Mentored Hunting - Wisconsin Dnr, Metored

Wisconsin Department of Natural Resources

Your friends can "test drive" hunting through the DNR's Mentored hunting program. See more videos

Sign up for a Wingshooting clinic near you. Get involved mentor a new hunter today. Partner with the DNR and become a Wingshooting instructor. Take Aim! find a shooting range near you.

Contact information For information about the Learn to Hunt program, contact: DNR Customer Service Call Center Staff Available 7 Days a Week (7 a. m.-10 p. m.) Call Toll Free 1-888-WDNRINFo (1-888-936-7463)

Mentored hunting

It's easier than ever to introduce someone new to hunting in Wisconsin. Anyone 10 or older can now obtain a hunting license and hunt without first completing a hunter education course. He or she must be accompanied by a licensed hunter, hunt within arm's reach of the mentor, and follow other rules. Such mentored hunts remove barriers to hunting yet still allow people to safely experience hunting in a highly controlled manner. There are other ways people can Learn to Hunt in Wisconsin too.

This one-on-one mentoring opportunity gives first-time hunters a chance to try hunting and enables veteran hunters to pass on their passion for the outdoors and help keep Wisconsin's hunting heritage strong.

Rules for hunter

Must be at least 10 years old.

Must have the appropriate valid hunting license, permits and tags

May only hunt while within arm's reach of a "mentor" - regardless of the hunter's age or the mentor's age

Must follow all other hunting laws, seasons and bag limits

10 & 11 year olds may only hunt under these mentorship rules, even if they already completed hunter education

Only ONE firearm, bow or crossbow can be possessed jointly between the hunter and the mentor

Rules for mentor

Must be at least 18 year old

If born on or after 1-1-73, must be a hunter education course graduate, or have completed basic training with the U. S. Armed Forces

Must be the hunter's parent or guardian, or have the permission of the hunter's parent or guardian before acting as a mentor for a person under age 18

Must have a current year's hunting license. (Type of hunting license does not matter for the mentor, unless they will also be attempting to harvest game, in which case they must have the appropriate valid hunting license, permits and tags for species they are hunting.)

Only allowed to serve as a mentor for ONE hunter at a time if the hunter is either of the following:

age 10 or 11, or

was born on or after 1-1-73 and has not yet taken and passed a hunter education course.

Only ONE firearm, bow or crossbow can be possessed jointly between the hunter and the mentor

Additional information

Printable Mentored Hunting Pamphlet [PDF]

Programa de Caza con Mentor en Wisconsin [Spanish PDF]

Wisconsin txoj kev Saibxyuas Me nyuam plob hav zoov [Hmong PDF]

What Has Not Changed

Reduced License Fees for 10 or 11 Year Old Hunters

A person born on or after 1-1-73 who has not completed hunter education may only obtain a license that requires hunting with a mentor in compliance with the Hunting Mentorship Program rules.

A person who is at least 10 years old by the first day of the bear hunting season for which they are applying can now apply for a Class A bear hunting license or a bear hunting preference point.

A person who is age 9 or older may apply for a spring or fall turkey hunting permit, sharp-tailed grouse and Horicon goose permit. There is no minimum age to apply for a bobcat permit, but a person must be at least 10 before they obtain a license allowing hunting of bobcat.

Any person may apply to the DNR to transfer one or more of their hunting permits or licenses to a youth age 10-17 who is eligible to hunt. The transfer application must be made at least 15 days before that season begins.

It is legal for a youth of any age to possess a firearm (rifles, shotguns, or handguns) for the purpose of target practice, which also includes shooting trap, skeet or sporting clays, if accompanied by a parent or guardian, or a person age 18 or older designated by the parent or guardian. Note: the arms reach one firearm rule does not apply to target practicing.

Handguns may not be possessed or used for hunting by any one under age 18.

Contact information For information about the Learn to Hunt program, contact: DNR Customer Service Call Center Staff Available 7 Days a Week (7 a. m.-10 p. m.) Call Toll Free 1-888-WDNRINFo (1-888-936-7463)

Last revised: Tuesday May 03 2016

Medicort Disease Interactions, Medicort

Medicort (prednisolone) Disease Interactions

Corticosteroids (Includes Medicort) ↔ (+) Tuberculin Test

Severe Potential Hazard, High plausibility

Applies to: History - Tuberculosis, Tuberculosis -- Latent

In patients with latent tuberculosis or tuberculin reactivity, the use of pharmacologic dosages of corticosteroids may cause a reactivation of the disease. Close monitoring for signs and symptoms of tuberculosis is recommended if corticosteroid therapy is administered to patients with a history of tuberculosis or tuberculin reactivity. During prolonged corticosteroid therapy, tuberculosis chemoprophylaxis may be considered.

References

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

"Product Information. Deltasone (prednisone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Electrolyte Imbalance

Severe Potential Hazard, Moderate plausibility

Applies to: Hypernatremia, Hypokalemia, Seizures, Hypocalcemia

Corticosteroids can cause hypernatremia, hypokalemia, and fluid retention. These mineralocorticoid effects are most significant with fludrocortisone, followed by hydrocortisone and cortisone, then by prednisone and prednisolone. The remaining corticosteroids, betamethasone, dexamethasone, methylprednisolone, and triamcinolone, have little mineralocorticoid activities. However, large doses of any corticosteroid can demonstrate these effects, particularly if given for longer than brief periods. All corticosteroids also increase excretion of calcium and can cause hypocalcemia. Therapy with corticosteroids should be administered cautiously in patients with preexisting electrolyte disturbances. Caution is also advised when treating patients with seizure disorders, since electrolyte disturbances may trigger seizure activity.

References

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

Morris GC, Egan JG, Jones MK "Hypokalaemic paralysis induced by bolus prednisolone in Graves' disease." Aust N Z J Med 22 (1992): 312

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

View all 15 references

Corticosteroids (Includes Medicort) ↔ Gi Perforation

Severe Potential Hazard, Moderate plausibility

Applies to: Diverticulitis, Intestinal Anastomoses, Ulcerative Colitis

Corticosteroids may cause gastrointestinal perforation and hemorrhage, usually when given in high dosages or for prolonged periods. They may also mask symptoms of complications such as peritonitis or intraabdominal sepsis. Therapy with corticosteroids should be administered cautiously in patients with diverticulitis, nonspecific ulcerative colitis (if there is a probability of impending perforation, abscess, or other pyogenic infection), or recent intestinal anastomoses.

References

Fadul CE, Lemann W, Thaler HT, Posner JB "Perforation of the gastrointestinal tract in patients receiving steroids for neurologic disease." Neurology 38 (1988): 348-52

"Product Information. Deltasone (prednisone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

View all 18 references

Corticosteroids (Includes Medicort) ↔ Infections

Severe Potential Hazard, High plausibility

Applies to: Infection - Bacterial/Fungal/Protozoal/Viral

The immunosuppressant and anti-inflammatory effects of corticosteroids, particularly in higher dosages, may decrease host resistance to infectious agents, decrease the ability to localize infections, and mask the symptoms of infection. Secondary infections may be more likely to develop. In general, corticosteroids should not be used in patients with active infections, especially systemic fungal infections, unless they are medically necessary and effective antimicrobial therapy or other appropriate treatment has been instituted. However, for corticosteroid-dependent patients who develop a severe or life-threatening infection, continuation of corticosteroid therapy with at least physiologic replacement dosages should be considered, since these patients may have secondary adrenocortical insufficiency. Removal of external steroid during periods of stress may be detrimental to these patients.

References

"Product Information. Hydrocortone (hydrocortisone)." Merck & Co, Inc, West Point, PA.

Swartz SL, Dluhy RG "Corticosteroids: clinical pharmacology and therapeutic use." Drugs 16 (1978): 238-55

"Product Information. Hydeltrasol (prednisolone)." Merck & Co, Inc, West Point, PA.

View all 19 references

Corticosteroids (Includes Medicort) ↔ Mi

Severe Potential Hazard, Moderate plausibility

Applies to: Myocardial Infarction, Post MI Syndrome

The use of corticosteroids may be associated with left ventricular free-wall rupture in patients who have had a recent myocardial infarction. Pharmacologic dosages of corticosteroids should be administered with great caution in such patients.

References

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

"Product Information. Cortone Acetate (cortisone)." Merck & Co, Inc, West Point, PA.

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

View all 9 references

Corticosteroids (Includes Medicort) ↔ Ocular Herpes Simplex

Severe Potential Hazard, Moderate plausibility

Applies to: Ocular Herpes Simplex

Pharmacologic dosages of corticosteroids should be used cautiously in patients with ocular herpes simplex because of the risk of corneal perforation.

References

"Product Information. Deltasone (prednisone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

View all 9 references

Corticosteroids (Includes Medicort) ↔ Pud

Severe Potential Hazard, High plausibility

Applies to: History - Peptic Ulcer, Peptic Ulcer

Corticosteroids may cause peptic ulcer disease and gastrointestinal (GI) hemorrhage, usually when given in high dosages or for prolonged periods. However, even conventional dosages may aggravate symptoms in patients with a history of peptic ulcers. Delayed healing of ulcers has also been reported. Therapy with corticosteroids should be administered cautiously in patients with active or latent peptic ulcers or other risk factors for GI bleeding. Some clinicians recommend the use of prophylactic antacids or H2-antagonists between meals when large doses of corticosteroids are necessary.

References

Thomas TP "The complications of systemic corticosteroid therapy in the elderly." Gerontology 30 (1984): 60-5

Heimdal K, Hirschberg H, Slettebo H, Watne K, Nome O, Sletteb H "High incidence of serious side effects of high-dose dexamethasone treatment in patients with epidural spinal cord compression." J Neurooncol 12 (1992): 141-4

Weissman DE, Dufer D, Vogel V, Abeloff MD "Corticosteroid toxicity in neuro-oncology patients." J Neurooncol 5 (1987): 125-8

View all 21 references

Corticosteroids (Includes Medicort) ↔ Scleroderma

Severe Potential Hazard, Moderate plausibility

Applies to: Systemic Sclerosis

In patients with scleroderma, corticosteroids may precipitate renal crisis with malignant hypertension, possibly via steroid-induced increases in renin substrate and angiotensin II levels and decreases in vasodilator prostaglandin production. Renal failure may ensue. Therapy with corticosteroids should be administered cautiously in patients with scleroderma. In addition, they should be limited to short-term use.

References

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

"Product Information. Deltasone (prednisone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Strongyloidiasis

Severe Potential Hazard, High plausibility

Applies to: Strongyloidiasis

Unlike most helminths, Strongyloides stercoralis has the ability to replicate in the human host. In patients with strongyloidiasis, the use of pharmacologic or immunosuppressive dosages of corticosteroids may result in Strongyloides hyperinfection and dissemination with widespread larval migration, often accompanied by severe enterocolitis and potentially fatal gram-negative septicemia. Therapy with corticosteroids should be administered with extreme caution, if at all, in these patients.

References

"Product Information. Cortone Acetate (cortisone)." Merck & Co, Inc, West Point, PA.

"Product Information. Hydrocortone (hydrocortisone)." Merck & Co, Inc, West Point, PA.

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

View all 11 references

Corticosteroids (Includes Medicort) ↔ Depression/Psychoses

Moderate Potential Hazard, Moderate plausibility

Applies to: Depression, Psychosis

Corticosteroids may aggravate the symptoms of psychosis and emotional instability. Patients with these conditions should be monitored for increased or worsened symptoms during corticosteroid therapy.

References

"Product Information. Hydrocortone (hydrocortisone)." Merck & Co, Inc, West Point, PA.

Swartz SL, Dluhy RG "Corticosteroids: clinical pharmacology and therapeutic use." Drugs 16 (1978): 238-55

"Product Information. Cortone Acetate (cortisone)." Merck & Co, Inc, West Point, PA.

View all 27 references

Corticosteroids (Includes Medicort) ↔ Diabetes

Moderate Potential Hazard, High plausibility

Applies to: Diabetes Mellitus, Abnormal Glucose Tolerance

Corticosteroids can raise blood glucose level by antagonizing the action and suppressing the secretion of insulin, which results in inhibition of peripheral glucose uptake and increased gluconeogenesis. Therapy with corticosteroids should be administered cautiously in patients with diabetes mellitus, glucose intolerance, or a predisposition to hyperglycemia. Patients with diabetes mellitus should be monitored more closely during corticosteroid therapy, and their antidiabetic regimen adjusted accordingly.

References

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

Ludvik B, Clodi M, Kautzky-Willer A, Capek M, Hartter E, Pacini G, Prager R "Effect of dexamethasone on insulin sensitivity, islet amyloid polypeptide and insulin secretion in humans." Diabetologia 36 (1993): 84-7

Black DM, Filak AT "Hyperglycemia with non-insulin-dependent diabetes following intraarticular steroid injection." J Fam Pract 28 (1989): 462-3

View all 17 references

Corticosteroids (Includes Medicort) ↔ Fluid Retention

Moderate Potential Hazard, Moderate plausibility

Applies to: Fluid Retention, Congestive Heart Failure, Renal Dysfunction, Hypertension

Corticosteroids may cause hypernatremia, hypokalemia, fluid retention, and elevation in blood pressure. These mineralocorticoid effects are most significant with fludrocortisone, followed by hydrocortisone and cortisone, then by prednisone and prednisolone. The remaining corticosteroids, betamethasone, dexamethasone, methylprednisolone, and triamcinolone, have little mineralocorticoid activities. However, large doses of any corticosteroid can demonstrate these effects, particularly if given for longer than brief periods. Therapy with corticosteroids should be administered cautiously in patients with preexisting fluid retention, hypertension, congestive heart failure, and/or renal dysfunction. Dietary sodium restriction and potassium supplementation may be advisable.

References

Klepikov PV, Kutyrina IM, Tareyeva IE "Steroid-induced hypertension in patients with nephrotic syndrome." Nephron 48 (1988): 286-90

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

Pang S, Clark AT, Freeman LC, Dolan LM, Immken L, Mueller OT, Stiff D, Shulman DI "Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia." J Clin Endocrinol Metab 75 (1992): 249-53

View all 18 references

Corticosteroids (Includes Medicort) ↔ Hyperadrenocorticalism

Moderate Potential Hazard, High plausibility

Applies to: Hyperadrenocorticism, Hyperaldosteronism, Adrenal Tumor

Corticosteroids mimic the effects of endogenous cortisol and aldosterone. The use of these agents may aggravate conditions of hyperadrenocorticalism in a dose-dependent manner.

References

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

Lieberman P, Patterson R, Kunske R "Complications of long-term steroid therapy for asthma." J Allergy Clin Immunol 49 (1972): 329-36

"Product Information. Hydeltrasol (prednisolone)." Merck & Co, Inc, West Point, PA.

View all 14 references

Corticosteroids (Includes Medicort) ↔ Hyperlipidemia

Moderate Potential Hazard, Moderate plausibility

Applies to: Hyperlipidemia

Corticosteroids may elevate serum triglyceride and LDL cholesterol levels if used for longer than brief periods. Patients with preexisting hyperlipidemia may require closer monitoring during prolonged corticosteroid therapy, and adjustments made accordingly in their lipid-lowering regimen.

References

"Product Information. Florinef Acetate (fludrocortisone)." Bristol-Myers Squibb, Princeton, NJ.

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

"Product Information. Hydeltrasol (prednisolone)." Merck & Co, Inc, West Point, PA.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Hypothyroidism

Moderate Potential Hazard, Moderate plausibility

Applies to: Hypothyroidism

Corticosteroids may have enhanced effects in hypothyroidism due to decreased metabolism of these agents. Patients with hypothyroidism should be monitored more closely for excessive cortisol effects. Dosage adjustments may be required secondary to changes in their thyroid condition.

References

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Liver Disease

Moderate Potential Hazard, High plausibility

Applies to: Liver Disease

Corticosteroids are primarily metabolized by the liver and may have enhanced effects in patients with liver disease, especially cirrhosis. Dosage adjustments may be necessary in these patients.

References

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Deltasone (prednisone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Myasthenia Gravis

Moderate Potential Hazard, High plausibility

Applies to: Myasthenia Gravis

Although corticosteroids are commonly used in the treatment of myasthenia gravis to increase muscle strength, these agents should nevertheless be administered with caution in such setting. Patients should be treated in an intensive care unit and receive respiratory support, since muscle strength may markedly decrease initially, particularly with high dosages. Preferably, therapy should begin with relatively low dosages (15 to 25 mg/day of prednisone or equivalent) and increased stepwise as tolerated (approximately 5 mg/day of prednisone or equivalent at 2- to 3-day intervals until marked clinical improvement or a dosage of 50 mg/day is reached). Improvement may be delayed and gradual. Thus, it is important not to discontinue therapy prematurely.

References

Fauci AS, Braunwald E, Isselbacher KJ, Wilson JD, Martin JB, Kasper DL, Hauser SL, Longo DL, eds. "Harrison's Principles of Internal Medicine. 14th ed." New York, NY: McGraw-Hill Health Professionals Division (1998):

Corticosteroids (Includes Medicort) ↔ Myopathy

Moderate Potential Hazard, High plausibility

Applies to: Myopathy, Myoneural Disorder

Toxic myopathy has been observed with the chronic use or the administration of large doses of corticosteroids, often in patients with disorders of neuromuscular transmission such as myasthenia gravis or in patients receiving neuromuscular blocking agents. Fluorinated corticosteroids such as betamethasone, dexamethasone, and triamcinolone appear to cause more severe muscle atrophy and weakness than the nonfluorinated agents. Moreover, multiple-daily doses are more toxic than once-daily or, preferably, alternate-day morning doses. Steroid myopathy is generalized and sometimes accompanied by respiratory weakness and dyspnea. In some cases, it has resulted in quadraparesis. Elevations of creatine kinase may also occur, albeit infrequently. After withdrawal of corticosteroid therapy, recovery may be slow and incomplete. Therapy with corticosteroids should be administered cautiously in patients with preexisting myopathy or myoneural disorders, since these conditions may confound the diagnosis of steroid-induced myopathy. The presence of a normal serum CK level, minimal or no changes of myopathy on EMG, and type 2 muscle fiber atrophy on biopsy are helpful in suggesting steroid-induced weakness. If steroid myopathy is suspected, a dosage reduction or discontinuation of the steroid should be considered.

References

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

Seale JP, Compton MR "Side-effects of corticosteroid agents." Med J Aust 144 (1986): 139-42

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

View all 19 references

Corticosteroids (Includes Medicort) ↔ Ocular Toxicities

Moderate Potential Hazard, Moderate plausibility

Applies to: Glaucoma/Intraocular Hypertension, Cataracts

Prolonged use of corticosteroids may cause posterior subcapsular cataracts and elevated intraocular pressure, the latter of which may lead to glaucoma and/or damage to the optic nerves. Long-term therapy with corticosteroids should be administered cautiously in patients with a history of cataracts, glaucoma, or increased intraocular pressure.

References

Kobayashi Y, Akaishi K, Nishio T, Kobayashi Y, Kimura Y "Posterior subcapsular cataract in nephrotic children receiving steroid therapy." Am J Dis Child 128 (1974): 671-3

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

"Product Information. Cortone Acetate (cortisone)." Merck & Co, Inc, West Point, PA.

