Little's Colchicine may be available in the countries listed below.
Ingredient matches for Little's Colchicine
Colchicine is reported as an ingredient of Little's Colchicine in the following countries:
- Singapore
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Little's Colchicine may be available in the countries listed below.
Colchicine is reported as an ingredient of Little's Colchicine in the following countries:
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Pamba may be available in the countries listed below.
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Demotick may be available in the countries listed below.
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In the US, Nesacaine (chloroprocaine systemic) is a member of the drug class local injectable anesthetics and is used to treat Local Anesthesia.
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In the US, Genasyme (simethicone systemic) is a member of the drug class miscellaneous GI agents and is used to treat Endoscopy or Radiology Premedication, Functional Gastric Disorder, Gas and Postoperative Gas Pains.
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In the US, Taxol (paclitaxel systemic) is a member of the drug class mitotic inhibitors and is used to treat Breast Cancer, Breast Cancer - Adjuvant, Breast Cancer - Metastatic, Kaposi's Sarcoma, Non-Small Cell Lung Cancer, Ovarian Cancer and Wilms' Tumor.
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Prosexol may be available in the countries listed below.
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The following drugs and medications are in some way related to, or used in the treatment of Intra- or Post-op SVT or Hypertension. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Atimos may be available in the countries listed below.
Formoterol is reported as an ingredient of Atimos in the following countries:
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Carboprost Tromethamine (USAN) is known as Carboprost in the US.
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Glossary
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Steocalcin may be available in the countries listed below.
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Intramin may be available in the countries listed below.
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Sulfat de Atropinã may be available in the countries listed below.
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Misostol may be available in the countries listed below.
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Cyplegin may be available in the countries listed below.
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Gastron may be available in the countries listed below.
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Paraclodin may be available in the countries listed below.
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Pyrantel Paste may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Pyrantel embonate (a derivative of Pyrantel) is reported as an ingredient of Pyrantel Paste in the following countries:
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Tiapaston may be available in the countries listed below.
Tiquizium Bromide is reported as an ingredient of Tiapaston in the following countries:
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Doprovet may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Doxycycline monohydrate (a derivative of Doxycycline) is reported as an ingredient of Doprovet in the following countries:
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Tozolden may be available in the countries listed below.
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Beta Ointment may be available in the countries listed below.
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Cystichol may be available in the countries listed below.
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Oxytocin Bengen may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Oxytocin is reported as an ingredient of Oxytocin Bengen in the following countries:
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Genta-Sulfat may be available in the countries listed below.
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Novo-Gesic may be available in the countries listed below.
Paracetamol is reported as an ingredient of Novo-Gesic in the following countries:
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Treating mild to moderate itching, redness, and swelling caused by certain skin conditions.
DesOwen Cream is a topical corticosteroid. It works by reducing skin inflammation (redness, swelling, itching, and irritation).
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with DesOwen Cream. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with DesOwen Cream. Because little, if any, of DesOwen Cream is absorbed into the blood, the risk of it interacting with another medicine is low.
Ask your health care provider if DesOwen Cream may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use DesOwen Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use DesOwen Cream.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Mild, temporary stinging or burning when first applied.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); acne-like rash; inflamed hair follicles; inflammation around the mouth; severe or persistent burning, irritation, redness, or swelling of the skin; thinning, softening, or discoloration of the skin.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: DesOwen side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision or other vision changes; muscle weakness; severe or persistent headache; symptoms of high blood sugar (eg, increased thirst or urination, confusion, unusual drowsiness); unusual weight gain, especially in the face.
Store DesOwen Cream at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store in a tightly closed container. Do not freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Keep DesOwen Cream out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about DesOwen Cream. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
The following drugs and medications are in some way related to, or used in the treatment of Non-Small Cell Lung Cancer. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Micromedex Care Notes:
Harvard Health Guide:
Class: Androgens
ATC Class: A14AA
VA Class: HS100
Chemical Name: 17β-Hydroxy-17-αmethyl-2-oxa-5α-androstan-3-one
Molecular Formula: C19H30O3
CAS Number: 53-39-4
Brands: Oxandrin
Peliosis hepatis, a condition in which the liver contains blood-filled cysts, reported with androgen therapy.1 4 30 31 34 May present with minimal hepatic dysfunction,1 4 34 or effects may not be apparent until complicated by life-threatening liver failure or rupture of the cysts resulting in intra-abdominal hemorrhage.1 4 5 7 31 34 (See Hepatic Effects under Cautions.)
