinergic antagonist (CHEBI:48873)

cyclizine hydrochloride Mass :302.84200 Formula : C18H22N2.HCl C18H23ClN2 pancuronium bromide Mass :732.67000 Formula : ...
more infohttps://www.ebi.ac.uk/chebi/chebiOntology.do?chebiId=48873

Patent US5840334 - Self-binding shearform compositions - Google PatentsPatent US5840334 - Self-binding shearform compositions - Google Patents

... cyclizine hydrochloride; danthron; dexbromopheniramine maleate; dextromethorphan hydrobromide; diazepam; dibucaine; diclofenac ...
more infohttp://www.google.com/patents/US5840334?dq=6,205,432

The Management of Nausea at the End of LifeThe Management of Nausea at the End of Life

Cyclizine (meclizine). PO/SC: 25-50 mg q8 h (maxdose, 200 mg/d). ... less with cyclizine), constipation. Hydroxyzine (Atarax). PO/ ...
more infohttps://www.medscape.com/viewarticle/901769

Tranylcypromine (Oral Route) Before Using - Mayo ClinicTranylcypromine (Oral Route) Before Using - Mayo Clinic

Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.. Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.. ...
more infohttps://www.mayoclinic.org/es-es/drugs-supplements/tranylcypromine-oral-route/before-using/drg-20073226

Aplenzin Advanced Patient Information - Drugs.comAplenzin Advanced Patient Information - Drugs.com

Detailed drug Information for Aplenzin. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
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  • Some people using methadone recreationally combine cyclizine with their methadone dose, a combination that is known to produce strong psychoactive effects. (wikipedia.org)
  • Cyclizine is used to treat sickness, travel sickness , and problems affecting the inner ear and balance. (drowsydriving.org)
  • About Cyclizine for sickness. (drowsydriving.org)
  • you should go back to your GP maybe other medications might work for you if Cyclizine is too drowsy. (madeformums.com)