View all 19 references

Corticosteroids (Includes Medicort) ↔ Osteoporosis

Moderate Potential Hazard, High plausibility

Applies to: Osteoporosis

Corticosteroids reduce osteoblastic function and inhibit the absorption of intestinal calcium, which can result in bone resorption and bone loss during prolonged therapy. In addition, bone matrix may be affected by the protein-catabolic effects of corticosteroids, especially when given in high dosages or for prolonged periods, leading to aseptic necrosis and fractures. Long-term or high-dose corticosteroid therapy should be administered cautiously and only if necessary in patients with or at risk for osteoporosis. Adverse skeletal effects may be minimized by alternate-day or intermittent administration. Any patient receiving prolonged therapy with the equivalent of 7.5 mg prednisone/day or more are at risk for glucocorticoid-induced osteoporosis and should be managed according to The American College of Rheumatology (ACR) guidelines.

References

Anderton JM, Helm R "Multiple joint osteonecrosis following short-term steroid therapy. Case report." J Bone Joint Surg Am 64 (1982): 139-41

"Product Information. Decadron (dexamethasone)." Merck & Co, Inc, West Point, PA.

Goldstein MF, Fallon JJ, Harning R "Chronic glucocorticoid therapy-induced osteoporosis in patients with obstructive lung disease." Chest 116 (1999): 1733-49

View all 36 references

Corticosteroids (Includes Medicort) ↔ Prematurity

Moderate Potential Hazard, Moderate plausibility

Applies to: Prematurity/Underweight in Infancy

The use of certain parenteral formulations of dexamethasone, hydrocortisone, methylprednisolone, prednisolone and triamcinolone is considered by the drug manufacturers to be contraindicated in neonates, particularly premature infants and infants of low birth weight. Some formulations of these drugs contain benzyl alcohol which, when used in bacteriostatic saline intravascular flush and endotracheal tube lavage solutions, has been associated with fatalities and severe respiratory and metabolic complications in low-birth-weight premature infants. However, many experts feel that, in the absence of benzyl alcohol-free equivalents, the amount of the preservative present in these formulations should not necessarily preclude their use if they are clearly indicated. The American Academy of Pediatrics considers benzyl alcohol in low doses (such as when used as a preservative in some medications) to be safe for newborns. Continuous infusions of high dosages of medications containing benzyl alcohol may, however, cause toxicity and should be avoided if possible.

References

"Product Information. Medrol (methylprednisolone)." Pharmacia and Upjohn, Kalamazoo, MI.

"Product Information. Celestone (betamethasone)." Schering Corporation, Kenilworth, NJ.

""Inactive" ingredients in pharmaceutical products: update (subject review). American Academy of Pediatrics Committee on Drugs. Available from: URL: http://www. aap. org/policy/re9706.html." Pediatrics 99 (1997): 268-78

View all 10 references

Corticosteroids (Includes Medicort) ↔ Thromboembolism

Moderate Potential Hazard, Low plausibility

Applies to: Thrombotic/Thromboembolic Disorder, History - Thrombotic/Thromboembolic Disorder

Corticosteroids may increase blood coagulability and have rarely been associated with the development of intravascular thrombosis, thromboembolism, and thrombophlebitis. Therapy with corticosteroids should be administered cautiously in patients with thrombotic or thromboembolic disorders.

References

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

"Product Information. Hydeltrasol (prednisolone)." Merck & Co, Inc, West Point, PA.

"Product Information. Florinef Acetate (fludrocortisone)." Bristol-Myers Squibb, Princeton, NJ.

View all 10 references

Corticosteroids (Includes Medicort) ↔ Vaccination

Moderate Potential Hazard, High plausibility

Applies to: Vaccination

The administration of live or live, attenuated vaccines is contraindicated in patients receiving large or immunosuppressive doses of corticosteroids. Inactivated viral or bacterial vaccines should be used with caution, since their administration may pose a risk of neurological complications in these patients. Additionally, a diminished or inadequate serum antibody response may be anticipated. Immunization may be undertaken in patients receiving corticosteroids as replacement therapy, such as for Addison's disease.

References

"Product Information. Florinef Acetate (fludrocortisone)." Bristol-Myers Squibb, Princeton, NJ.

"Product Information. Kenalog (triamcinolone)." Bristol-Myers Squibb, Princeton, NJ.

"Product Information. Hydeltrasol (prednisolone)." Merck & Co, Inc, West Point, PA.

View all 10 references

Medicort (prednisolone) drug Interactions

There are 721 drug interactions with Medicort (prednisolone)

Medicort (prednisolone) alcohol/food Interactions

There are 2 alcohol/food interactions with Medicort (prednisolone)

See also.

Drug Interaction Classification

The classifications below are a general guideline only. It is difficult to determine the relevance of a particular drug interaction to any individual given the large number of variables.

Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.

Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.

Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.

Do not stop taking any medications without consulting your healthcare provider.

Disclaimer: Every effort has been made to ensure that the information provided by Multum is accurate, up-to-date and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. Multum's information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill, knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective, or appropriate for any given patient. Multum Information Services, Inc. does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. Copyright 2000-2016 Multum Information Services, Inc. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse, or pharmacist.

How to Prevent Deadly Drug Interactions

Exondys 51 Eteplirsen is a morpholino antisense oligomer for the treatment of Duchenne muscular dystrophy.

Yosprala Yosprala (aspirin and omeprazole) is a platelet aggregation inhibitor and proton pump inhibitor.

Cuvitru Cuvitru (immune globulin subcutaneous (human)) is indicated as replacement therapy in the treatment.

Erelzi Erelzi (etanercept-szzs) is a tumor necrosis factor (TNF) blocker biosimilar to Enbrel indicated.

FDA Consumer Updates

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Supreme Mpa Lite – Apps Para Android No Google Play, Mpa-Beta

Descricao

Supreme MPA - The Official Hip Hop App

Music Production App, MPC, Drum machine, Drum pads, Piano keyboard, sample editor, music sequencer for Recording mixing playing and sharing your own mobile music creations.

KITKAT 4.4 UPDATE COMING SOON! Android™ 4.0 Ice Cream Sandwich officially supported.

Designed by Supreme the Beatmaker, the legendary hip-hop producer and beatmaking teacher from Sunz of Man / Wu-Tang Clan fame.

Create your own hip-hop beats using 16 realtime pads (12 for Android 2.x and 3.x), piano keyboard and the visual Grid editor. Use the builtin samples, your own WAV/AIFF samples or cut an MP3 from your Music folder. Put together a complete song via the Song Editor. Export your project as MP3 and share it with your friends.

The only music production app designed by hip-hop producers for hip-hop producers.

The Lite version has the following limitations: - Song Editor is not available, and you can't export your song - Max 12 samples per project - Max 16 sequences - Everything else is available - managing multiple projects, adding unlimited samples to the library, keyboard, grid and all other features are open

Some rare devices have bugs that prevent Supreme MPA from working properly. Please try MPA Lite before buying MPA Full.

Contact us at supreme@supremempa. com for questions or support.

We are willing to work with you if you experience problems on your specific device. We can't reply to your reviews, so if you do have a problem, please contact us by email (supreme@supremempa. com) if you would like to have your problem fixed. We always respond!

Thanks for using Supreme MPA!

Supremo MPA - O Hip Hop Oficial App

Producao Musical App, MPC, drum machine, blocos de percussao, teclado de piano, editor da amostra, sequenciador de musica para gravacao de mistura de jogo e compartilhar suas proprias criacoes de musica movel.

KitKat 4.4 ATUALIZACAO EM BREVE! Android ™ 4.0 Ice Cream Sandwich oficialmente suportado.

Projetado pelo Supremo o Beatmaker, o produtor de hip-hop e lendario professor beatmaking de Sunz da fama Man / Wu-Tang Clan.

Crie suas proprias batidas de hip-hop com 16 almofadas em tempo real (12 para Android 2.x 3.x), teclado de piano eo editor grade visual. Use as amostras embutidas, as suas proprias amostras de WAV / AIFF ou cortar um MP3 da pasta Music. Coloque junto uma musica completa via Song Editor. Exportar seu projeto como MP3 e compartilha-lo com seus amigos.

O unico app de producao musical concebido pelos produtores de hip-hop para os produtores de hip-hop.

A versao Lite tem as seguintes limitacoes: - Song Editor nao esta disponivel, e voce nao pode exportar sua musica - Max 12 amostras por projeto - Max 16 sequencias - Tudo o resto esta disponivel - gerenciamento de multiplos projetos, acrescentando amostras ilimitadas para a biblioteca, teclado, rede e todos os outros recursos estao abertas

Alguns dispositivos raros tem bugs que impedem Supremo MPA de funcionar adequadamente. Por favor, tente MPA Lite antes de comprar MPA completa.

Contacte-nos em supreme@supremempa. com para duvidas ou suporte.

Estamos dispostos a trabalhar com voce, se voce tiver problemas em seu dispositivo especifico. Nao podemos responder a seus comentarios, por isso, se voce tem um problema, por favor contacte-nos por e-mail (supreme@supremempa. com) se voce gostaria de ter seu problema resolvido. Nos sempre responder!

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Natural - The Skeptic S Dictionary, Enatral

From Abracadabra to Zombies | View All

natural

FDA has not developed a definition for use of the term natural or its derivatives. However, the agency has not objected to the use of the term if the food does not contain added color, artificial flavors, or synthetic substances. --FDA

Something present in or produced by nature is natural , such as an earthquake or typhoon, or a poisonous mushroom. Death is natural in the sense that to die is to conform to the ordinary course of living things in nature . For a diabetic to die from lack of insulin would be natural. It would be unnatural for a diabetic to inject natural or synthetic insulin, since injections are not natural. Rotting wood on your porch is natural in the sense that you have not used anything artificial to protect it. The smell of rotting garbage is natural. Meanness and cruelty are natural to some people; that is, they are inherent, non-acquired personal traits . Some people are apparently natural born killers. Squishing bugs and kicking cats is natural for some people, in the sense that they do such things spontaneously, without reflecting on their actions. Nudity is the only natural state for animals, even humans. All clothing is artificial . that is, not natural . So are the fillings in your teeth. So is all make-up and jewelry. Bearded men are natural. To shave is to do something unnatural. The present Pope commits an unnatural act every day!

Just because something is natural does not mean that it is good, safe or healthy. Herbs are natural but they are also drugs when used in the diagnosis, treatment, or prevention of a disease. The chemicals which comprise synthetic drugs are natural. St. John's Wort (Hypericum perforatum) is natural, but it is a drug. Why do some people say that they prefer St. John's Wort to drugs for depression? If someone said that he preferred Irish whiskey to alcohol, we'd think he was confused. St. John's Wort contains hypericin, which inhibits monoamine oxidase, a chemical associated with depression. In other words, St. John's Wort (hypericin) is an "MAO inhibitor". MAO inhibitors are commonly prescribed by medical doctors to treat depression. Other types of anti-depressants have become more popular because they have far fewer side effects. MAO inhibitors should not be used when a person eats substances containing the amino acid tyramine or bacteria with enzymes that can convert tyrosine to tyramine, viz. alcoholic beverages, products made with yeast, aged cheese, sour cream, liver, canned meats, salami, sausage, pickled herring, eggplant and soy sauce. Otherwise, convulsions, extremely high fever and death by natural causes may occur.

Some plants are lethal even though they are natural. But if you die from eating a lethal but natural plant, you will not be said to have died of natural causes. Ditto, if you die from being bitten by a poisonous snake whose venom is quite natural. If you die from lung cancer caused by smoking tobacco, a natural plant, you will, however, be said to have died of natural causes.

[ new ] Foxgloves are natural and so are their cardiac glycosides. Purified, these chemicals can be used to treat cardiac problems (digitalis). The plant itself is highly toxic, however. Pick a few and eat them; you'll be dead before you know what hit you. If you want cardiac glycosides for your heart, you'll be better off with the synthesized version from a pharmaceutical firm. Those of you who use marijuana to prevent or cure your cancer the natural way might like to know that the current scientific research indicates that synthesized cannabinoids are likely to be more useful as cancer drugs than natural pot or homemade oil because they can isolate helpful chemicals from harmful ones and control dosage and purity much more effectively than pot growers do.* [/ new ]

Fleas on dogs are natural. Flea collars are unnatural. Mosquitoes and flies are natural, though most people find them to be a nuisance and prefer the unnatural comfort of mosquitoeless nights and flyless barbecues. Eating meat might be a natural act, but eating cooked meat is unnatural. Most sauces put on meat are made with both natural and artificial ingredients. Salt is natural, but some healthy people avoid salt like the plague.

Civilization is unnatural. Indoor plumbing is unnatural. Corrective lenses are unnatural. So are automobiles. Think about that the next time you drive to the garden shop to get some natural fertilizer for your garden or to your naturalist herb shop for a little pick-me-up.

To have a broken arm set by a physician is unnatural. To let it heal spontaneously would be natural, even if debilitating for life. Getting a medical degree is unnatural. Foraging and experimenting by trial and error would be natural, even if often lethal. Children born with no brains or other monstrous deformities are natural. Brain surgery to remove a tumor is unnatural.

Anything supernatural is unnatural but is usually considered to be good by those who believe in the supernatural. Reading and writing are unnatural. Urinating whenever one has the urge is natural, but uncivilized. Marijuana is natural, so it must be good, right? LSD is unnatural, though mescaline is natural. Ergot is natural. Mold and bacteria and viruses are natural. Arsenic is natural. To strike back when struck is natural, but considered unchristian. Turning the other cheek when struck is considered Christian but it is unnatural.

Monogamy is natural among some mammals, but unnatural for most mammals. Reproduction is natural but marriage is unnatural. Using condoms is unnatural. Dying of AIDS is to die of natural causes. Herpes is natural. Raping women is natural to some men, but it is usually regarded as evil nonetheless. Pedophilia seems to be natural in some people, but does that make it good?

In fact, ultimately everything which is made is comprised of nothing but natural atoms, molecules, elements, or substances. So, if everything is basically natural, why do some people, such as the naturopaths. make such a big fuss about using only what is natural? Such an obsession seems unhealthy, but it helps one avoid having to ask difficult questions about whether something really is good, safe or healthy. All you need to know is that something is "natural" and you don't have to think about its value.

Note . The naturalistic fallacy is what some skeptics have called the belief that medicines that are natural are somehow magically safe and effective or, more generally, the belief that if something's natural, it's good . In logic, however, a false or questionable belief is not, in itself, considered a fallacy. A fallacy is an error in reasoning, not an error in belief. This herb is natural, therefore it is safe and effective would be a fallacy. All herbs are safe and effective would be a false belief. It is very unlikely that even the most ardent advocate of natural cures is so ignorant as to believe that anything that is natural is good for you. Defenders of natural cures may believe that when there are natural remedies and artificial remedies, like synthetic drugs, for the same health issue that the natural remedy is preferable to the drug. They would be wrong, as indicated by the examples above regarding digitalis and drugs with synthetic cannabinoids. Frequently, one finds the naturalists claiming that this is so because there are likely to be fewer side effects from the natural remedy or that there is likely to be some unknown natural accompaniment to, say, vitamin C in fruit and synthesized vitamin C tabs. Sometimes, however, the side effects of the natural plant can be harmful and synthetic drugs that isolate and purify the active salutary chemicals in a plant are a much wiser choice.

To believe that herbs are always better for you than drugs is a false belief. To believe that organic food is always better for you than food that has been grown using synthetic herbicides, pesticides, or fertilizers is to hold a false belief. To argue that one should always take herbs or some natural food rather than drugs for pneumonia because natural products are always better for you than antibiotics is to argue fallaciously. To argue that one should always eat organic foods because they are healthier foods than conventionally grown foods is to argue fallaciously.

The term 'naturalistic fallacy' has a history in the discipline of moral philosophy. The English philosopher G. E. Moore (1873-1958) argued that since moral values such as 'goodness' are indefinable, it is wrong to identify such things as pleasure or utility as identical to goodness. He called reasoning that just because, as some might argue, the pleasurable is good does not mean that good is defined by pleasure. He called such reasoning the naturalistic fallacy. He believed that moral values are not natural properties of anything that might be studied scientifically because values are prescriptive, not descriptive. Moral values refer to what we ought to do, not to what we do. Whether Moore's views on moral values are correct or acceptable is debatable. In any case, there seems little to be gained by calling false beliefs about natural cures examples of the naturalistic fallacy. As I said, it is highly unlikely that even the dimmest nature cure advocate believes that having the property of being natural is identical to having the property of being beneficial to your health or that there is some kind of moral imperative to seek anything that is natural.

Sometimes one sees the expression 'appeal to nature ' to refer to the fallacious argument that "a thing is good because it is 'natural', or bad because it is 'unnatural'." Such a designation is pointless since these arguments obviously beg the question. We might say they have the grammatical form of arguments but they are really statements, both of which are obviously false: Anything natural is good; anything unnatural is bad. The so-called 'appeal to nature' is not really an argument and, I repeat, not a position you are likely to find held by even the most demented believer in natural cures. But I could be wrong. There may be somebody out there who won't brush or floss his teeth because it's unnatural and therefore bad for your health.

Natural Does Not Mean Safe Herbal supplements are unregulated, overhyped, and potentially deadly. By Geoffrey Kabat "Between 1994 and 2008, the number of dietary supplement products on the market increased from 4,000 to 75,000. In the first 10 months of 2008, the FDA received nearly 600 reports of serious adverse events (including hospitalization, disability, and death) from these products and 350 reports of moderate or mild adverse events. However, the FDA believes that these reports are drastically underreported and estimates that the annual number of all adverse events is 50,000."

Health Canada pulls unauthorized arthritis pills (Specific-Formula Arthro-Ace, sold as a "natural" health product, was found to contain dexamethasone, a steroidal prescription drug used to treat inflammatory conditions such as arthritis and allergic reactions.)

Komezol, Komezol

Omeprazole

Click for further information on drug naming conventions and International Nonproprietary Names .

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Product Description Common use This medicine is a proton pump inhibitor (PPI) used to treat ulcers, heartburn, gastroesophageal reflux, erosive esophagitis, or Zollinger-Ellison syndrome and also ulcers generated by long-term use of non-steroidal anti-inflammatory drugs (NSAIDs). To treat ulcers caused by bacterial infections this medicine may be used in combination with antibiotics such as amoxicillin or clarithromycin. Prilosek significantly alleviates such their symptoms as heartburn, difficulty swallowing, coughing, and sleep problems. Prilosek works by blocking acid production in the stomach. The medicine may be used to treat other conditions diagnosed by your doctor.

Dosage and directions Follow all the directions provided by your doctor. Take this medication (15-30 mg) orally once a day in morning before a meal with a full glass of water or according to your doctor's recommendations. Swallow the tab whole, do not chew, crush, or open the capsule as may destroy the drug and/or increase side effects. Antacids drugs can be taken together with this medicine, if necessary. Dosage and duration of treatment depends on your medical condition and response to the therapy. Take it the same time each day to avoid missing a dose. In the case of aggravation or worsening of your illness notify your doctor immediately. It may take 1 - 4 days before Prilosek acts in full measure. Treatment with Prilosec should not be stopped even if certain amelioration is achieved. Improvement of symptoms is observed within 4 to 8 weeks in treatment of gastric ulcers or reflux disease. Treatment of heartburn usually lasts for 14 days. If heartburn persists after this period of time or even worsens, or if you need more than one course of treatment every 4 months, contact your doctor or pharmacist.