Discontinuance of androgen therapy usually results in resolution of liver lesions.1 4 32 34
Liver cell tumors reported with androgen therapy.1 4 5 7 30 31 34 Tumors are usually benign and androgen dependent; hepatocellular carcinoma, sometimes fatal, also reported.1 4 5 7 34
Liver cell tumors associated with androgens are more vascular than other hepatic tumors; hepatic effects may not be apparent until complicated by life-threatening intra-abdominal hemorrhage.1 4 5 34
Discontinuance of androgen therapy often but not always results in regression or cessation of progression of the tumor.1 4 5 34
May markedly alter serum lipoprotein concentrations; decreased HDL- and increased LDL-cholesterol reported with androgen therapy.1 4 30 31 34 Consider increased risk of cardiovascular disease (e.g., atherosclerosis and CAD).1 4 31 34 (See Lipid Abnormalities under Cautions.)
Synthetic androgenic anabolic steroid hormone.1 4
Adjunct to conventional therapy to promote weight gain in individuals who experience weight loss following extensive surgery, chronic infections (e.g., HIV-associated wasting syndrome; designated an orphan drug by FDA for this use),3 or severe trauma (e.g., burns, spinal cord injury).1 5 17 19 22 32
Adjunct to conventional therapy for management of unexplained weight loss.1
Adjunct to conventional therapy to offset protein catabolism (e.g., muscle wasting, muscle pain or weakness, delayed wound healing, atrophy of protein matrix of bone) associated with long-term corticosteroid therapy.1 4 20 21 33
Labeled for the symptomatic treatment of bone pain accompanying osteoporosis.1 4 23
Androgens have been misused and abused by athletes, bodybuilders, weight lifters, and others to enhance athletic performance or physique†.6 7 8 9 10 32
Medical and sports experts (e.g., International Olympic Committee) consider such use to be inappropriate and unacceptable because of known adverse effects and potential long-term sequelae.9 Such misuse by athletes is contrary to rules and ethical principles of athletic competition.7 8 9 10
Manufacturer states that androgens have not been shown to enhance athletic performance.1
Individualize dosage and duration of therapy carefully according to individual requirements, response, and tolerance.1 4 Use the minimum effective dosage; intended for intermittent use.1 4 22
Administer orally 2–4 times daily in adults.1 4
≤0.1 mg/kg daily for 2–4 weeks.1 4 Repeat course of therapy intermittently as needed to maintain weight.1 4 32
Manufacturer states that a 2- to 4-week course of therapy usually is adequate to observe a response (i.e., slowing or cessation of weight loss).1 4 32 A longer period of treatment is necessary to regain lost weight, especially if ongoing catabolic stressors are present.32
Higher than recommended dosage of 0.1 mg/kg twice daily for 5 days to 12 months† has been evaluated in pediatric patients with burns.1 4 5 16 17 18 32
≤0.1 mg/kg daily.1 4 Manufacturer states that a 2- to 4-week course of therapy usually is adequate to observe a response.1 4 32 Repeat course of therapy intermittently as needed.1 4 32
2.5–20 mg daily in 2–4 divided doses for 2–4 weeks.1 4 Repeat course of therapy intermittently as needed to maintain weight.1 4 32
Manufacturer states that a 2- to 4-week course of therapy usually is adequate to observe a response (i.e., slowing or cessation of weight loss).1 4 32 A longer period of treatment is necessary to regain lost weight, especially if ongoing catabolic stressors are present.32 Continuous administration for 3–4 months has been evaluated in patients with HIV-associated wasting syndrome.5 19
2.5–20 mg daily in 2–4 divided doses.1 4 Manufacturer states that a 2- to 4-week course of therapy usually is adequate to observe a response.1 4 32 Repeat course of therapy intermittently as needed.1 4 32
2.5–20 mg daily in 2–4 divided doses.1 4 Manufacturer states that a 2- to 4-week course of therapy usually is adequate to observe a response.1 4 Repeat course of therapy intermittently as needed.1 4
5 mg twice daily for 2–4 weeks recommended.1 Repeat course of therapy intermittently as needed.1 (See Geriatric Use under Cautions.)
Males with breast cancer or known or suspected prostate cancer.1 4
Women with hypercalcemia associated with metastatic breast cancer.1 4 (See Hypercalcemia under Cautions.)
Known or suspected pregnancy.1 4 (See Fetal/Neonatal Morbidity and Mortality under Cautions.)
Nephrosis.1 4
Hypercalcemia.1 4 (See Hypercalcemia under Cautions.)
May cause fetal harm; potential for virilization of fetus.1 4
Fetotoxicity, embryotoxicity, infertility, and virilization of female offspring demonstrated in animals.1 4
Potentially serious and/or life-threatening adverse hepatic effects (e.g., peliosis hepatis, hepatic adenomas, hepatocellular carcinoma) associated with prolonged use of high dosages of androgens.5 6 7 9 10 22 (See Boxed Warning.)