Precautions Prilosec is not recommended during pregnancy. Breastfeeding when using this drug is not recommended as it is not known whether it gets into breast milk. Tell your doctor if allergic reaction appears. Your doctor or pharmacist should be aware of your health problems, to provide health care, especially if you have problems such as liver disease, other stomach problems (e. g. tumors), heartburn over 3 months, unexplained weight loss, constant nausea/vomiting /stomach pain, blood in vomit or black stools. Some symptoms may witness about a more serious condition. This medicine may cause dizziness. Be careful performing work associated with concentration of attention, such as driving or operating mechanisms. Restrict consumption of alcoholic beverages. Start or interruption in taking any medicine should be be approved by your doctor. If you do not notice any improvement of your symptoms or if they even become worse, inform your doctor about it. Do not share this medicine with anybody with similar symptoms. Do not use this medicine to treat other diseases.

Possible side effects Adverse reactions that may disappear during treatment include headache, constipation, cough, dizziness, or rash. If they continue or are bothersome, let your doctor know about it. An allergic reaction to this medicine is not expected, but seek immediate medical help if it happens. Symptoms of an allergic reaction appear as rash, itching, dizziness, swelling, or difficult breathing. If you notice other reactions of your body which are not listed above, contact your doctor or pharmacist.

Prilosec can decreases elimination of diazepam, warfarin and phenytoin. These are medications metabolized in the liver by oxidation. Drugs which are metabolized with help of cytochrome P-450 system (e. g. cyclosporine, disulfiram, benzodiazepines) may also interact with Prilosec because it is metabolized the same way. Clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with Prilosec may result in increases in plasma levels of Prilosec. Concomitant use of Prilosec and clarithromycin may result in increases in plasma levels of erithromycin, and 14-hydroxy-clarithromycin. You may need additional monitoring of your condition if you are taking ampicillin, cilostazol, cyclosporine, diazepam, digoxin, disulfiram, iron, itraconazole, ketoconazole, moclobemide, phenytoin, sucralfate, vorconizole, or warfarin. This medicine may be combined with antacids if they were prescribed by your doctor. Potent acid-reducing drugs such as Prilosec diminish the effectiveness of sucralfate, and other medicaitons such as the antifungals ketoconazole and itraconazole. If instructed to take any of these medicines while taking Prilosec, consult your doctor or pharmacist regarding the proper timing of each dose, usually Prilosec is taken 30 minutes before sucralfate.

Missed dose If you missed a dose take the medication as soon as you remember. If it is almost time of your next dose, just skip its intake and return to your regular schedule.

Overdose If suppose that took too much of Prilosec contact your local poison control center or emergency room immediately. Symptoms of overdose are confusion, blurred vision, unusual sweating, or unusually fast heartbeat.

Storage Store at room temperature between 59-77 F (15-25 C). Do not expose to high humidity or keep in a bathroom. Hide Prilosec away from children and pets. If your treatment requires an extended period of time, take care about refills before your supply is over.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use This medicine is a proton pump inhibitor (PPI) used to treat ulcers, heartburn, gastroesophageal reflux, erosive esophagitis, or Zollinger-Ellison syndrome and also ulcers generated by long-term use of non-steroidal anti-inflammatory drugs (NSAIDs). To treat ulcers caused by bacterial infections this medicine may be used in combination with antibiotics such as amoxicillin or clarithromycin. Prilosek significantly alleviates such their symptoms as heartburn, difficulty swallowing, coughing, and sleep problems. Prilosek works by blocking acid production in the stomach. The medicine may be used to treat other conditions diagnosed by your doctor.

Dosage and directions Follow all the directions provided by your doctor. Take this medication (15-30 mg) orally once a day in morning before a meal with a full glass of water or according to your doctor's recommendations. Swallow the tab whole, do not chew, crush, or open the capsule as may destroy the drug and/or increase side effects. Antacids drugs can be taken together with this medicine, if necessary. Dosage and duration of treatment depends on your medical condition and response to the therapy. Take it the same time each day to avoid missing a dose. In the case of aggravation or worsening of your illness notify your doctor immediately. It may take 1 - 4 days before Prilosek acts in full measure. Treatment with Prilosec should not be stopped even if certain amelioration is achieved. Improvement of symptoms is observed within 4 to 8 weeks in treatment of gastric ulcers or reflux disease. Treatment of heartburn usually lasts for 14 days. If heartburn persists after this period of time or even worsens, or if you need more than one course of treatment every 4 months, contact your doctor or pharmacist.

Precautions Prilosec is not recommended during pregnancy. Breastfeeding when using this drug is not recommended as it is not known whether it gets into breast milk. Tell your doctor if allergic reaction appears. Your doctor or pharmacist should be aware of your health problems, to provide health care, especially if you have problems such as liver disease, other stomach problems (e. g. tumors), heartburn over 3 months, unexplained weight loss, constant nausea/vomiting /stomach pain, blood in vomit or black stools. Some symptoms may witness about a more serious condition. This medicine may cause dizziness. Be careful performing work associated with concentration of attention, such as driving or operating mechanisms. Restrict consumption of alcoholic beverages. Start or interruption in taking any medicine should be be approved by your doctor. If you do not notice any improvement of your symptoms or if they even become worse, inform your doctor about it. Do not share this medicine with anybody with similar symptoms. Do not use this medicine to treat other diseases.

Possible side effects Adverse reactions that may disappear during treatment include headache, constipation, cough, dizziness, or rash. If they continue or are bothersome, let your doctor know about it. An allergic reaction to this medicine is not expected, but seek immediate medical help if it happens. Symptoms of an allergic reaction appear as rash, itching, dizziness, swelling, or difficult breathing. If you notice other reactions of your body which are not listed above, contact your doctor or pharmacist.

Prilosec can decreases elimination of diazepam, warfarin and phenytoin. These are medications metabolized in the liver by oxidation. Drugs which are metabolized with help of cytochrome P-450 system (e. g. cyclosporine, disulfiram, benzodiazepines) may also interact with Prilosec because it is metabolized the same way. Clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with Prilosec may result in increases in plasma levels of Prilosec. Concomitant use of Prilosec and clarithromycin may result in increases in plasma levels of erithromycin, and 14-hydroxy-clarithromycin. You may need additional monitoring of your condition if you are taking ampicillin, cilostazol, cyclosporine, diazepam, digoxin, disulfiram, iron, itraconazole, ketoconazole, moclobemide, phenytoin, sucralfate, vorconizole, or warfarin. This medicine may be combined with antacids if they were prescribed by your doctor. Potent acid-reducing drugs such as Prilosec diminish the effectiveness of sucralfate, and other medicaitons such as the antifungals ketoconazole and itraconazole. If instructed to take any of these medicines while taking Prilosec, consult your doctor or pharmacist regarding the proper timing of each dose, usually Prilosec is taken 30 minutes before sucralfate.

Missed dose If you missed a dose take the medication as soon as you remember. If it is almost time of your next dose, just skip its intake and return to your regular schedule.

Overdose If suppose that took too much of Prilosec contact your local poison control center or emergency room immediately. Symptoms of overdose are confusion, blurred vision, unusual sweating, or unusually fast heartbeat.

Storage Store at room temperature between 59-77 F (15-25 C). Do not expose to high humidity or keep in a bathroom. Hide Prilosec away from children and pets. If your treatment requires an extended period of time, take care about refills before your supply is over.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Buy Lowcholid Ezetimibe Simvastatin Online Without Prescriptions, Lowcholid

Vytorin is used for treating high cholesterol along with a cholesterol-lowering diet. Vytorin is a combination of 2 medicines. Ezetimibe works by reducing the amount of cholesterol that your body absorbs from your diet. Simvastatin is an HMG-CoA reductase inhibitor or "statin." It works by blocking an enzyme that is necessary for your body to make cholesterol. Lowering cholesterol levels in the blood reduces the chance of heart disease, heart attacks, and strokes. Vytorin has not been shown to reduce heart attacks or strokes more than simvastatin alone.

Use Vytorin as directed by your doctor.

Take Vytorin by mouth with or without food, preferably in the evening, unless directed otherwise by your doctor.

Taking Vytorin at the same time each day will help you remember to take it.

If you also take a bile acid sequestrant (eg, cholestyramine, colestipol, colesevelam), do not take it within 2 hours before or 4 hours after taking Vytorin. Check with your doctor if you have questions.

For best results, Vytorin should be used along with exercise, a low-cholesterol/low-fat diet, and a weight-loss program if you are overweight. Follow the diet and exercise program given to you by your health care provider.

Eating grapefruit or drinking grapefruit juice may increase the amount of Vytorin in your blood, which may increase your risk for serious side effects. The risk may be greater with large amounts of grapefruit or grapefruit juice. Avoid large amounts of grapefruit or grapefruit juice (eg, more than one quart daily). Talk with your doctor or pharmacist if you have questions about including grapefruit or grapefruit juice in your diet while you are taking Vytorin.

Most people with high cholesterol do not feel sick. Continue to take Vytorin even if you feel well. Do not miss any doses.

If you miss a dose of Vytorin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Vytorin.

Store Vytorin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Vytorin out of the reach of children and away from pets.

Active Ingredients: Ezetimibe, Simvastatin.

Do NOT use Vytorin if:

you are allergic to any ingredient in Vytorin

you have liver problems or ongoing abnormal liver function test results

you are taking another medicine that contains simvastatin or ezetimibe

you are taking an HIV protease inhibitor (eg, nelfinavir, lopinavir, ritonavir), itraconazole, ketoconazole, a macrolide or ketolide antibiotic (eg, clarithromycin, erythromycin, troleandomycin), mibefradil, or nefazodone

you are pregnant or breast-feeding.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Vytorin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you are a woman of childbearing age

if you have kidney problems, muscle problems, or a family history of muscle problems; low blood pressure; uncontrolled seizures; or serious metabolic, endocrine, or electrolyte problems

if you are scheduled for major surgery, have recently had a major trauma, or have a severe infection or history of alcohol abuse

if you have had an organ transplant and are taking medicine to suppress a rejection reaction.

Some medicines may interact with Vytorin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Amiodarone, angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), azole antifungals (eg, itraconazole, ketoconazole), cyclosporine, danazol, delavirdine, diltiazem, fibrates (eg, clofibrate, fenofibrate), fluconazole, gemfibrozil, HIV protease inhibitors (eg, ritonavir), imatinib, macrolide antibiotics (eg, erythromycin), macrolide immunosuppressives (eg, tacrolimus), mibefradil, nefazodone, niacin, nicotinic acid, streptogramins, telithromycin, verapamil, or voriconazole because side effects, such as muscle pain, may occur

Bosentan, carbamazepine, cholestyramine, hydantoins (eg, phenytoin), rifampin, or St. John's wort because they may decrease Vytorin's effectiveness

Anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Vytorin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Vytorin 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.

Important safety information:

Vytorin may cause dizziness, drowsiness, or changes in vision. These effects may be worse if you take it with alcohol or certain medicines. Use Vytorin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

It may take several weeks for Vytorin to work.

Proper dental care is important while you are taking Vytorin. Brush and floss your teeth and visit the dentist regularly.

Vytorin may harm your liver. Your risk may be greater if you drink alcohol while you are using Vytorin. Talk to your doctor before you take Vytorin or other fever reducers if you drink more than 3 drinks with alcohol per day.

Vytorin may cause injury to your muscles, especially when taken at higher doses or when taken with certain other medicines. Contact your doctor right away if you experience muscle pain, tenderness, or weakness, especially with a fever.

Some patients taking Vytorin have reported poor memory or trouble sleeping. If you experience these effects, check with your doctor.

Lab tests, including blood cholesterol levels, liver function tests, or muscle tests, may be performed while you use Vytorin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Vytorin should be used with extreme caution in children younger 10 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Do not use Vytorin if you are pregnant. Avoid becoming pregnant while you are taking it. If you think you may be pregnant, contact your doctor right away. It is not known if Vytorin is found in breast milk. Do not breastfeed while taking Vytorin.

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:

Diarrhea; flu-like symptoms; headache; pain in the arms or legs; tiredness; upper respiratory tract infection.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing or swallowing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision or vision changes; change in the amount of urine; chest pain; dark urine; depression; fast heartbeat; fever; loss of appetite; muscle tenderness, pain, or weakness; nausea; numbness, tingling, burning, or weakness in the arms, hands, feet, or legs; pale stools; stomach tenderness; unexplained pain in the stomach or mid-upper back; unusual bruising or bleeding; unusual tiredness; vomiting; yellowing of the skin or eyes.

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.

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Mebex - Anti-Anxiety Agents, Anticonvulsants, Hypnotics And Sedatives, Muscle Relaxants, Central, At

Mebex

Tablet for oral administration (200 mg, 400 mg)

Mebex Indication

For the management of anxiety disorders or for the short-term relief of the symptoms of anxiety.

Mebex Pharmacology

Meprobamate is an anxiolytic drug. It was the best selling minor tranquilizer for a time but has largely been replaced by benzodiazepines. Meprobamate has most of the pharmacological effects and dangers of the barbiturates (though it was marketed as being safer). However, it is less sedating at effective doses. It is reported to have some anticonvulsant properties against absence seizures, but can exacerbate generalized tonic-clonic seizures. It has also been used as a hypnotic (sleeping pill). However, its is currently only licensed as an anxiolytic and it is a third or fourth-order choice.

Mebex Absorption

Well absorbed from the gastrointestinal tract.

Mebex side effects and Toxicity

Symptoms of overdose include coma, drowsiness, loss of muscle control, severely impaired breathing, shock, sluggishness, and unresponsiveness. Death has been reported with ingestion of as little as 12 g meprobamate and survival with as much as 40 g.

Mebex Patient Information

Mebex Organisms Affected

Humans and other mammals

Bula Do Medicamento Busonid Caps, Busonid

Budesonida 200mcg e 400mcg Capsulas

FORMA FARMACEUTICA E APRESENTACOES: - BUSONID CAPS Embalagem com 60 capsulas contendobudesonida 200 mcg e 400 mcg em po para inalacao e 1 inalador. Embalagem com 60 capsulas contendo budesonida 200 mcg e 400 mcg em po para inalacao (refil).

USO ADULTO E PEDIATRICO USO INALATORIO ORAL

COMPOSICAO: - BUSONID CAPS Cada capsula com po para inalacao 200 mcg contem: Budesonida. 200 mcg Excipiente: lactose. Cada capsula com po para inalacao 400 mcg contem: Budesonida. 400 mcg Excipiente: lactose.

INFORMACOES AO PACIENTE: - BUSONID CAPS Acao esperada do medicamento: BUSONIDCAPS (Budesonida) capsulas e indicado como tratamento preventivo das doencas pulmonares obstrutivas, reduzindo a inflamacao2 nos bronquios. Nao possui indicacao nas crises agudas. Cuidados de armazenamento: Conservar em temperatura ambiente (entre 15 e 30oC) e proteger da umidade. Prazo de validade: O produto possui prazo de validade de 18 meses. Nao utilizar o medicamento com o prazo de validade vencido. Gravidez1 e lactacao3: Informar ao seu medico a ocorrencia de gravidez1 na vigencia do tratamento. Cuidados de administracao: Para assegurar uma administracao adequada, o paciente deve ser informado sobre as instrucoes de uso do inalador pelo medico ou por outro profissional da saude. E importante para o paciente entender que a capsula de gelatina pode fragmentar - se e que pequenos pedacos de gelatina podem atingir a boca ou a garganta apos a inalacao. As capsulas so devem ser retiradas do blister imediatamente antes do uso. Siga a orientacao de seu medico, respeitando sempre os horarios, as doses e a duracao do tratamento. ATENCAO: NAO ENGULA AS CAPSULAS, USE EXCLUSIVAMENTE PARA INALACAO. Interrupcao do tratamento: Nao interromper o tratamento sem o conhecimento do seu medico. A eficacia de seu tratamento depende do uso regular dessa medicacao. E IMPORTANTE QUE VOCE MANTENHA A MEDICACAO PRESCRITA, NAO INTERROMPENDO OU REDUZINDO AS DOSES, MESMO QUE VOCE ESTEJA SE SENTINDO BEM. Reacoes adversas: Informe seu medico sobre o aparecimento de reacoes desagradaveis. Podem ocorrer irritacao na garganta, tosse e rouquidao. Tambem pode ocorrer infeccao4 na garganta e alteracoes oculares. TODO MEDICAMENTO DEVE SER MANTIDO FORA DO ALCANCE DAS CRIANCAS. Ingestao concomitante com outras substancias: Informe seu medico sobre qualquer medicamento que esteja usando, antes ou durante o tratamento. Comunique ao seu medico caso necessite utilizar qualquer outro tipo de medicamento. Contra - indicacoes e precaucoes: O produto nao deve ser administrado a pacientes sensiveis a budesonida ou a outros componentes da formula. Para o seu devido uso, procure entender perfeitamente as instrucoes que estao detalhadas anexas. Apos a inalacao do produto, enxague a boca com agua para evitar o aparecimento de candidiase5 (sapinho). Informe ao seu medico caso voce tenha tuberculose6 ou outras infeccoes respiratorias. Nao foram relatados casos de efeitos sobre a habilidade de dirigir e/ou operar maquinas. NAO TOME REMEDIO SEM O CONHECIMENTO DO SEU MEDICO, PODE SER PERIGOSO PARA A SAUDE.

INFORMACOES TECNICAS: - BUSONID CAPS MODO DE ACAO BUSONID CAPS (Budesonida) capsulas contem em sua formula um unico principio ativo, a budesonida, um glicocorticoide nao halogenado de sintese, cuja principal propriedade consiste em sua elevada acao antiinflamatoria local e atividade sistemica muito baixa, agindo de maneira profilatica no processo inflamatorio. Quando utilizado como po inalante, aumenta o deposito pulmonar da medicacao e reduz a acao sistemica quando comparado ao spray. Budesonida possui varios mecanismos que bloqueiam a atividade inflamatoria, como: a) inibicao da formacao de anticorpos7 especificos; b) prevencao da formacao, armazenamento, liberacao e ativacao de mediadores quimicos da inflamacao2, como cininas, histaminas, prostaglandinas, enzimas lipossomais e leucotrienos; c) interferencia no broncospasmo, no edema8 inflamatorio e tambem na secrecao glandular; d) inibicao da marginacao e migracao celular, alem de reverter a dilatacao e diminuir a permeabilidade vascular9 no sitio inflamatorio e outros mecanismos ainda nao especificados.

INDICACOES: - BUSONID CAPS Tratamento profilatico de broncopatias cronicascom definido componente inflamatorio, como a asma10 bronquica, produzindo alivio dos sintomas11 e prevencao da deterioracao da funcao pulmonar.

CONTRA-INDICACOES: - BUSONID CAPS O produto nao deve ser administrado aos pacientes sensiveis a budesonida ou a qualquer outro componente da formula, em mal asmatico ou outros episodios agudos de asma10.