If cholestatic hepatitis with jaundice occurs, or if liver function test results become abnormal during therapy, discontinue oxandrolone and investigate etiology of these disorders.1 4 Drug-induced jaundice usually is reversible after discontinuance of drug.1 4
Monitor liver function periodically.1 4 17 22
Possible hypercalcemia resulting from osteolysis in women with metastatic carcinoma of the breast.1 4 Monitor urine and serum calcium concentrations frequently during the course of androgen therapy in women with metastatic breast cancer.1 4 30
If hypercalcemia occurs, discontinue the drug.1 4 (See Contraindications under Cautions.)
Edema, with or without CHF, possible as a result of sodium and water retention and may be a serious complication in patients with preexisting cardiac, renal, or hepatic disease.1 4 30 (See Geriatric Use under Cautions.)
Potential for serious adverse effects (e.g., increased aggression,6 7 8 10 13 22 antisocial behavior,6 7 manic episode,6 22 depression,9 changes in libido,6 7 8 9 10 22 increased risk of cardiovascular disease,6 7 8 9 hepatotoxicity6 7 8 9 10 ) associated with misuse and abuse of androgens (see Misuse and Abuse under Uses); oxandrolone preparations currently subject to control under the Federal Controlled Substances Act of 1970, as amended by the Anabolic Steroids Control Act of 1990 and 2004, as schedule III (C-III) drugs.11 32
Virilization, including baldness, clitoral enlargement, deepening of voice, hirsutism, and menstrual irregularities, may occur in females.1 4 5 6 9 13
Monitor women receiving oxandrolone therapy for signs of virilization.1 4 If virilization occurs, promptly discontinue therapy.1 4 Some changes may not be reversible (e.g., clitoral enlargement, voice changes) after discontinuance of the drug; concomitant use of estrogen with androgens does not prevent these effects.1 4 6 7 32
Possible polycythemia, especially with high dosages of androgens.1 4 30 Perform periodic hemoglobin and hematocrit determinations in patients receiving high dosages of androgens.1 4 30
Anabolic steroids may suppress clotting factors II, V, VII, and X and prolong PT.1 4 (See Specific Drugs and Laboratory Tests under Interactions.)
Androgens may increase LDL-cholesterol and decrease HDL-cholesterol concentrations; consider the increased risk for cardiovascular disease.1 4 5 6 7 10 12 13 19 22 32 Lipid concentrations return to baseline values approximately 1 month after discontinuance of androgen therapy.22
Use with caution in patients with cardiovascular disease or risk factors for cardiovascular disease.1 4 Determine serum lipid concentrations periodically; adjust therapy accordingly.1 4
Category X.1 4 (See Fetal/Neonatal Morbidity and Mortality and also Contraindications under Cautions.)
Not known whether oxandrolone is distributed into milk.1 4 Discontinue nursing or the drug.1 4
May accelerate bone maturation without producing compensatory gain in linear growth, possibly resulting in compromised adult stature.1 4 10 The younger the child, the greater the risk of the drug compromising final mature stature.1 4
Use with extreme caution in children and only under the supervision of a specialist who is aware of the adverse effects of oxandrolone on bone maturation.1 4 Perform radiographic examination of the left hand and wrist every 6 months to determine rate of bone maturation and to assess the effect of treatment on epiphyseal centers.1 4
Possible increased risk of developing prostatic hypertrophy and prostate cancer during androgen therapy.1 4 30
Response in patients ≥65 years of age does not appear to differ from that in younger adults.1 Increased sensitivity to fluid retention and increases in hepatic transaminase values reported, particularly in geriatric women.1 Use lower dosage to minimize adverse effects.1 (See Geriatric Patients under Dosage and Administration.)