PRECAUCOES: - BUSONID CAPS Na transferencia da terapia oral paratopica com BUSONID CAPS (Budesonida) capsulas, observar atentamente enquanto ocorre a reducao da dose de corticoide oral em relacao a possiveis sintomas11 de insuficiencia12 adrenal. Deve - se evitar a substituicao da corticoterapia oral para topica durante situacoes de "stress", como cirurgias, infeccoes e traumas. Alguns pacientes apresentam sintomas11 de retirada de corticoide quando ha a transferencia da corticoterapia oral para topica. Na presenca de broncospasmo paradoxal, deve - se suspender a medicacao e instituir tratamento broncodilatador13. Podem ocorrer aumento da pressao intra - ocular, glaucoma14 ou catarata15. Criancas podem absorver proporcionalmente maiores quantidades da medicacao e estao mais suscetiveis a toxicidade sistemica. A corticoterapia pode reduzir o crescimento em criancas, portanto, devem utilizar a menor dose efetiva; deve - se monitorar a taxa de crescimento rotineiramente. A corticoterapia pode aumentar o risco de desenvolvimento de infeccoes graves ou fatais em individuos expostos a doencas virais, como varicela16 e sarampo17. Deve - se monitorar rigorosamente pacientes com tuberculose6 ativa ou quiescente, infeccoes bacterianas, fungicas refratarias, virais sistemicas e herpes simples ocular. As regioes axilares e inguinais estao propensas ao desenvolvimento de estrias. Em caso de irritacao local apos o uso da medicacao, o produto pode ser descontinuado e instituir agentes antimicrobianos se houver infeccao4 secundaria. Se, entretanto, uma infeccao4 viral das vias respiratorias superiores esta presente, o paciente deve receber medicacao antiasmatica regular. Em pacientes, os quais sabidamente pioram rapidamente quando apresentam infeccao4 respiratoria viral, deve - se considerar tratamento de curto periodo com corticosteroides orais. Os estudos clinicos mostram que as infeccoes virais causam problemas menos significantes quando o paciente esta sob tratamento regular com glicocorticosteroides topicos. Pacientes que fazem uso a longo prazo de corticoterapia devem ser observados quanto a supressao do eixo hipotalamoadrenal (HPA). O tratamento com BUSONID CAPS (Budesonida) capsulas nao deve ser interrompido abruptamente, devido a possibilidade de ocorrer insuficiencia12 da supra - renal18.

GRAVIDEZ1 E LACTACAO3: - BUSONID CAPS Classificado como categoria "C" pelo FDA: BUSONID CAPS (Budesonida) capsulas so deve ser usado durante a gravidez1 se os beneficios justificarem os riscos em potencial para o feto. Somente o medico deve determinar o uso do medicamento durante o periodo de gravidez1. Os bebes19, de maes em tratamento durante a gravidez1, podem apresentar hipoadrenalismo, ao nascer. Os estudos em animais tem demonstrado que os corticosteroides podem produzir varios tipos de malformacoes fetais, apesar de tais efeitos nao serem confirmados para a especie humana. BULA BUSONID CAPS Formato: 150 x 210 mm Cor: Black Modelo de bula: 2bsnca3 Codigo: 5528 5528 Importado e distribuido por: LABORATORIOS BIOSINTETICA LTDA. Av. das Nacoes Unidas, 22.428 Sao Paulo - SP CNPJ n? 53.162.095/0001- 06 Industria Brasileira Atendimento ao Consumidor: 0800- 15-1036 Cod. Laetus n? 93 Se o tratamento com glicocorticoides durante a gravidez1 for inevitavel, devese dar preferencia ao uso inalatorio, tendo em vista seu efeito sistemico menor, comparado com equipotentes doses orais. O aleitamento materno20 e seguro.

INTERACOES MEDICAMENTOSAS: - BUSONID CAPS A cinetica de budesonida foi investigadaem individuos sadios com e sem administracao de cimetidina (dose 1.000 mg/dia). Apos a dose oral de 4 mg de budesonida, os valores para concentracao maxima (nmol/l) e a disponibilidade sistemica (%) com e sem cimetidina (3,3 x 5,1 nmol/l e 10 x 12%, respectivamente) indicaram que a cimetidina causou um leve efeito inibitorio no metabolismo21 hepatico da budesonida, o qual deve ser de pouca importancia clinica.

REACOES ADVERSAS: - BUSONID CAPS As reacoes adversas mais frequentemente comunicadas sao: boca seca, disfonia22, irritacao na garganta, dor de garganta e infeccao4 por candida na cavidade bucal, laringe23 e faringe24. Ocasionalmente podem ocorrer espirros e uma ligeira secrecao hemorragica nasal e catarata15 subcapsular. Raramente podem ocorrer: supressao da funcao hipotalamica - pituitaria-adrenal, reacao de hipersensibilidade, incluindo urticaria25, angioedema26, rash27 cutaneo e broncoespasmo28 imediato em pacientes hipersensiveis, que devera ser tratada administrando - se um beta-2 adrenergico de curta duracao por inalacao. Alguns estudos realizados demonstraram diferentes resultados sobre o retardo do crescimento pondero - estatural, sendo necessario a observacao de estudos a longo prazo para obtermos esta resposta. Foram relatados casos de sintomas11 psiquiatricos tais como nervosismo, agitacao e depressao, bem como alteracoes comportamentais em criancas.

POSOLOGIA: - BUSONID CAPS Na deflagracao da capsula, a quantidade debudesonida que e liberada e o equivalente a quantidade de medicacao contida na capsula. A posologia deve ser individualizada. O beneficio maximo da budesonida e obtido em 3 a 7 dias de tratamento. O produto nao esta destinado a obter um alivio rapido, mas sim duradouro, e, portanto, deve - se fazer uso prolongado da medicacao. Quando o efeito desejado for obtido, a dose de manutencao pode ser reduzida para a menor dose necessaria ao controle terapeutico. Criancas maiores de 6 anos: a dose usual e de 200 a 800 mcg em dose unica, que pode ser dividida em 2 doses diarias, ou entao aumentada, caso haja falta de controle clinico, para 400 mcg a 1.000 mcg 2 vezes ao dia. Criancas maiores de 12 anos e adultos: a dose usual e de 400 a 800 mcg em dose unica, que pode ser dividida em 2 doses diarias, ou entao aumentada, caso haja falta de controle clinico, para 800 mcg 2 vezes ao dia. Criancas menores de 5 anos: a dose recomendada e de 100 a 400 mcg 2 vezes ao dia, podendo ser aumentada ate 2.000 mcg ao dia*. Cabe ao medico decidir a idade minima para iniciar o tratamento com BUSONID CAPS (Budesonida), ja que as apresentacoes em po seco sao iniciadas a partir dos 6 anos de idade (devido ao baixo fluxo inalatorio). * Dose segundo Consenso Britanico para o Manuseio da Asma10. O BUSONID CAPS (Budesonida) capsulas deve ser utilizado sob a supervisao de um adulto, pois a eficacia do tratamento depende da habilidade da crianca em utilizar o inalador corretamente. Nao e necessario o ajuste de dose em idosos ou em nefropatas e hepatopatas.

SUPERDOSE: - BUSONID CAPS A sua baixa atividade sistemica faz com que o risco de intoxicacao com BUSONID CAPS (Budesonida) capsulas seja muito improvavel. De qualquer forma, a interrupcao do tratamento seria suficiente para fazer desaparecer os sintomas11 de intoxicacao. Se, em alguma circunstancia especial, aparecerem sintomas11 de hipercorticismo (edema8, cara de lua cheia), corrigir o desequilibrio eletrolitico com diureticos29 que nao afetem o potassio, tais como: o espironolactona e o triantereno.

USO EM IDOSOS: - BUSONID CAPS Apesar de nao haver estudos adequados com corticoides na populacao geriatrica, nao sao esperadas que as alteracoes comuns desta faixa etaria limitem o beneficio maximo deste tipo de medicamento, desde que sejam respeitadas as suas precaucoes. Nao se faz necessario reajuste de dose para esta populacao. VENDA SOB PRESCRICAO MEDICA MS - 1.1213.0173 Resp. Tecn. Farm. Luiz A. M. Mendes CRF - SP n? 13559 N? lote, data de fabricacao e validade: vide cartucho. Fabricado por: LICONSA - Espanha

BUSONID CAPS - Laboratorio

Condylox Topical Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Conebilox

Condylox topical

Uses

How to use Condylox topical

This medication is for topical use only. Apply it on the warts pointed out by your doctor. It is usually applied once in the morning and again in the evening for 3 days followed by a 4 day rest period. If the warts do not go away, then this cycle is repeated up to 4 times. Contact your doctor for other options if the warts do not go away after 4 weeks of treatment.

To apply, use the provided applicator tip or your finger. Apply a small amount of medication to the wart to cover it. Allow the gel to dry. Wash your hands thoroughly afterwards. Be careful with this medication because it can irritate normal skin around the application site.

Do not use large amounts, apply more often or use for a longer period than directed. Your condition will not clear faster, and the chance for side effects may be increased.

Avoid contact with the eyes and mucous membranes. If contact occurs, immediately wash with plenty of water and contact your doctor.

Read the Patient Information Leaflet available from your pharmacist. Consult your doctor or pharmacist if you have any questions.

Side Effects

Swelling, pain, burning, itching. peeling skin, small sores, or headache may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Tell your doctor right away if this serious side effect occurs: bleeding.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking podofilox. tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: other skin problems (e. g. skin cancer ).

This medication must not be used during pregnancy. Women of child-bearing age should use a reliable form of birth control while using this medication. If you become pregnant or think you may be pregnant, inform your doctor right away.

It is unknown if this drug passes into breast milk. Consult your doctor before breast - feeding.

Interactions

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use.

Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. This medicine may be harmful if swallowed. If accidentally swallowed, you may experience symptoms such as: nausea. vomiting. diarrhea. change in mental status, weakness or fatigue. unusually slowed breathing, and seizures .

Notes

This medication is prescribed for your current condition only. Do not use it later for another skin problem unless directed by your doctor. A different medication may be necessary in those cases.

Do not share this medication with others.

This medication is not a cure. New warts or return of old warts may occur, especially in the first 3 months after treatment. Follow-up medical visits may be periodically necessary to monitor your progress or check for side effects. Consult your doctor for more details.

Refrain from sexual intercourse on the days you apply this drug. Using condoms may help prevent the spread of genital warts to your partner.

Missed Dose

If you miss a dose, apply it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature between 59-86 degrees F (15-30 degrees C) away from heat or open flame. Do not freeze. Replace the cap tightly after use. Do not store in the bathroom. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

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Order Medication Online Antibiotics, Pain Relief, Skin Care, Nitroretard Faran

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Tilhasan 60 - Thu?c Di?u Tr? Dau Th?t Ng?c - Thong Tin B?nh Vi?n, Tilhasan

Con dau th?t ng?c, dau th?t ng?c ki?u Prinzmetal 60 mg x 3 l?n/ngay ho?c 30 mg x 4 l?n/ngay, tang li?u khi c?n trong 1-2 ngay sau.

Tang huy?t ap vo can 30-60 mg x 3 l?n/ngay, co th? ph?i h?p v?i thu?c tr? tang HA khac.

Ngu?i cao tu?i, suy gan, th?n: gi?m li?u.

Khong tang li?u khi nh?p tim < 50 l?n/phut.

Co th? dung luc doi ho?c no

U?ng v?i nhi?u nu?c, nu?t nguyen vien, khong nhai.

M?n c?m v?i b?t c? thanh ph?n nao c?a thu?c

R?i lo?n ho?t d?ng nut xoang.

Nh?p tim < 40 l?n/phut.

Bl?c nhi th?t d? II, III khong d?t may t?o nh?p.

Suy th?t trai kem sung huy?t ph?i, nh?i mau co tim c?p.

Co thai/cho con bu.

B?nh nhan bl?c nhi th?t d? I ho?c PR keo dai, ch?m nh?p tim, suy tam th?t tru?c do.

Huy?t ap tam thu < 90 mmHg.

Dai thao du?ng.

B?nh nhan l?n tu?i, suy th?n, suy gan.

Khi gay me.

Lai xe/v?n hanh may.

Phu chi du?i, chong m?t, m?t m?i, suy nhu?c, m?t ng?, bu?n non, ch?m nh?p tim, bl?c nhi th?t c?p d? I, ho, d? ?ng

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Trinh bay va dong goi:

Vien nen bao film: 60 mg x 3 v? x 10 vien

Gia ban: Dang c?p nh?t

Magnolias Cakery, Maganol

Welcome to Magnolias Cakery, where we make "Edible Art Creations" out of cake!

I have been making cakes for the last 12 years for my three children, friends and other family members. A few years ago I had been asked to make cakes for friends of friends, co-works, and more! So I decided that it was time to make a living out of a much loved hobby!

I have a cute little shop in Hortonville, WI where you are able to stop in and grab your choice of sweet treats! We currently offer cupcakes, cake pops, cheesecake slices, cake slices and cookies. Our flavors are always changing so be sure to stop or follow us on facebook to see what flavors we are running! Or stop in to place an order!

I have an associates degree in interior design and have always loved art and creating things with my hands. So naturally I put my knowledge and love into each cake that I create and I try to make it personal to each and every client.

All of my cake recipes are made from scratch, resulting in wonderful flavors and the best moist cakes you have ever had! I try to make everything I put on my cakes edible.

I create cakes for all occasions, weddings, birthdays, showers, anniversary's, christenings, graduations, seasonal and any other reason to eat cake! Just remember cake travels!

I hope I can make your next event special with cake!

Heidi Hoewisch owner/cake artist (920)427-3829

204 W. Main Street, Hortonville, WI 54944

Emitac Reviews, Omitac

Emitac Reviews

Have heard form my other colleagues when they left the organization that they have not been paid there exact dues, now am experiencing the same for myself. Emitac management is highly biased towards one nationality specially in Abu Dhabi branch and they don't take good care of the employees although we have worked there day and night.

They are getting very bad image in the market because of their unsatisfied ex employees, they are not embracing diversity and don't have respect for their employees, management can shout and use abusive language with their employees and no one dares to raise the voice as if he will do so it will cost him his job.

Advice to Management

Should treat there employees with respect even if they have left the organization, and try to settle their dues in a proper respectful way, open their eyes and understand that we are living in the computer age not in the stone age.

Ronaxan, Ronaxan

Ronaxan Tablets for Dogs & Cats

You will receive VioPoints by purchasing this product, which can be redeemed for a discount on future purchases. For each 1000 points redeemed at the checkout, you will receive a 20p discount. Ts & Cs apply.

We will need a valid prescription from your vet before we can dispatch an order for this item. Information

Product Details

Ronaxan Tablets contain the antibiotic doxycycline and are used in cats and dogs. The spectrum of activity of Ronaxan makes it particularly suitable for respiratory infections and so it is usually used for rhinitis, sinusitis, tonsilitis and broncho-pneumonia. Doxycycline is more fat soluble than many other antibiotics and penetrates tissues well, so it is sometimes prescribed for other infections, such as prostatitis in male dogs. Ronaxan Tablets are normally given once daily with a meal for 5 days.

Presentation

Round, yellow tablets each containing 20 mg or 100 mg doxycycline, as doxycycline hyclate.

20 mg tablets are indicated for use in both cats and dogs, 100 mg tablets are indicated for use in dogs only.

Uses

For the treatment of respiratory tract infections in cats and dogs, including rhinitis, tonsillitis, bronchopneumonia and feline respiratory disease. The therapeutic spectrum includes Pasteurella spp. Bordetella bronchiseptica, Staphylococcus aureus, other Staphylococcus spp. and Streptococcus spp.

Dosage and administration

The tablets are for oral administration. The dosage is 10 mg per kg bodyweight (one 20 mg tablet per 2 kg or one 100 mg tablet per 10 kg) administered daily for up to five days.

Tablets should be administered at feeding times.

Contra-indications, warnings, etc

For animal treatment only.

Do not exceed the recommended dosage.

RONAXAN should not be used in pregnant animals.

Do not use in known cases of hypersensitivity to the active ingredient.

Vomiting, oesophagitis and oesophageal ulcerations have been reported as side effects following doxycycline therapy and RONAXAN should not therefore be administered to patients with dysphagia, or diseases accompanied by vomiting.

Photodermatitis has occurred following tetracycline therapy after exposure to intense sun or ultraviolet light.

The use of tetracycline during tooth development may lead to tooth discoloration. Doxycycline, because of the lower affinity for calcium, carries a lower risk than other tetracyclines.

Cross resistance to other tetracyclines can occur.

Doxycycline should not be used concurrently with other antibiotics especially bactericidal drugs such as the β-lactams.

Wash hands thoroughly after use.

Handle the tablets with care if you know you are hypersensitive (allergic) to tetracycline. In case of accidental ingestion, seek medical advice.

Container disposal

Any unused product or waste material should be disposed of in accordance with national requirements.

Pharmaceutical precautions

Avonex (Interferon Beta-1a) Side Effects, Interactions, Warning, Dosage & Uses, Ivenox

DRUG DESCRIPTION

AVONEX is a 166 amino acid glycoprotein with a molecular weight of approximately 22,500 daltons. It is produced by recombinant DNA technology using genetically engineered Chinese Hamster Ovary cells into which the human interferon beta gene has been introduced. The amino acid sequence of AVONEX is identical to that of natural human interferon beta.

Using the World Health Organization (WHO) International Standard for Interferon, AVONEX has a specific activity of approximately 200 million international units of antiviral activity per mg of interferon beta-1a determined specifically by an in vitro cytopathic effect bioassay using lung carcinoma cells (A549) and Encephalomyocarditis virus (ECM). AVONEX 30 micrograms contains approximately 6 million international units of antiviral activity using this method. The activity against other standards is not known. Comparison of the activity of AVONEX with other interferon betas is not appropriate, because of differences in the reference standards and assays used to measure activity.

AVONEX Lyophilized Powder Vial

A vial of AVONEX is a sterile, white to off-white lyophilized powder for intramuscular injection after reconstitution with supplied diluent (Sterile Water for Injection, USP). Each vial of reconstituted AVONEX contains 30 micrograms of interferon beta-1a; 15 mg Albumin (Human), USP; 5.8 mg Sodium Chloride, USP; 5.7 mg Dibasic Sodium Phosphate, USP; and 1.2 mg Monobasic Sodium Phosphate, USP, in 1.0 mL at a pH of approximately 7.3.

AVONEX Single-Use Prefilled Syringe

A prefilled syringe of AVONEX is a sterile liquid for intramuscular injection. Each 0.5 Ml (30 microgram dose) of AVONEX in a prefilled glass syringe contains 30 micrograms of interferon beta-1a, 0.79 mg Sodium Acetate Trihydrate, USP; 0.25 mg Glacial Acetic Acid. USP; 15.8 mg Arginine Hydrochloride, USP; and 0.025 mg Polysorbate 20 in Water for Injection, USP at a pH of approximately 4.8.

AVONEX PEN Single-Use Prefilled Autoinjector

AVONEX PEN is a sterile liquid for intramuscular injection in a prefilled glass syringe surrounded by an autoinjector. Each 0.5 mL (30 microgram dose) in the AVONEX PEN contains 30 micrograms of interferon beta-1a, 0.79 mg Sodium Acetate Trihydrate, USP; 0.25 mg Glacial Acetic Acid, USP; 15.8 mg Arginine Hydrochloride, USP; and 0.025 mg Polysorbate 20 in Water for Injection, USP at a pH of approximately 4.8.

What are the possible side effects of interferon beta-1a (Avonex, Avonex Prefilled Syringe, Rebif)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have a serious side effect such as:

depressed mood, anxiety, trouble sleeping, restlessness, or thoughts of suicide or hurting yourself;

easy bruising or bleeding, weakness;

seizure (convulsions);

numbness or tingling in your hands or feet;

pain or burning when you urinate;

pain, swelling, or skin.

What are the precautions when taking interferon beta-1a (Avonex)?

Before using interferon, tell your doctor or pharmacist if you are allergic to it; or to products containing human albumin; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

There is a risk of contracting a virus from using this medication because it contains albumin from human blood. Careful screening of blood donors, special manufacturing methods, and FDA-approved tests are all used to reduce such a risk. For more details, talk to your doctor.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: mental/mood disorders (e. g. depression, psychosis, suicidal thoughts), heart disease (e. g. angina.

Last reviewed on RxList: 5/5/2016 This monograph has been modified to include the generic and brand name in many instances.

Used Mercedes Benz For Sale, Carmaz

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Levlen - Woman S Health, Levonorgestrelum

Levlen is used for preventing pregnancy. Levlen is a combination birth control pill. It works by preventing ovulation, altering the cervical mucus, and changing the lining of the uterus.

Use Levlen as directed by your doctor. Take Levlen by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Begin taking Levlen on the first Sunday following the start of your period, unless otherwise directed by your doctor. If your period begins on a Sunday, begin taking Levlen on that day. Try to take Levlen at the same time every day, not more than 24 hours apart. After taking the last pill in the pack, start taking the first pill from a new pack the very next day. For Levlen to be effective it must be taken every day. Do not skip doses. If you miss a dose of Levlen and remember it on the same day, take it as soon as possible and go back to your regular dosing schedule. If you do not remember until the next day or if you miss more than 1 dose of Levlen, contact your doctor for further instructions. You may need to use an extra form of birth control (eg, condoms). If you are not sure about how to handle missed doses of Levlen, use an extra form of birth control (eg, condoms) until you talk with your doctor.

Ask your health care provider any questions you may have about how to use Levlen.

Store Levlen at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Levlen out of the reach of children and away from pets.

Active Ingredients: Levonorgestrel and Ethinyl Estradiol.

Do NOT use Levlen if: you are allergic to any ingredient in Levlen you are pregnant or think you may be pregnant you have a history of blood clotting problems, severe blood clots (eg, in the lungs, legs, eyes), certain blood vessel problems (eg, bleeding in the brain, heart attack, stroke), or breast cancer you are at risk for developing severe blood clots or have certain heart problems (eg, certain heart valve problems, certain types of irregular heartbeat) you have chest pain caused by angina; certain types of headaches or migraines with aura; severe or uncontrolled high blood pressure; endometrial, cervical, or vaginal cancer; estrogen-dependent growths; or undiagnosed abnormal vaginal bleeding; or diabetes that affects circulation you have liver disease, liver tumors or cancer, or a history of yellowing of the eyes or skin caused by pregnancy or prior birth control use you have had surgery and are or will be confined to a bed or a chair for an extended period of time you are older than 35 years old and you smoke 15 or more cigarettes per day.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Levlen. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have endometriosis, growths in the uterus, abnormal mammogram, irregular menstrual periods, a lump in the breast, heart problems, diabetes, headaches or migraines, gallbladder problems, high blood cholesterol or lipid levels, high blood pressure, kidney problems, blood problems (eg, porphyria), blood in the urine, depression or other mental/mood problems, lupus, chorea, high blood calcium levels, yellowing of the eyes or skin, pancreas problems (eg, pancreatitis), seizures (eg, epilepsy), or a history of cancer if you are overweight, you have not yet had your first menstrual period, or you use tobacco if you have given birth or otherwise ended a pregnancy within the past 4 weeks.

Some medicines may interact with Levlen. Tell your health care provider if you are taking any other medicines, especially any of the following: Atorvastatin, indinavir, or troleandomycin because they may increase the risk of Levlen's side effects Aprepitant, azole antifungals (eg, itraconazole, ketoconazole), barbiturates (eg, phenobarbital), bosentan, carbamazepine, dexamethasone, felbamate, griseofulvin, HIV protease inhibitors (eg, ritonavir), hydantoins (eg, phenytoin), modafinil, nevirapine, oxcarbazepine, penicillins (eg, amoxicillin), phenylbutazone, primidone, rifabutin, rifampin, St. John's wort, tetracyclines (eg, doxycycline), topiramate, or troglitazone because they may decrease Levlen's effectiveness, resulting in breakthrough bleeding or pregnancy Beta-blockers (eg, propranolol), corticosteroids (eg, prednisolone), cyclosporine, or theophylline because the risk of their side effects may be increased by Levlen Clofibric acid, lamotrigine, morphine, salicylic acid, or temazepam because their effectiveness may be decreased by Levlen.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Levlen 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.

Important safety information: Levlen may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Levlen with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Follow your doctor's instructions for examining your own breasts, and report any lumps immediately. If you will be having surgery or will be confined to a bed or chair for a long period of time (such as a long plane flight), notify your doctor 3 to 4 weeks ahead of time. Special precautions may need to be taken in these circumstances while taking Levlen. You should usually not take Levlen within 4 weeks after giving birth or otherwise ending a pregnancy. Discuss any questions or concerns with your doctor. Levlen may cause dark skin patches on your face. Exposure to the sun may make these patches darker. If patches develop, use a sunscreen or wear protective clothing when exposed to the sun, sunlamps, or tanning booths. Use of Levlen will not protect against HIV infection or prevent the spread of sexually transmitted diseases (STDs). Bleeding or spotting may occur while taking Levlen. Do not stop taking Levlen if this occurs. If bleeding or spotting continues for more than 7 days or is heavy, contact your doctor. Smoking while using Levlen may increase your risk of stroke, heart attack, blood clots, high blood pressure, or other diseases of the heart and blood vessels. Levlen may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using Levlen. Taking certain antibiotics, anticonvulsants, or other medicines, as listed in the interactions section, while you are using Levlen may decrease the effectiveness of Levlen. To prevent pregnancy, use an extra form of birth control (eg, condoms) until your next period. If you wear contact lenses and you develop problems with them, contact your doctor. If you miss your period during the week of inactive pills, call your doctor immediately. A missed period may indicate that you are pregnant. Levlen may take time to wear off after your last dose. You may not be able to become pregnant for several months after stopping Levlen. Discuss any concerns with your doctor or pharmacist. Lab tests, such as PAP tests, may be performed while you use Levlen. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Levlen should not be used in children who have not had their first menstrual period; safety and effectiveness in these children have not been confirmed. Pregnancy and breast-feeding: Do not use Levlen if you are pregnant. Avoid becoming pregnant while you are taking it. If you think you may be pregnant, contact your doctor right away. Levlen is found in breast milk. Do not breastfeed while taking Levlen.

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:

Acne; breast tenderness or enlargement; changes in appetite; changes in sexual interest; changes in weight; dizziness; hair loss; headache; nausea; stomach cramps or bloating; unusual spotting or bleeding; vomiting.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); breast discharge; breast lumps; calf or leg pain, swelling, or tenderness; change in amount of urine produced; change in vaginal secretions; changes in vision or speech; confusion; coughing of blood; crushing chest pain or heaviness in the chest; dark-colored urine; depression; difficulty sleeping; difficulty wearing contact lenses; fainting; fluid retention (swelling of the fingers and ankles); lack of energy; light-colored bowel movements; mental or mood changes; missed menstrual period; numbness of an arm or leg; one-sided weakness; persistent headache or migraines; persistent or recurrent abnormal vaginal bleeding; persistent or severe dizziness; severe pain or tenderness in the stomach; shortness of breath; sudden partial or complete loss of vision; sudden severe headache or vomiting; tiredness; vaginal irritation or discharge; weakness; yellowing of the skin or eyes.

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.

Buy Odacef (Cefixime) Without Prescription - Antibiotics, Odacef

Cefixime is used for treating attacks caused by certain bacterias. Cefixime can be a cephalosporin antibiotic. It functions by killing sensitive bacterias.

Make use of Cefixime as directed by your physician.

Take Cefixime orally with or without meals. If abdomen upset occurs, consider with food to lessen stomach irritation.

To get rid of your infection totally, continue using Cefixime for the entire program of treatment even though you feel much better in just a few days.

If you miss a dosage of Cefixime, take it as quickly as possible. If its almost time for the next dose, miss the missed dosage and get back to your regular dosing plan. Usually do not take 2 dosages at once.

Question your medical provider any questions you might have about how to make use of Cefixime.

Store Cefixime at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cefixime out of the reach of children and away from pets.

Do NOT use Cefixime if:

you are allergic to any ingredient in Cefixime or even to other cephalosporins (eg, cephalexin)

you will be having a live typhoid vaccine.

Contact your physician or doctor right away if these connect with you.

Some medical ailments may connect to Cefixime. Tell your physician or pharmacist when you have any medical conditions, particularly if the following connect with you:

if you are pregnant, likely to get pregnant, or are breast-feeding

if you are taking any prescription or non-prescription medicine, herbal preparation, or dietary supplement

if you possess allergies to medicines, foods, or other chemicals

if you experienced a severe allergic attack (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin (eg, amoxicillin) or beta-lactam antibiotic (eg, imipenem)

if you possess diarrhea, abdomen or bowel complications (eg, inflammation), bleeding or blood clotting complications, liver complications, or poor nourishment

if you have a brief history of kidney complications or you are on dialysis treatment.

Some medicines may connect to Cefixime. Tell your physician or pharmacist when you have any medical conditions, particularly if the following connect with you:

Anticoagulants (eg, warfarin) or carbamazepine as the risk of their unwanted effects could be increased by Cefixime

Live typhoid vaccines because their effectiveness could be reduced by Cefixime.

Ask your medical provider if Cefixime might interact with other drugs that you take. Consult with your health treatment provider before you begin, stop, or modification the dosage of any medication.

Essential safety information:

Cefixime could cause dizziness. This impact may be worse invest the it with alcoholic beverages or certain medicines. Make use of Cefixime with caution. Usually do not travel or perform other feasible unsafe jobs until you understand how you respond to it.

Do not change dosage forms (eg, tablets, suspension) of Cefixime without speaking together with your doctor.

Mild diarrhea is normal with antibiotic use. Nevertheless, a more serious type of diarrhea (pseudomembranous colitis) may rarely occur. This might develop while you utilize the antibiotic or within almost a year after you stop deploying it. Get in touch with your doctor immediately if stomach discomfort or cramps, serious diarrhea, or bloody stools happen. Do not deal with diarrhea without 1st checking together with your doctor.

Cefixime only functions against bacteria; it generally does not deal with viral infections (eg, the normal cold).

End up being sure to make use of Cefixime for the entire program of treatment. If you dont, the medicine might not get rid of your infection totally. The bacteria may possibly also become less delicate to the or other medications. This may make the disease harder to treat later on.

Long-term or repeated usage of Cefixime may trigger another infection. Tell your physician if signs of another infection occur. Your medication might need to be transformed to take care of this.

Cefixime may decrease the amount of clot-forming cells (platelets) in your bloodstream. Avoid activities that could cause bruising or damage. Tell your physician if you have uncommon bruising or bleeding. Inform your physician when you have dark, tarry, or bloody stools.

Do not get a live typhoid vaccine when you are acquiring Cefixime. It could not are well. Chat with your doctor in case you are scheduled to get a live typhoid vaccine.

Diabetes individuals - Cefixime could cause the outcomes of some recent tests for urine glucose or urine ketones to end up being wrong. Ask your physician before you modification your daily diet or the dosage of your diabetes medication.

Cefixime may hinder certain lab testing. Be sure your physician and lab staff know you are employing Cefixime.

Cefixime should be used in combination with extreme care in children younger six months; safety and performance in these children havent been confirmed.

Being pregnant and breast-feeding: In the event that you become pregnant, get in touch with your doctor. You will have to discuss the huge benefits and dangers of using Cefixime when you are pregnant. It isnt known if Cefixime is situated in breast milk. In case you are or will become breast-feeding when you use Cefixime, consult with your doctor or pharmacist. Discuss any feasible risks to your child.

All medicines may cause unwanted effects, but many folks have no, or small, side effects.

Check together with your doctor if these most common unwanted effects persist or become bothersome:

Diarrhea; gas; loose stools; nausea; stomach discomfort or upset.

Seek medical attention immediately if these severe unwanted effects occur:

Severe allergies (rash; hives; itching; problems breathing; tightness in the upper body; swelling of the mouth area, encounter, lips, or tongue; uncommon hoarseness); bloody stools; reduced urination; fever, chills, or sore throat; reddish colored, swollen, blistered, or peeling pores and skin; seizures; severe diarrhea; serious nausea / vomiting; severe stomach discomfort or cramping; uncommon bruising or bleeding; vaginal discharge or itching; white places in the mouth area; yellowing of your skin or eyes.

This isnt a complete set of all side effects that could occur. When you have queries about unwanted effects, contact your medical provider.

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Copyright © 2004-2016 All Rights Reserved

Colossal - Definition Of Colossal By The Free Dictionary, Closal

colossal

colossal

colossal

very big; enormous. a colossal increase in the price of books. kolos, reusagtig ?????? ????? колосален colossal obrovsky enorm kolossal; k?mpem?ssig ??????????? colosal hiiglasuur ???? ?????? ??? ???? jattilaismainen colossal ???? ????????, ???? ???? golem, divovski oriasi besar risastor colossale ??? ??? milziniskas kolosals; milzigs sangat besar kolossaal kolossal. kjempestor olbrzymi ???? ???? ?? astronomico colo­sal колоссальный ohromny ogromen gorostasan kolossal ????? cok buyuk. dev gibi ??? колосальний, величезний ??? ??? ? ???? kh?ng l? ???

Link to this page:

References in classic literature ?

It was a sight to see Queequeg seated over against Tashtego, opposing his filed teeth to the Indian's: crosswise to them, Daggoo seated on the floor, for a bench would have brought his hearse-plumed head to the low carlines; at every motion of his colossal limbs, making the low cabin framework to shake, as when an African elephant goes passenger in a ship.

He was one of the latter; and all outdoors, all life, was to him one colossal prison, which he paced like a pent-up tiger, trying one bar after another, and finding them all beyond his power.

I paused, and stood over that cowering lad a whole minute in awful silence; then, in a voice deep, measured, charged with doom, I began, and rose by dramatically graded stages to my colossal climax, which I delivered in as sublime and noble a way as ever I did such a thing in my life: "Go back and tell the king that at that hour I will smother the whole world in the dead blackness of midnight; I will blot out the sun, and he shall never shine again; the fruits of the earth shall rot for lack of light and warmth, and the peoples of the earth shall famish and die, to the last man

Excuse me, I see what a person of colossal ignorance and simplicity can do.

A long, lingering, colossal sigh followed, and his heart broke.

Throwing these into distance, rose, in the foreground, a head,--a colossal head, inclined towards the iceberg, and resting against it.

It opened into the house, where the females were already astir; Zillah urging flakes of flame up the chimney with a colossal bellows; and Mrs.

Over the door are my name, portrait, and autograph, expanded to colossal proportions, and surrounded in flowing letters, by the motto of the establishment, 'Down with the Doctors

Slowly the air grew dark, and we felt as if the earth was about to crumble away, and our fright was by no means diminished at seeing the genius, son of the daughter of Eblis, suddenly appear under the form of a colossal lion.

They have not erected to themselves colossal statues upon pedestals of human bones, to provoke and insult the tardy hand of heavenly retribution.

The bourgeoisie, during its rule of scarce one hundred years, has created more massive and more colossal productive forces than have all preceding generations together.

One, two--get out of the way," cried a colossal grenadier.

Veyxyl La 20% - Toko Sapibagustoko Sapibagus, Veyxyl

VEYXYL LA 20%

VEYXYL LA 20%

Product Description

Mengobati penyakit yang disebabkan oleh mikroorganisme Gram Positif dan Gram Negatif yang sensitif terhadap Amoxicillin. Infeksi paru-paru dan sistem pencernaan, infeksi dan urogenital, infeksi umum dan penyakit septicemia, infeksi bakteri, infeksi virus, erysipelas.

Sensitivitas terhadap patogen harus ditentukan melalui antibiogram sebelum menggunakan Veyxyl LA 20%. Karena tingkat perlawanan Amoxicillin yang sangat tinggi terhadap E. coli dan Salmonella, hal ini berlaku terutama untuk pengobatan infeksi pada saluran pencernaan.

Disuntik secara intramuskular pada Babi, Sapi, Domba, Anjing dan Kucing. Kocok dahulu sebelum digunakan. Pada Babi disuntik secara lateral muskular di bagian leher, untuk Sapi ke dalam elbow musculature. 0.5 ml / 10 Kg BB.

Jika tidak ada perubahan setelah 3 hari pengobatan, dapat dilakukan terapi lebih lama dengan sediaan ini. Setelah penurunan simptom klinikal, pengobatan dapat dilanjutkan selama 2 hari.

Info & Pemesanan: toko. sapibagus. com Komplek Rumah Pemotongan Hewan Tapos Jalan Tapos Raya, Depok. Jawa Barat 16457, Indonesia Email: sales@sapibagus. com Dian: 0821-2727-0221 Edy: 0816-966-247 Adi: 0811-1757-080

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Selo-Zok (Metoprolol) Report For Patients Like You, Selozok

Selo-Zok treatment report

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What is metoprolol?

Metoprolol is in a group of drugs called beta-blockers. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).

Metoprolol is used to treat angina (chest pain) and hypertension (high blood pressure). It is also used to treat or prevent heart attack.

Metoprolol may also be used for other purposes not listed in this medication guide.

Precautions

You should not use this medication if you are allergic to metoprolol, or if you have a serious heart problem such as heart block, sick sinus syndrome, or slow heart rate.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use this medication:

pheochromocytoma;

problems with circulation (such as Raynaud's syndrome);

congestive heart failure;

asthma, bronchitis, emphysema;

diabetes;

low blood pressure;

depression;

liver or kidney disease;

a thyroid disorder; or

myasthenia gravis.

FDA pregnancy category C. It is not known whether metoprolol is harmful to an unborn baby. Before taking this medication, tell your doctor if you are pregnant or plan to become pregnant during treatment.

Metoprolol can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Metoprolol can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Avoid drinking alcohol, which could increase drowsiness and dizziness while you are taking metoprolol.

Instructions

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include slow or uneven heartbeats, shortness of breath, bluish-colored fingernails, dizziness, weakness, or fainting.

Take the missed dose as soon as you remember. If your next dose is less than 4 hours away, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:

slow or uneven heartbeats;

feeling light-headed, fainting;

feeling short of breath, even with mild exertion;

swelling of your ankles or feet;

nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

depression; or

cold feeling in your hands and feet.

Less serious side effects may include:

vomiting;

decreased sex drive, impotence, or difficulty having an orgasm;

sleep problems (insomnia);

tired feeling; or

anxiety, nervousness.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Interactions

Before taking metoprolol, tell your doctor if you are using:

digoxin (digitalis, Lanoxin);

clonidine (Catapres);

ritonavir (Norvir);

terbinafine (Lamisil);

anti-malaria medications such as chloroquine (Aralen) or hydroxychloroquine (Plaquenil, Quineprox);

medicine to treat depression or mental illness, such as bupropion (Wellbutrin, Zyban), fluoxetine (Prozac, Sarafem), paroxetine (Paxil), thioridazine (Mellaril), and others;

an MAO inhibitor such as isocarboxazid (Marplan), tranylcypromine (Parnate), phenelzine (Nardil), or selegiline (Eldepryl, Emsam);

a diabetes medication such as insulin, glyburide (Diabeta, Micronase, Glynase), glipizide (Glucotrol), chlorpropamide (Diabinese), or metformin (Glucophage);

a heart medication such as nifedipine (Procardia, Adalat), quinidine (Quinaglute, Quinidex), propafenone (Rythmol), reserpine (Serpasil), verapamil (Calan, Verelan, Isoptin), diltiazem (Cartia, Cardizem);

medicine for asthma or other breathing disorders, such as albuterol (Ventolin, Proventil), bitolterol (Tornalate), metaproterenol (Alupent), pirbuterol (Maxair), terbutaline (Brethaire, Brethine, Bricanyl), and theophylline (Theo-Dur, Theolair);

a diuretic (water pill) such as amiloride (Midamor, Moduretic), chlorthalidone (Hygroton, Thalitone), furosemide (Lasix), hydrochlorothiazide (HCTZ, HydroDiuril, Hyzaar, Lopressor, Vasoretic, Zestoretic), spironolactone (Aldactazide, Aldactone), triamterene (Dyrenium, Maxzide, Dyazide), torsemide (Demadex), and others; or

cold medicines, stimulant medicines, or diet pills.