Elevated aminotransferases (ALT, AST),1 4 5 13 17 19 lipid abnormalities (e.g., decreased HDL cholesterol concentrations).1 4 5 13 19
Drug or Test | Interaction | Comments |
|---|---|---|
Anticoagulants, oral | May potentiate action of oral anticoagulants and decrease anticoagulant requirements1 4 22 24 26 32 Increases AUC and half-life of warfarin; minor bleeding reported;1 4 80-85% decrease in warfarin dosage (from a mean of 6.13 mg daily to a mean of 1.13 mg daily) were needed to maintain target INR of 1.5 in one study1 4 32 | Monitor PT or INR when oxandrolone therapy is initiated or discontinued in patients receiving oral anticoagulants and adjust anticoagulant dosage as needed1 4 32 Initial anticoagulant dosage may be substantially lower in patients receiving oxandrolone32 Monitor for signs and symptoms of occult bleeding1 4 |
Antidiabetic agents, oral (sulfonylureas) | Possible inhibition of sulfonylurea metabolism1 4 32 | Use concomitantly with care6 |
Corticotropin (ACTH) and corticosteroids | May exacerbate edema1 4 | Consider possibility of interaction before use13 |
Tests for thyroid function | Possible decreased thyroxine-binding globulin concentrations, resulting in decreased total serum thyroxine (T4) concentrations and increased resin uptake of triiodothyronine (T3) and T41 4 16 Free thyroid hormone concentrations remain unchanged1 4 May decrease protein-bound iodine (PBI) concentrations and radioactive iodine uptake1 4 |
Well absorbed after oral administration, with peak serum concentrations attained in approximately 1 hour.5 13
95%.5 13
Partially metabolized via sulfation to 17-epioxandrolone; other metabolites also identified.5 13 14 25 27 28
Excreted principally in urine as unchanged and unconjugated oxandrolone (28%).5 25 27
Biphasic; distribution half-life is 30 minutes and elimination half-life is approximately 10.4 hours in adults.1 5 25
In geriatric individuals, elimination half-life is 13.3 hours.1
20–25°C.4
Produces marked anabolic activity and relatively few androgenic effects.5 6 7 13 14 22
Produces retention of nitrogen,5 7 13 17 22 increases protein anabolism and amino acid utilization, and decreases urinary calcium concentrations.2 5 13 16 18 23
Increases lean body mass, body cell mass, and muscle strength.7 9 16 17 18 19 20 22
Increases bone mineral density and content.5 13 16 22
Inhibits protein catabolism induced by corticosteroids.5 6 8 17 22
Androgens stimulate production of erythrocytes, apparently by enhancing production of erythropoietin.22 (See Hematologic Effects under Cautions.)
Inhibits release of endogenous testosterone via feedback inhibition of pituitary luteinizing hormone (LH).1 4 7 8 10 19 22 32
Large doses of androgens may suppress spermatogenesis.1 4 6 7 8 9 22
Risk of virilization in females.1 2 4 6 Advise female patients to contact their clinician if they notice hoarseness, acne, menstrual changes, baldness, genital changes, or growth of facial hair.1 2 4
Risk of priapism; importance of males informing clinicians if too frequent or persistent penile erections occur.1 4
Advise male patients to contact their clinician if they notice new or worsening acne.1 4
Importance of periodic assessments to determine rate of bone maturation in pediatric patients.1 4
Importance of informing clinician if nausea, vomiting, changes in skin color, or ankle swelling occurs.1 4
Risk of potential liver toxicity and/or lipid abnormalities (e.g., increased LDL-cholesterol concentrations and decreased HDL-cholesterol concentrations.1 4 Importance of regular laboratory monitoring of liver function and cholesterol concentrations.1 4
Importance of women informing their clinician if they are or plan to become pregnant or plan to breast-feed.1 4
Importance of informing clinician of existing or contemplated concomitant therapy, including prescription (e.g., warfarin, antidiabetic medications) and OTC drugs and herbal supplements, as well as any concomitant illnesses.1 4
Importance of informing patients of other important precautionary information.1 4 (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Oxandrolone is subject to control under the Federal Controlled Substances Act of 1970, as amended by the Anabolic Steroids Control Act of 1990 and 2004, as a schedule III (C-III) drug.11
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
|---|---|---|---|---|
Oral | Tablets | 2.5 mg | Oxandrin ( C-III; scored) | Savient |
Oxandrolone Tablets ( C-III; scored) | ||||
10 mg | Oxandrin ( C-III) | Savient | ||
Oxandrolone Tablets ( C-III) |
This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.
Oxandrin 10MG Tablets (SAVIENT PHARMACEUTICALS INC.): 30/$822.73 or 60/$1621.34
Oxandrin 2.5MG Tablets (SAVIENT PHARMACEUTICALS INC.): 30/$249.24 or 90/$725.97
Oxandrolone 10MG Tablets (SANDOZ): 30/$535.96 or 90/$1577.85
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions April 2010. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
† Use is not currently included in the labeling approved by the US Food and Drug Administration.
1. Savient Pharmaceuticals. Oxandrin (oxandrolone) tablets prescribing information. East Brunswick, NJ; 2006 Jan.
2. AHFS consumer medication information. Oxandrolone. Bethesda, MD: American Society of Health-System Pharmacists; 2004 Oct 1. Available from website. Accessed 2008 Mar 7.
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