This list is not complete and there may be other drugs that can interact with metoprolol. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Other Names

Lopressor, Toprol-XL, metoprolol, and Metoprolol Succinate ER

Disclaimer

Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2004 Cerner Multum, Inc. Version 2.05. Revision date 8/23/04

Last updated: September 20, 2016

What is the most important information I should know about metoprolol?

You should not use this medication if you are allergic to metoprolol, or if you have a serious heart problem such as heart block, sick sinus syndrome, or slow heart rate.

Before taking metoprolol, tell your doctor if you have pheochromocytoma, circulation problems, congestive heart failure, asthma or other breathing problems, diabetes, low blood pressure, depression, liver or kidney disease, a thyroid disorder, or myasthenia gravis.

Metoprolol can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Avoid drinking alcohol, which could increase drowsiness and dizziness while you are taking metoprolol.

Do not stop taking metoprolol without first talking to your doctor. Stopping suddenly may make your condition worse.

If you need to have any type of surgery, you may need to temporarily stop using metoprolol. Be sure the surgeon knows ahead of time that you are using metoprolol.

Metoprolol is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

Hypertension often has no symptoms, so you may not even feel that you have high blood pressure. Continue using this medicine as directed, even if you feel well. You may need to use blood pressure medication for the rest of your life.

Warning

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Buy Acai Palm Seeds Here, Acai Palm

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Delivering the best quality since 2007, at AcaiPalmSeeds. com we are always growing with a global reach. Our customers range from home gardeners to agricultural producers with an interest in producing superfruits.

Our staff and network of growers are happy to answer any questions you may have about growing your own acai. Our customers have successfully grown their own acai in Australia, India, the United States and many places in between. We are dedicated to a high germination rate from our fresh seeds. We maintain ideal conditions to guarantee results.

Protecting People and Plants

Our Fresh Brazilian Seeds are inspected before leaving Brazil and by the USDA in New York City to not contribute to the spread of any unwanted pests. The process of cleaning, quarantine, and inspection makes sure we are only sending healthy seeds. If you have questions about shipping policies for your country, feel free to ask.

Know what is in your Acai

Many companies also blend acai with a various other fruits and keep the concentration a mystery. In a few growing seasons, you can be enjoying your own fresh, healthy juice from an acai palm tree in your own garden. While acai has become a very expensive commodity, we have given people around the world a chance to produce their own low cost anti-oxidant rich superberry. Many health drinks are priced so high it makes their health benefits not worth the cost. Growing your OWN acai means you will have a steady supply of fresh, low-cost, locally-grown superfruit. Fresh acai fruit is not seen outside of South America because the acai fruit breaks down in shipping. If you have a warm climate, you can enjoy fresh, pure, un-diluted berries from your acai trees.

Questions/Preguntas?

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Tangled Noodle Fragile History And The Art Of Pabalat, Pabalat

Candy wrapper art: Pabalat ng Pastillas de Leche

Not long ago, I read with great interest an article about Tukluhan . an obscure festival unique to the village of Santa Cruz in Marinduque Province, which takes place every May 15th on the feast day of San Isidro de Labrador (the Laborer), patron saint of farmers. The central event is a religious procession for which residents decorate fences, trees and other structures along the route with garlands of fruits, vegetables and various foodstuff. Parade-goers then eagerly collect¹ the hanging comestibles as they trail behind the passing procession, in what sounds like a rural Filipino hybrid of Mardi Gras, the Macy's Thanksgiving Day parade and a self-service Halloween.

As I read, I hoped the article would satisfy my need for details: When did this tradition start? Was it some cool pre-colonial pagan harvest ritual adapted to Catholic themes? Most importantly, why was it done in the first place? Unfortunately, I came across a paragraph that pained my history-loving heart: "Librada Ricamata, 75, who gathers and sells edible seashells for a living, said villagers can't remember when and how Tukluhan originated. 'By the time we were born, Tukluhan was already celebrated here,' said Ricamata. She said the festival has been held since the time of her parents. 'The tradition was passed from their generation to ours, and knowing its origin is not our concern anymore,' she said." from "Marinduque Villagers Reach Out for Tukluhan" (PDI 5/26/11) A Question of History

I couldn't disagree more with Ms. Ricamata's final statement - our histories should always be our concern. Why is knowing the origins of Tukluhan or any other tradition so vital? The answer is in the question. All other queries record factual details: Asking what defines the tradition and how tells us the manner in which it is done; who reveals the participants while when and where establish time and space. But why is a glimpse into elusive meaning - the answer shines a light, albeit dim or filtered, into the needs and motivation behind our customs, which in turn helps us to understand their importance to our personal and group identities. The answer to why allows us to look at ourselves from the perspective of the past.

Young folk musicians in Gasan, Marinduque, Easter '11

If the why is forgotten or brushed aside as irrelevant, then traditions may lose much of their powerful symbolism and risk becoming irrelevant themselves. How long might Tukluhan last if no one knows or seems to care why they participate in its festivities? Already, the custom is changing: according to the article, the foods displayed along the parade route traditionally came from the town's agricultural bounty. Now, they are slowly being replaced by packaged, processed items such as chips and candies. How has the festival's meaning been changed by this development? We can't know because without knowing its history, we have little reference to evaluate.

Celebrations and Crafts

In a kind of cultural Darwinism, unique traditions fall by the wayside all the time, unnoticed because they are so little known, much less practiced, beyond the communities in which they first developed. Happily, some find a measure of outside fame to ensure their continuation, like the Moriones Festival . which originated in a tiny Marinduque parish and is now world-famous. That such a local cultural event can remain vibrant may be due, I believe, to an important distinction that the Tukluhan lacks: an active interest in its history that remains central to its tradition.

The Moriones Festival is celebrated during Easter Holy Week in municipalities throughout the province and has inspired similar festivities all over the Philippines, but the townspeople of Mogpog proudly preserve the story of how their own Father Dionisio Santiago staged the first re-enactment over 200 years ago. Furthermore, even as their tradition becomes a tourist attraction, the residents who participate in it do so in faithful practice to the event's original intent as a time for penance and prayer.

Moriones parading through Mogpog, Marinduque/Easter '11

Such festive occasions stand a fair chance of survival, if only because everyone, including 'outsiders', has an opportunity to participate in some way, whether as players or spectators. More precarious, however, is the fate of small traditions such as time-consuming and skillful craftwork that have many admirers but dwindling numbers of practitioners. Without subsequent generations willing to learn about their histories or perpetuate the art, some craft traditions may suffer the sad indignity of being met with an indifferent shrug of the shoulders and set aside.

Paper-Cutting: Folk Art and Candy Wrappers

That is the possible future facing the Filipino folk art form called pabalat ². This lovely example of decorative paper-cutting is unique not only for being practiced primarily in one area, but also for its singular purpose - to make colorful wrappers for pastillas de leche . In a previous post. I discussed how the history of this Filipino milk candy is rather fuzzy for lack of recorded details; unfortunately, it extends to the special way this confection is presented. What little is known (or remembered) about how pabalat began is closely related to the origins of pastillas de leche in the town of San Miguel de Mayumo in Bulacan Province. But the reason behind why this particular candy, among all the many other treats and sweets, deserved such special wrappers has been lost.

Decorative paper-cutting is popular in the Philippines and its most recognized form is the famed parols . or Christmas lanterns, that sport fluttering 'comet tails' of delicately cut paper, of which pabalat is reminiscent. Filipino papercraft was likely adapted from Jian Zhi . the 1500-year old Chinese art of paper-cutting. Interestingly, jian zhi may have arrived in the Philippines via two routes - one direct, the other quite circuitous. Chinese traders and settlers probably brought paper-cutting directly to the islands, but a distinct influence may also have come from Mexico by way of the Manila-Acapulco galleon trade .

In pre-Hispanic Mesoamerica, Aztecs made a form of paper called amatl (Sp. amate ) from mashed tree bark, on which images of deities were cut out with stone knives. Spain's own history of papercraft³ began in the 12th century when the material and art were introduced by Muslim rulers and Arab traders who brought the practices back to the Middle East and Europe from Asia. After the Spanish conquest, the Aztec craft, influenced by its European colonizers, evolved into Mexico's distinctive papel picado ('perforated paper'), used to create festive banners for special occasions. The influence of Mexican papel picado on Filipino papercutting is strongest in the colorful flag garlands called banderitas (from Sp. bandera . 'flag'), which add festive decoration to local pistahans (festivals).

Papercut candy wrapper

Preserving the Past

Neither parols nor banderitas . however, are as closely related to a specific place and purpose as pabalat . Presumed to be as old as pastillas de leche . these pretty candy wrappers are made from papel de japon and were traditionally used as decorative table centerpieces in Bulacan's fine homes⁴. Sadly, this unique Bulakeno craft - once taught in local schools and practiced in many families - is slowly disappearing. Most practitioners are now elderly, their ranks dwindling, and pabalat is now often made only by special order in association with local pastillas - makers and retailers.

Concerned by the possibility of losing this folk tradition, master pabalat - maker Luz Ocampo⁵, affectionately known as Nanay (mom), still tirelessly practices and promotes her craft through media interviews and attendance at art shows and craft fairs, despite her nearly 90 years. Having learned the art at the age of twelve in her hometown of San Miguel (where pastillas de leche originated), Nanay Luz is determined to pass along as much of its history as she knows in hopes of keeping it alive for new generations.

Fascinated by the delicate beauty of pabalat and feeling a particular affinity because of my personal ties to Bulacan, ancestral home of my father's family, I was inspired to try my hand at it. I had never previously seen an actual pabalat . other than photographs on the web, but with some online guidance. I gave it a go. I hope that, in some small way, I can help preserve a small part of our history.

1. Tukluhan ostensibly means "to reach". However, I could not confirm to which Filipino dialect this word belongs, and my mother - born in Marinduque and a native Tagalog-speaker - is unfamiliar with it.

2. Pabalat comes from the Tagalog word balat . meaning a covering (e. g. skin, bark, peel, husk, etc.)

3. Although Spain does not have a specific, named tradition of paper-cutting (at least, none that I could find online), the introduction of paper and papercraft to the region by Muslim traders was apparently the originating point for vibrant paper-cutting arts in other European cultures. The oldest may be the Jewish form. which is traditionally used to decorate mizrachs (a wall plaque indicating direction of prayer) and ketubahs (marriage contracts). Other papercut art forms include Scherenschnitte ('scissor cuts') in Germany and the Polish wycinanki .

Pabalat ng Pastillas de Leche

No recipe today! Instead, check out my earlier post about Pastillas de Leche for a recipe, then try crafting some pabalat for the candies you make or, as a quick alternative, use store-bought pastillas and other small candies such as Tootsie Rolls.

Materials and Tools

Papel de japon (tissue paper) in different colors Ruler Pencil Fine-tipped scissors (curved cuticle scissors work beautifully!)

To make 2 wrappers:

Cut 1 sheet of tissue paper to 13.5 inches long by 10 inches wide. Fold in half lengthwise, then fold in half again lengthwise. The folded sheet should now be 13.5" long by 2.5" wide. Using a ruler, mark off a 4" x 2.5" section: this will be portion where the pastillas/candy will be wrapped and should remain uncut.

With a pencil, draw your pattern! A workable design is part trial, part error and all personal creativity. Start by drawing simple shapes such as flowers or stars all over the area. Then, 'connect' the shapes together by drawing 'bands' between them. For best results, keep the cut-out sections small but numerous to get a more lacy look. I also suggest keeping the edges intact to give the pabalat more structure and support.

With fine-tipped/cuticle scissors, begin cutting, starting inside and working out toward the edges. Don't worry about perfectly following your pencil lines - they will show up only on one panel. Besides, I think it adds a quaint roughness, a hand-made quality to the pabalat .

When done, open the sheet and cut in half lengthwise to make 2 panels. Take one half-sheet and cut in half again, beginning at the top of the cut-out section and stopping just at the untouched 4" x 2.5" portion.

If using homemade pastillas . wrap each piece in wax paper or plastic wrap to keep any moisture from saturating the paper. Place the candy lengthwise on the uncut portion of the pabalat and roll up, then gently twist both ends to close.

Place the pabalat - wrapped pastillas in a bowl or glass jar to show off your handiwork!

Elizabeth - Yes! I read how pabalat & fruit carving go almost hand-in-hand in Bulacan as food folk art. But it would take a lot of skill for the carving - I'll stick to paper cutting for now. Definitely, we will have to plan something when come here! 8-)

Malou - Thank you! I never knew about pabalat either until I was doing research into pastillas. It would be a terrible shame if this folk art died out or became completely mechanized. I love doing crafty stuff so it was fun to try my hand at pabalat making. I'm thinking they might make good gifts. 8-)

Lisa - When I saw photos of Nanay Luz's pabalat, I fell in love with all the colorful paper. As far as I've read, almost all of the cutting is done with scissors, although one article did mention that NL's tools did include a small blade. I stuck with a $1 pair of cuticle scissors. 8-)

Elin - Thank you so much! It was my pleasure to share as I truly enjoyed making them. It was indeed slow going (my first one took close to an hour!) but it's got much easier. 8-)

Chef_d - I'm so happy you enjoyed it! I honestly don't recall ever seeing pabalat before, or maybe, just as you noted, I didn't pay attention as a child. Intricate designs such as Nanay Luz's take a lot of skill and talent, but this form of paper cutting isn't really that hard - I hope others will take it up! 8-)

Ate - Martha has nothing to worry about but thank you! I will have to make some special ones for you on your next visit! 8-)

Joy - Thank you! There's something rather soothing about cutting - a good time to meditate. I'm hoping to make them (along with homemade pastillas) as gifts for family and friends this upcoming holiday season! 8-)

Kat - Aren't they lovely? I can only imagine how tables with dozens and dozens of these wrapped candies must look like! 8-)

Sophia - As you noted on your own post about artist and journalist personalities, I share your curiosity about the stories behind people, art, events, etc. We can't forget what and who came before us! As for talent, you are way too kind - I do love being crafty, though! 8-)

Forager - Yay! I hoped that the photos would do justice to the these wrappers. I left out some colors but can't wait to add to the rainbow! 8-)

Those are incredible. Quite the marketing piece for your blog. ) With being in the middle of summer around here there are plenty of festivals going on. However, they just don't spark my interest like the ones abroad. We have some history going on, but it's nothing like the history and traditions of what I've experienced in other countries. Such an interesting summary here.

I always learn something interesting and new when I come visit your blog! I was really struck by the comments early in your post about Tukluhan and people not really knowing it's origins. It saddens me to think of a people not knowing their own history like that. I am fascinated by local history where I am as it relates directly to my ancestry, while I understand this interest may be a luxury for some it seems it should also be a necessity. Those who do not understand their own history are doomed to repeat it. ok so that isn't a direct quote but you get the gist. I think that the loss of history on any scale is a cultural loss for us all. On the other hand I adore your papercuts and the detail, they are beautiful!

Macrogol Oral Powder Compound, Lyopraz

MACROGOL ORAL POWDER COMPOUND

Transcript

PACKAGE LEAFLET: INFORMATION FOR THE USER

If any of these apply to you, please talk to your doctor or pharmacist for further advice.

Macrogol Oral Powder, Compound

Take special care with Macrogol Oral Powder, Compound

Powder for oral solution Read all of this leaflet carefully because it contains important information for you. This medicine is available without prescription. However, you still need to take Macrogol Oral Powder, Compound carefully to get the best results from it. • Keep this leaflet. You may need to read it again. • Ask your pharmacist if you need more information or advice. • You must contact a doctor if your symptoms worsen or do not improve after 14 days for chronic constipation, or after 3 days for faecal impaction. • If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or your pharmacist. In this leaflet: 1. What Macrogol Oral Powder, Compound is and what it is used for 2. Before you take Macrogol Oral Powder, Compound 3. How to take Macrogol Oral Powder, Compound 4. Possible side effects 5. How to store Macrogol Oral Powder, Compound 6. Further Information

1. What Macrogol Oral Powder, Compound is and what it is used for The name of this medicine is Macrogol Oral Powder, Compound It is a laxative for the treatment of chronic constipation in adults, children (aged 12 years and above) and the elderly. •

It helps you to have a comfortable bowel movement even if you have been constipated for a long time. It also works in very bad constipation called faecal impaction (complete severe constipation).

2. Before you take Macrogol Oral Powder, Compound Do not take Macrogol Oral Powder, Compound if you are allergic (hypersensitive) to macrogol 3350, sodium chloride, sodium hydrogen carbonate, potassium chloride or any of the other ingredients listed in section 6. • if you have a perforated gut wall. • if you have a blockage in your intestine (gut obstruction, ileus) for example by paralysis of the intestine. • if you have severe inflammatory bowel disease like ulcerative colitis, Crohn’s disease or toxic megacolon.

If you develop side effects such as swelling, shortness of breath, feeling tired, dehydration (symptoms include increasing thirst, dry mouth and weakness) or heart problems you should stop taking Macrogol Oral Powder, Compound and contact your doctor immediately. Do not take Macrogol Oral Powder, Compound for longer periods of time unless you have been instructed to do so by your doctor; for example if you take drugs that can cause constipation or if you have a disease which causes constipation for example Parkinson’s disease or multiple sclerosis (MS). Taking other medicines Please inform your doctor or pharmacist if you are taking, or have recently taken, any other medicines, including medicines obtained without a prescription. Pregnancy and breast-feeding There is no documented experience from the use of macrogol in pregnant women or during breast-feeding. However no effects during pregnancy or on the breastfed newborn/infant are anticipated, since systemic exposure to macrogol is negligible. Therefore Macrogol Oral Powder, Compound can be used during pregnancy or while breast-feeding if necessary. Ask your doctor or pharmacist for advice before taking any medicine. Driving and using machines Macrogol Oral Powder, Compound has no effect on the ability to drive or use machines.

3. How to take Macrogol Oral Powder, Compound Always take Macrogol Oral Powder, Compound exactly as your doctor or pharmacist has told you. You should check with your doctor or pharmacist if you are not sure. This medicine can be taken at any time with or without food or drink. Chronic Constipation (constipation for a long time) Dosage - adults and children above 12 years 1 sachet one to three times daily. The normal dose for most patients is 1-2 sachets per day. Depending on the individual response 3 sachets per day might be needed. The dose depends on the severity of your constipation. The dose can be adjusted down to the lowest effective dose after a couple of days. The time of the treatment is normally 2 weeks. If the symptoms persist after 2 weeks of treatment contact your doctor. Children (below 12 years of age) Not recommended. Patients with renal insufficiency No dosage change is necessary for treatment of chronic constipation.

Other side effects include: headaches, high and low levels of potassium in the blood.

Patients with a heart condition Do not take more than 2 sachets in one hour.

Faecal Impaction (complete severe constipation) Before you take this medicine for faecal impaction, it should be confirmed that you have this condition.

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Dosage – adults and children above 12 years The usual dose for faecal impaction (complete severe constipation) is 8 sachets daily. The 8 sachets should be taken within a 6 hour period each day for up to 3 days if required.

5. How to store Macrogol Oral Powder, Compound

Patients with renal insufficiency No dosage change is necessary for treatment of faecal impaction. Patients with a heart condition Do not take more than 2 sachets in one hour. Method of Administration Dissolve the contents of 1 sachet in a glass of water (125ml or ? pint), stir well and drink. If you are being treated for faecal impaction it may be easier to dissolve all 8 sachets in 1 litre of water. If you take more Macrogol Oral Powder, Compound than you should You may develop diarrhoea. Stop taking Macrogol Oral Powder, Compound until it clears, then start again at a lower dose. If you are worried contact your doctor or pharmacist. If you forget to take Macrogol Oral Powder, Compound Take the dose as soon as you remember and then continue on as before. Do not take a double dose to make up for a forgotten dose.

4. Possible side effects Like all medicines, Macrogol Oral Powder, Compound can cause side effects, although not everybody gets them. If you experience any of the following side effects, stop taking Macrogol Oral Powder, Compound and see your doctor immediately: • a serious allergic reaction which causes difficulty in breathing or dizziness, or swelling of the face, lips, tongue or throat. • signs of an allergy, such as a rash, itching or shortness of breath. The following side effects have also been reported: • Common (occur in more than 1 in 100 users): stomach rumbling, swollen stomach or stomach pain, suffering from wind, vomiting, feeling sick, indigestion or a sore anus (bottom). If you experience mild diarrhoea when you start to take Macrogol Oral Powder, Compound your condition will generally get better if you reduce the amount of Macrogol Oral Powder, Compound you take. • Very rare (occur in less than 1 in 10,000 users): hives, reddening of the skin or a nettle rash, swelling of the hands, feet or ankles.

Unopened sachet: No special storage conditions. Once you have made up Macrogol Oral Powder, Compound in water, if you cannot drink it straight away keep it covered and store in a refrigerator (2°C – 8°C). Throw away any solution not used within a 24 hour period. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

6. Further Information What Macrogol Oral Powder, Compound sachets contain The active substances are macrogol 3350 (13.125g), sodium chloride (350.7mg), sodium hydrogen carbonate (178.5mg) and potassium chloride (46.6mg). The other ingredients are lemon flavour and acesulfame potassium (E950) as a sweetener. The lemon flavour contains the following ingredients: acacia gum (E414) and flavouring. What Macrogol Oral Powder, Compound looks like and contents of the pack Macrogol Oral Powder, Compound is a white powder packed in sachets. It is available in boxes of 8, 10, 20, 30, 50 or 100 sachets. Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer: Chanelle Medical Loughrea, Co Galway, Ireland Distributor: Co-pharma Limited Unit 4, Metro Centre, Tolpits Lane, Watford, Hertfordshire, WD18 9SS, UK This leaflet was last approved in 02/2015

Children (below 12 years of age) Not recommended.

Keep out of the reach and sight of children. Do not use Macrogol Oral Powder, Compound after the expiry date which is stated on the carton and sachet. The expiry date refers to the last day of that month.

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Emizof, Emizof

Zofran is used for preventing nausea and vomiting associated with cancer chemotherapy or surgery. Zofran is a serotonin 5-HT 3 receptor blocker. It works by blocking a chemical thought to be a cause of nausea and vomiting in certain situations (eg, chemotherapy).

Use Zofran as directed by your doctor.

Take Zofran with a full glass of water.

This medicine can be taken with or without food.

Do not take the medication in larger amounts, or take it for longer than recommended by your doctor.

If you miss a dose of Zofran, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Zofran.

Store Zofran at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zofran out of the reach of children and away from pets.

Active Ingredient: Ondansetron.

Do NOT use Zofran if:

you are allergic to any ingredient in Zofran

you are taking apomorphine.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Zofran. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have had an allergic reaction to another serotonin 5-HT 3 receptor blocker (eg, dolasetron, granisetron)

if you have liver problems or a certain type of irregular heartbeat (QT prolongation, long QT syndrome).

Some medicines may interact with Zofran. Tell your health care provider if you are taking any other medicines, especially any of the following:

Apomorphine because the risk of its side effects may be increased by Zofran

Antineoplastic agents (eg, cyclophosphamide) because their effectiveness may be decreased by Zofran.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Zofran 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.

Important safety information:

Zofran may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Zofran with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Zofran should be used with extreme caution in children younger 4 months; safety and effectiveness in these children have not been confirmed. Certain strengths of Zofran are not recommended in children. If you have questions about using Zofran in children, contact your doctor or pharmacist.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zofran while you are pregnant. It is not known if Zofran is found in breast milk. If you are or will be breast-feeding while you use Zofran, check with your doctor. Discuss any possible risks to your baby.

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:

Constipation; diarrhea; dizziness; drowsiness; headache; tiredness.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue; wheezing; unusual hoarseness); chest or jaw pain; fainting; fast, slow, or irregular heartbeat; fever; numbness of an arm or leg, or sudden severe headache or vomiting; seizures; severe or persistent dizziness; skin tingling or numbness; stomach pain; trouble urinating; uncontrolled muscle movements; vision changes or loss.

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.

Comprar Dartelin (Trental) Sin Receta, Dartelin

compra Dartelin (Trental) en linea sin receta

Dartelin (Trental) Explicacion

Dartelin se utiliza en lo que respecta a hacer frente a la claudicacion irregular (dolor, dolores de calambres, hormigueo, o incluso un poco de debilidad en los pies, con estilo, muslo, nalgas) o incluso en algunos enfermos. Esto tambien puede suministrar para algunas otras circunstancias.

Dartelin es realmente un tipo xantina circulacion de la sangre de refuerzo. Funciones a traves de la perdida de sangre, asi como la mejora de la versatilidad celular de color rojo sangre, que evoca el torrente sanguineo con el fin de la circulacion mucho mas abiertamente con los vasos sanguineos.

Dartelin tambien puede ser referido como Dartelin.

titulo general asociada con Dartelin Dartelin es en realidad.

Marca asociada con Dartelin Dartelin es en realidad.

Dartelin (Trental) Dosis

Dartelin viene en:

400mg material de friccion dosis regular

Obtener Dartelin por via oral junto con las comidas o incluso productos lacteos.

Consumir entero. Por lo general, no se agrietan, moler, o incluso masticar antes de ingerir.

Si usted desea lograr mejores resultados por lo general no dejar de usar Dartelin de repente.

Dartelin (Trental) Careciendo asocia con dosis

Por lo general, no reciben doble dosis. En caso de que salte la dosis que necesita para llevar una vez se tiene en cuenta en lo que respecta a su deficiente. Cuando es hora de la dosis que necesita para llevar a cabo su propia rutina de dosificacion normal.

Dartelin (Trental)

En el caso de una sobredosis Dartelin y que tambien se evita gran usted necesita comprobar hacia fuera su medico o incluso el medico de inmediato.

Dartelin (Trental) Espacio de almacenamiento

Tienda en temperaturas de espacio entre 10 y 30 niveles de D (59, asi como ochenta y seis niveles F) de la humedad, la iluminacion, asi como la temperatura. Mantener cuadro de texto firmemente cerrada. Fortalecer cualquier tipo de medicamento sin tocar a partir del dia de vencimiento. Mantener desde el lograr de los ninos dentro de un cuadro de texto que los ninos pequenos no puedan abrir.

Dartelin (Trental) Efectos negativos

Dartelin ofrece los efectos negativos. El mas tipico tienden a ser:

eructos material de friccion

material de friccion hinchazon

material de friccion vision borrosa

diarrea friccion materiales

material de friccion fatiga

lavado material de friccion

material de friccion de combustible

material de friccion dolor de cabeza

acido material de friccion de reflujo

nauseas o vomitos material de friccion

material de dolor de panza friccion

Mucho menos tipicos y graves efectos negativos en todo el uso de Dartelin:

respuestas reaccion alergica (urticaria, inhalando y exhalando, cuestiones de alergia, asi como la erupcion) material de friccion

material de friccion problemas del corazon

cardiaco anormal vencio friccion materiales

vomitando material de friccion

Los efectos negativos son indicaciones se basan en medicamentos que podrian estar utilizando pero, ademas, se basan en su condicion de bienestar y otros aspectos.

Dartelin (Trental) Contraindicaciones

Por lo general no reciben Dartelin en caso de que son sensibles con el fin de Dartelin elementos o metilxantinas (teofilina, cafe, teobromina).

Hacerse cauteloso junto con Dartelin en caso de que usted esta esperando, van a quedar embarazada. Dartelin se puede encontrar en los senos lacteos. Por lo general no amamantar a sus hijos durante el uso de Dartelin.

Por lo general no reciben Dartelin para aquellos que han experimentado la perdida de sangre actual dentro de la mente o incluso los ojos.

Informe a su medico o profesional de la odontologia que se obtiene Dartelin antes de recibir cualquier tipo de atencion medica o incluso la higiene dental, tratamiento de emergencia inesperada, o incluso tratamiento quirurgico.

El proceso puede durar de dos a fin de cuatro semanas para ver la mejora en su problema, o mas de ocho semanas con respecto a la mitigacion de la optima.

Utilice Dartelin junto con precaucion extrema en las personas mayores. Pueden ser mucho mas delicado con el fin de los resultados.

Evite las bebidas alcoholicas.

Prevenir itinerante dispositivo.

Puede ser danino para evitar el uso de Dartelin de repente.

Dartelin (Trental) Preguntas comunes

Queen: ?Que es exactamente Dartelin?

El: Dartelin se utiliza en lo que respecta a hacer frente a la claudicacion irregular (dolor, dolores de calambres, hormigueo, o incluso un poco de debilidad en los pies, con estilo, muslo, nalgas) o incluso en algunos enfermos. Esto tambien se puede suministrar por alguna otra circumstances. A

Queen: Entonces, ?como funciona exactamente la funcion Dartelin?

El: Dartelin es realmente un tipo xantina circulacion de la sangre de refuerzo. Funciones a traves de la perdida de sangre, asi como la mejora de color rojo versatilidad celular torrente sanguineo, que evoca el torrente sanguineo con el fin de la circulacion mucho mas abiertamente con la sangre vessels. A

Queen: Muy mejor titulo general?

El: titulo general asociada con Dartelin es en realidad Dartelin. A

Queen: Exactamente ?que debo FAG situacion asociada con careciendo dosis?

El: En el caso de la dosis carente de lo necesario para el fin de la pildora tan pronto como sea posible. Por lo general, no reciben doble dosis. Y cuando lo que realmente es el tiempo mas afortunado para la dosis que necesita para llevar a cabo su propia rutina normal asociada con Dartelin using. A

Queen: Exactamente ?Que debo evitar mientras uso Dartelin?

El: Si bien el uso de Dartelin a prevenir el consumo de alcohol, dispositivo traveling. A

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Busqueda

Las Personas Tambien Buscan

Mefenan Rezeptfrei Kaufen ? Qualitat; ? Mit Niedrigen Preisen; ? Lieferung, Mefenan

Ponstel (Mefenamic Acid) ist in einer Gruppe von Medikamenten, den sogenannten nichtsteroidalen Antirheumatika (NSAIDs). Mefenaminsaure wirkt, indem es Hormone, die Entzundungen und Schmerzen im Korper verursachen.

Mefenaminsaure wird verwendet, um Schmerzen oder Entzundungen von Arthritis. Es wird auch verwendet, um Menstruationsbeschwerden behandeln.

Mefenaminsaure kann auch fur andere Zwecke, die nicht in dieser Anleitung Medikamente verwendet werden.

Nehmen Sie dieses Medikament genau wie es Ihnen verschrieben wurde. Nehmen Sie nicht die Medikamente in gro?eren Mengen, oder nehmen Sie langer als empfohlen von Ihrem Arzt. Befolgen Sie die Anweisungen auf dem Etikett Verschreibung.

Wenn Sie Mefenaminsaure fur eine lange Zeit in Anspruch nehmen, kann Ihr Arzt mochte Sie auf einer regelma?igen Basis, um sicherzustellen, dieses Medikament ist nicht die schadliche Wirkungen verursacht uberprufen. Verpassen Sie nicht die geplanten Besuche bei Ihrem Arzt.

Nehmen Sie das Medikament wie von Ihrem Arzt verordnet wurde.

Suchen Sie Notfall medizinische Aufmerksamkeit, wenn Sie denken, Sie haben zu viel von dieser Medizin verwendet. Uberdosierung Symptome konnen Ubelkeit, Erbrechen, Bauchschmerzen, Schwindel, Schlafrigkeit, schwarzer oder blutiger Stuhl, Bluthusten, Wasserlassen weniger als ublich oder uberhaupt nicht, flache Atmung, Ohnmacht oder Koma.

Bewahren Mefenaminsaure bei Raumtemperatur weg von Feuchtigkeit, Hitze und Licht.

Dieses Medikament kann das Risiko erhohen, lebensbedrohliche Herz-oder Kreislaufproblemen, einschlie?lich Herzinfarkt oder Schlaganfall. Verwenden Sie nicht dieses Medikament kurz vor oder nachdem Herz-Bypass-Operation (auch als koronare Bypass-Operation oder CABG).

Suchen Sie Notfall medizinische Hilfe, wenn Sie Symptome von Herz-Kreislauf-Probleme, wie Schmerzen in der Brust, Schwache, Kurzatmigkeit, undeutliches Sprechen, oder Probleme mit der Vision oder dem Gleichgewicht haben.

Dieses Medikament kann auch Ihr Risiko fur schwerwiegende Auswirkungen auf den Magen oder Darm, einschlie?lich Blutung oder Perforation (Bilden eines Lochs). Diese Bedingungen konnen todlich sein und gastrointestinale Effekte konnen ohne Vorwarnung jederzeit auftreten, wahrend Sie Mefenaminsaure werden. Altere Erwachsene konnen ein noch gro?eres Risiko fur diese schweren gastrointestinalen Nebenwirkungen.

Rufen Sie Ihren Arzt sofort, wenn Sie Symptome von Blutungen in Magen oder Darm haben. Dazu gehoren schwarz, blutig, oder Teerstuhle, oder Bluthusten oder Erbrochenes, dass wie Kaffeesatz aussieht.

Verwenden Sie keine anderen over-the-counter kalt, Allergie, oder Schmerzmittel, ohne vorher zu fragen Sie Ihren Arzt oder Apotheker.

Trinken Sie keinen Alkohol wahrend der Einnahme von Mefenaminsaure. Alkohol kann das Risiko von Magen Blutungen.

Informieren Sie Ihren Arzt, wenn Sie ein Antidepressivum sind wie Citalopram (Celexa), Duloxetin (Cymbalta), Escitalopram (Lexapro), Fluoxetin (Prozac, Sarafem, Symbyax), Fluvoxamin (Luvox), Paroxetin (Paxil), Sertralin (Zoloft), oder Venlafaxin (Effexor). Einnahme dieser Medikamente mit Mefenaminsaure konnen Sie Quetschung zu bekommen oder leicht zu verbluten.

Bevor Mefenaminsaure, informieren Sie Ihren Arzt, wenn Sie eines der folgenden Medikamente:

Blutverdunner wie Warfarin (Coumadin);

einem Diuretikum (Wasser-Pille) wie Furosemid (Lasix);

Cyclosporin (Gengraf, Neoral, Sandimmun);

Lithium (Eskalith, Lithobid);

Methotrexat (Rheumatrex, Trexall);

Steroide (Prednison und andere); oder

Aspirin oder NSAR (nicht-steroidale Antirheumatika) wie Diclofenac (Voltaren), Etodolac (Lodine), Fenoprofen (Nalfon), Flurbiprofen (Ansaid), Ibuprofen (Advil, Motrin), Indomethacin (Indocin), Ketoprofen (Orudis). Ketorolac (Toradol), Meclofenamat (Meclomen), Meloxicam (Mobic), Nabumeton (Relafen), Naproxen (Aleve, Naprosyn), Piroxicam (Feldene), und andere.

Diese Liste ist nicht vollstandig und kann es auch andere Medikamente, die mit Mefenaminsaure interagieren konnen. Informieren Sie Ihren Arzt uber alle verschreibungspflichtigen und OTC-the-counter Medikamente, die Sie verwenden. Dazu gehoren Vitamine, Mineralien, pflanzliche Produkte, Medikamente und durch andere Arzte. Beginnen Sie nicht mit einem neuen Medikament ohne Rucksprache mit Ihrem Arzt.

Hifalutin - Definition Of Hifalutin By The Free Dictionary, Flutin

hifalutin

References in periodicals archive ?

Dodgy Dave's oration coincided with a histrionic defence of private education by Richard Harman, chairman of the Headmasters' and Headmistresses' Conference (no, I'd never heard of him or his hifalutin outfit either).

While all that may sound hifalutin. in the same way, building her own house has given Anson a similar and much deeper appreciation of the intricacies involved in creating a place to live.

In these times of recession, street food feels very affordable and it makes sense of all those hifalutin concepts that food magazines are bandying around these days - it's 'local' and 'seasonal' just because traders tend to grab whatever is cheapest at the market.

Save hifalutin vocabulary for other lawyers, if you must, and speak to the jurors in plain English, she recommends.

hifalutin

References in periodicals archive ?

Dodgy Dave's oration coincided with a histrionic defence of private education by Richard Harman, chairman of the Headmasters' and Headmistresses' Conference (no, I'd never heard of him or his hifalutin outfit either).

While all that may sound hifalutin. in the same way, building her own house has given Anson a similar and much deeper appreciation of the intricacies involved in creating a place to live.

In these times of recession, street food feels very affordable and it makes sense of all those hifalutin concepts that food magazines are bandying around these days - it's 'local' and 'seasonal' just because traders tend to grab whatever is cheapest at the market.

Save hifalutin vocabulary for other lawyers, if you must, and speak to the jurors in plain English, she recommends.

Kopen Advil-Mono (Motrin) Zonder Recept, Advil-Mono

Advil-mono (Motrin) Kopen Online Zonder Recept

Advil-mono (Motrin) Toelichting

Advil-mono is eigenlijk gemaakt samen met geschikte drug-store methode creeren Advil-mono fantastische tool richting ongemak, temperatuur, zwelling. Focus op geassocieerd met Advil-mono zou zijn om ongemak te voorkomen.

Advil-mono kan zo bekend medicatie die niet alleen kon bieden bescherming tegen onaangename gevoel, maar bovendien deze waarborgen door middel van temperatuur passeren. Advil-mono werkt belemmerende lichamelijke hormonen geassocieerd met ongemak.

Advil-mono kan ook worden aangeduid als Ibuprofen, Brufen, Ibugesic, Advil, Anadin Ibuprofen, Arthrofen, Cuprofen, Fenbid, Galprofen, Hedex Ibuprofen, Ibufem, Librofem, Mandafen, Manorfen, Migrafen, Nurofen, Obifen, Relcofen.

Advil-mono eigenlijk NSAIDs (niet-steroide anti-inflammatoire geneesmiddelen).

Ibuprofen kan niet worden gebruikt door patienten onder een.

General titel geassocieerd met Advil-mono is eigenlijk Ibuprofen.

Merken geassocieerd met Advil-mono neiging om Advil-mono, Genpril, IBU, Ibu-Tab, Midol IB, Menadol, Focused Falls, Captabs, Haltran, Midol, Nuprin, Advil, Rufen, Pediacare temperatuur zijn.

Advil-mono (Motrin) Dosis

Advil-mono komt in:

200mg lagere dosis frictiemateriaal

400mg normale dosis frictiemateriaal

600mg Verbeterde Dose frictiemateriaal

Advil-mono kan worden geconsumeerd in soort pillen (200 miligrams, vierhonderd miligrams, zeshonderd mg), vloeistof tabletten, kauwtabletten, valt die zouden moeten oraal worden gebruikt.

Het is raadzaam om Advil-mono elke dag overwegen zonder diner en zuivel.

Krijg Advil-mono onthoud die de dosis is afhankelijk van iemands welzijn conditie.

De normale maximale Advil-mono dosis is eigenlijk achthonderd miligrams als een 1 dosering of zelfs 3200 miligrams elke dag (maximaal 4 doses).

Ibuprofen kan niet worden gebruikt door patienten onder een.

Wilt u beste resultaten te bereiken meestal niet stoppen met het gebruik van Nurofen ineens.

Advil-mono (Motrin) ontbreekt in verband met de dosering

Meestal krijgt niet de dubbele dosering. In het geval u de dosering die u nodig hebt om het te dragen als je eenmaal in het achterhoofd te houden met betrekking tot uw ontbreekt overslaan. Wanneer het tijd is voor de dosering die u nodig hebt om te dragen op je eigen normale dosering routine.

Advil-mono (Motrin) Overdose

In het geval u Advil-mono overdosis en je ook voorkomen dat geweldig je nodig hebt om direct te controleren uw arts of zelfs arts. Geassocieerd met Advil-mono overdosering: out of control ogen acties, gloeiende blauwe kleur over lippen, mond gebied, evenals neus-gebied, langzamer en uitademen, gevoel licht in het hoofd.

Advil-mono (Motrin) Opslagruimte

Shop in de ruimte een temperatuur tussen 10 en 30 niveaus D (59 en zesentachtig niveaus F) tegen vocht en temperatuur. Handhaaf tekstvak stevig dicht. Versterken elke vorm van ongerepte medicatie na het verstrijken dag. Handhaven van het bereiken van kinderen.

Advil-mono (Motrin) Negatieve effecten

Advil-mono biedt de negatieve effecten. De meest typische neiging om:

migraine frictiemateriaal

bloatedness frictiemateriaal

matig zure reflux frictiemateriaal

rinkelen in de oren frictiemateriaal

diarree frictiemateriaal

gevoel ijlend frictiemateriaal

brandstof frictiemateriaal

congestie frictiemateriaal

frustratie frictiemateriaal

wazig gezichtsvermogen frictiemateriaal

vermoeidheid frictiemateriaal

Veel minder typische en ernstige nadelige gevolgen voor de hele behulp Advil-mono :

allergische reactie reacties (urticaria, en uitademen problemen, allergie, evenals eruptie) frictiemateriaal

stabiliteitsproblemen frictiemateriaal

geelzucht frictiemateriaal

ongemak in verband met weer terug frictiemateriaal

De montering frictiemateriaal

verdoving frictiemateriaal

lagere temperatuur frictiemateriaal

onvoldoende vermogen frictiemateriaal

hinderlijk plassen frictiemateriaal

onduidelijke talk frictiemateriaal

hobbels frictiemateriaal

ongemak in verband met bovenlichaam frictiemateriaal

snelle hartslag frictiemateriaal

heesche frictiemateriaal

misselijkheid of braken frictiemateriaal

spierweefsel enige zwakte wrijving materiaal

onvoldoende honger frictiemateriaal

klei-gekleurde barkrukken frictiemateriaal

zetten op gewicht frictiemateriaal

zwakkeling, donker of zelfs teerachtige barkrukken frictiemateriaal

lichte huid frictiemateriaal

hinderlijk inname frictiemateriaal

dyspnoe frictiemateriaal

enige zwakte frictiemateriaal

Negatieve effecten zijn er aanwijzingen afhankelijk zijn van medicijnen die u zou kunnen gebruiken, maar bovendien rekenen op uw welzijn conditie en andere aspecten.

Advil-mono (Motrin) Contra-indicaties

Meestal niet Advil-mono te krijgen in het geval u gevoelig om Advil-mono elementen of aspirine zijn.

Speel de rol van voorzichtig wanneer gebruiken Advil-mono wanneer u verwacht en hebben nurseling.

Ibuprofen kan niet worden gebruikt door patienten onder een.

Meestal niet gebruiken Advil-mono voorafgaand aan of direct na CABG (hart vermijden chirurgie).

speelt de rol van voorzichtig met Ibuprofen bij gebruik van dit soort geneesmiddelen omdat glyburide (Micronase, DiaBeta); cyclosporine (Gengraf, Neoral, Sandimmune); steroide medicijnen (prednison); aspirine of zelfs sommige andere NSAID omdat naproxen (Aleve, Naprosyn), ibuprofen (Advil, Advil-mono), ketoprofen (Orudis), indomethacine (Indocin), diclofenac (Voltaren), etodolac (Lodine); ADVISEUR inhibitor omdat ramipril (Altace), moexipril (Univasc), perindopril (Aceon), enalapril (Vasotec), fosinopril (Monopril), benazepril (Lotensin), quinapril (Accupril), captopril (Capoten), trandolapril (Mavik), lisinopril ( Zestril, Prinivil); methotrexaat (Rheumatrex, Trexall); diuretica omdat furosemide (Lasix); lithium (Eskalith, Lithobid); bloedbaan slanker omdat warfarine (Coumadin).

Speel de rol van voorzichtige, samen met Advil-mono in het geval van het krijgen van hypertensie, nier-, hart - of zelfs ziekten in de lever, ademhalingsmoeilijkheden, congestief hart - falen, bloedbaan klomp, buik zweren, hartaanval, neus-gebied poliepen, darmproblemen, bloedverlies, diverticulose.

Voorkom alcoholische dranken.

Gebruik Advil-mono nauwgezet in het geval u wenst te gaan door middel van een chirurgische ingreep (tandheelkundige of een soort van andere).

speelt de rol van voorzichtig met Ibuprofen bij krijgen fenylketonurie.

Blijf weg van aspirine gebruik.

Advil-mono kon niet echt zekerheid met betrekking tot de senioren.

Speel de rol van voorzichtige, samen met zonnestralen. Advil-mono kunnen porien en de huid delicaat om de zon te maken. Safeguard porien en de huid door de zon.

Het kan schadelijk zijn voor Advil-mono te voorkomen met behulp van ineens.

Advil-mono (Motrin) Veelgestelde vragen

Queen: Precies wat doet Advil-mono impliceren?

De: Advil-mono is echt een ster-kwaliteit geneeskunde in strijd richting ongemak en zwelling die wordt veroorzaakt door gewrichtsaandoeningen (artrose, artritis reumatoide, gouty gewrichtsaandoeningen, psoriatische gezamenlijke ziekte, ziekte van Bechterew), migraine, rugpijn, spiermassa pijnen, kiespijn, kleine verwondingen. Nurofen is een goed idee met betrekking tot patienten, samen met temperature. A

Queen: Wat zijn precies algemene evenals merken geassocieerd met Advil-mono?

De: General titel geassocieerd met Advil-mono is eigenlijk Ibuprofen. Merken geassocieerd met Advil-mono neiging om Advil-mono, Genpril, IBU, Ibu-Tab, Midol IB, Menadol, Focused Falls, Captabs, Haltran, Midol, Nuprin, Advil, Rufen, Pediacare Temperature. A zijn

Queen: Wat er precies wordt voorgesteld te worden voorkomen?

De: Wilt u het beste resultaat te bereiken, zonder negatieve effecten is het raadzaam om alcoholische dranken te voorkomen. De rol van voorzichtig met Ibuprofen bij krijgen fenylketonurie. Meestal niet gebruiken Advil-mono voorafgaand aan of direct na CABG (hart vermijden chirurgie). Maak gebruik van Advil-mono minutieus in het geval u wenst te gaan door middel van een chirurgische ingreep (tandheelkundige of een soort van andere). Voor Advil-mono het is echt schadelijk om te roken. Blijf weg van aspirine gebruik. Speel de rol van voorzichtige, samen met zonnestralen. Advil-mono kunnen porien en de huid delicaat om de zon te maken. Safeguard porien en de huid door de sunlight. A

Queen: Hoe kan echt Advil-mono lopen?

De: Advil-mono kan zo bekend medicatie die niet alleen kon bieden bescherming tegen onaangename gevoel, maar bovendien dit te waarborgen door temperatuur passeren. Advil-mono werkt belemmerende lichamelijke hormonen geassocieerd met ongemak en airconditioning hele body. A

Queen: echt Advil-mono bezitten leeftijdsgroep te beperken?

De: Ibuprofen kan niet worden gebruikt door patienten onder A. A

Kopen Advil-mono (Motrin) online, kopen Advil-mono (Motrin) online zonder voorschrift, kopen Advil-mono (Motrin) zonder recept, kopen Advil-mono (Motrin) goedkoop, kopen Advil-mono (Motrin) zonder voorschrift, kopen Advil-mono (Motrin) uit Canada, kopen Advil-mono (Motrin) Canada, inkopen Advil-mono (Motrin) online, inkopen Advil-mono (Motrin) online no prescription, bestelling Advil-mono (Motrin) zonder recept, Advil-mono (Motrin) orale pil

Zoeken

Macrobid Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Macrobid

Macrobid

Uses

This medication is an antibiotic used to treat bladder infections (acute cystitis). It works by stopping the growth of bacteria.

This antibiotic treats only bacterial infections. It will not work for viral infections (e. g. common cold. flu ). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.

This medication should not be used in infants younger than 1 month old (see also Precautions section). This drug should not be used to treat infections outside the bladder (e. g. kidney infections such as pyelonephritis or perinephric abscesses).

How to use Macrobid

Take this medication by mouth with food, usually twice daily in the morning and evening or as directed by your doctor. Swallow the medication whole for best results.

Do not use magnesium trisilicate-containing antacids while taking this medication. These antacids can bind with nitrofurantoin. preventing its full absorption into your system.

Antibiotics work best when the amount of medicine in your body is kept at a constant level. Therefore, take this drug at evenly spaced intervals.

Continue to take this medication until the full prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may allow bacteria to continue to grow, which may result in a return of the infection.

Inform your doctor if your condition persists or worsens.

Side Effects

Nausea. headache may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

This medication may cause your urine to turn dark yellow or brown in color. This is usually a harmless, temporary effect and will disappear when the medication is stopped. However, dark brown urine can also be a sign of rare side effects (liver problems or anemia ). Therefore, seek immediate medical attention if you notice dark urine along with any of the following symptoms: persistent nausea/vomiting. stomach /abdominal pain. yellowing eyes /skin. tiredness, fast/pounding heartbeat.

Tell your doctor right away if any of these rare but very serious side effects occur: eye pain. vision changes, mental/mood changes, persistent/severe headaches. new signs of infection (e. g. fever, persistent sore throat ), easy bruising/bleeding.

Seek immediate medical attention if you develop the following rare but very serious side effects: numbness/tingling of the hands/feet, unusual muscle weakness .

This medication may rarely cause very serious (possibly fatal) lung problems. Lung problems may occur within the first month of treatment or after long-term use of nitrofurantoin (generally for 6 months or longer). Get medical help right away if you develop symptoms of lung problems, including: persistent cough. chest pain. shortness of breath/trouble breathing. joint/muscle pain. bluish/purplish skin.

This medication may rarely cause a severe intestinal condition (Clostridium difficile - associated diarrhea ) due to a resistant bacteria. This condition may occur during treatment or even weeks to months after treatment has stopped. Do not use anti-diarrhea products or narcotic pain medications if you have the following symptoms because these products may make them worse. Tell your doctor right away if you develop: persistent diarrhea, abdominal or stomach pain/cramping, blood /mucus in your stool.

Use of nitrofurantoin for prolonged or repeated periods may result in oral thrush or a new vaginal yeast infection. Contact your doctor if you notice white patches in your mouth. a change in vaginal discharge. or other new symptoms.

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction. including: rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking nitrofurantoin, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: kidney disease (e. g. little or no urine output), a certain genetic condition (G-6-PD deficiency), a history of liver problems due to nitrofurantoin use in the past.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: liver disease, lung disease, numbness/tingling of the arms/legs, vitamin B deficiency, mineral imbalance, blood disorders (e. g. anemia), diabetes, persistent weakness due to long-term disease, certain eye disorders (e. g. optic neuritis ).

Kidney function declines as you grow older. This medication is removed by the kidneys. Therefore, older adults may be at a greater risk for side effects while using this drug, especially nerve, liver or lung problems (see Side Effects section).

During pregnancy, this medication should be used only when clearly needed. It must not be used if you are near the end of your pregnancy (38-42 weeks), or at the time of labor and delivery. Doing so may cause a certain blood disorder (hemolytic anemia) in your baby. Discuss the risks and benefits with your doctor.

This medication passes into breast milk and may have undesirable effects on nursing infants younger than 1 month old or those with a certain genetic condition (G-6-PD deficiency). Consult your doctor before breast-feeding.

Interactions

(See also How to Use section).

Your healthcare professionals (e. g. doctor or pharmacist) may already be aware of any possible drug interactions and may be monitoring you for it. Do not start, stop, or change the dosage of any medicine before checking with them first.

Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use, especially: certain drugs to treat gout (uricosuric drugs such as sulfinpyrazone).

Although most antibiotics are unlikely to affect hormonal birth control such as pills, patch, or ring, a few antibiotics (such as rifampin, rifabutin) can decrease their effectiveness. This could result in pregnancy. If you use hormonal birth control, ask your doctor or pharmacist for more details.

This medication may interfere with certain laboratory tests (certain urine glucose tests), possibly causing false test results. Make sure laboratory personnel and all your doctors know you use this drug.

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center.

Notes

Do not share this medication with others.

This medication has been prescribed for your current condition only. Do not use it later for another infection unless told to do so by your doctor. A different medication may be necessary in those cases.

Laboratory and/or medical tests (e. g. kidney/liver function, blood counts/CBC, bacterial culture) should be performed periodically to monitor your progress or check for side effects. Lung function tests should be performed if you are prescribed nitrofurantoin products for extended treatment (several months or more). Consult your doctor for more details.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature between 59-86 degrees F (15-30 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Images

Amoxil Uses, Dosage - Side Effects, Ranoxyl

Amoxil

Amoxil (amoxicillin) is a penicillin antibiotic that fights bacteria.

Amoxil is used to treat many different types of infection caused by bacteria, such as tonsillitis. bronchitis. pneumonia, gonorrhea. and infections of the ear, nose, throat, skin, or urinary tract.

Amoxil is also sometimes used together with another antibiotic called clarithromycin (Biaxin) to treat stomach ulcers caused by Helicobacter pylori infection. This combination is sometimes used with a stomach acid reducer called lansoprazole (Prevacid).

Amoxil may also be used for purposes not listed in this medication guide.

Important information

Do not use Amoxil if you are allergic to amoxicillin or to any other penicillin antibiotic, such as ampicillin (Omnipen, Principen), dicloxacillin (Dycill, Dynapen), oxacillin (Bactocill), penicillin (Beepen-VK, Ledercillin VK, Pen-V, Pen-Vee K, Pfizerpen, V-Cillin K, Veetids), and others.

Before using Amoxil, tell your doctor if you are allergic to cephalosporins such as Ceclor, Ceftin, Duricef, Keflex, and others. Also tell your doctor if you have asthma, liver or kidney disease, a bleeding or blood clotting disorder, mononucleosis (also called "mono"), or any type of allergy.

Amoxil can make birth control pills less effective, which may result in pregnancy. Before taking amoxicillin, tell your doctor if you use birth control pills.

Take Amoxil for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated.

Amoxil will not treat a viral infection such as the common cold or flu. Do not give Amoxil to another person, even if they have the same symptoms you do.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. Do not use any medicine to stop the diarrhea unless your doctor has told you to.

Before taking this medicine

You should not use Amoxil if you are allergic to any penicillin antibiotic, such as ampicillin, dicloxacillin, oxacillin, penicillin, or ticarcillin.

To make sure Amoxil is safe for you, tell your doctor if you have:

liver or kidney disease;

mononucleosis (also called "mono");

a history of diarrhea caused by taking antibiotics; or

food or drug allergies (especially to a cephalosporin antibiotic such as Omnicef, Cefzil, Ceftin, Keflex, and others).

If you are being treated for gonorrhea, your doctor may also have you tested for syphilis, another sexually transmitted disease.

Amoxil is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment.

Amoxicillin can make birth control pills less effective. Ask your doctor about using non hormonal birth control (condom, diaphragm with spermicide) to prevent pregnancy while taking Amoxil.

Amoxicillin can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

The Amoxil chewable tablet may contain phenylalanine. Talk to your doctor before using this form of amoxicillin if you have phenylketonuria (PKU).

How should I take Amoxil?

Take Amoxil exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Take this medicine at the same time each day.

You may need to shake Amoxil liquid well just before you measure a dose. Follow the directions on your medicine label.

Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one. You may place the liquid directly on the tongue, or you may mix it with water, milk, baby formula, fruit juice, or ginger ale. Drink all of the mixture right away. Do not save any for later use.

The chewable tablet should be chewed before you swallow it.

While using Amoxil, you may need frequent blood tests. Your kidney and liver function may also need to be checked.

If you are taking Amoxil with clarithromycin and/or lansoprazole to treat stomach ulcer, use all of your medications as directed. Read the medication guide or patient instructions provided with each medication. Do not change your doses or medication schedule without your doctor's advice.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Amoxil will not treat a viral infection such as the flu or a common cold.

Do not share this medicine with another person, even if they have the same symptoms you have.

This medicine can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using Amoxil.

Store at room temperature away from moisture, heat, and light.

You may store liquid Amoxil in a refrigerator but do not allow it to freeze. Throw away any liquid that is not used within 14 days after it was mixed at the pharmacy.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include confusion, behavior changes, a severe skin rash, urinating less than usual, or seizure (black-out or convulsions).

What should I avoid while taking Amoxil?

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop using Amoxil and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Amoxil side effects

Get emergency medical help if you have any of these signs of an allergic reaction to Amoxil: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

diarrhea that is watery or bloody;

fever, swollen gums, painful mouth sores, pain when swallowing, skin sores, cold or flu symptoms, cough, trouble breathing;

swollen glands, rash or itching, joint pain, or general ill feeling;

pale or yellowed skin, yellowing of the eyes, dark colored urine, fever, confusion or weakness;

severe tingling, numbness, pain, muscle weakness;

easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin; or

severe skin reaction - fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common Amoxil ide effects may include:

stomach pain, nausea, vomiting, diarrhea;

vaginal itching or discharge;

swollen, black, or "hairy" tongue.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Amoxil?

Other drugs may interact with amoxicillin, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

More about Amoxil (amoxicillin)

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about Amoxil.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this Amoxil only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 9.05. Revision Date: 2016-07-22, 8:38:25 AM.

Drug Status

Heinix, Heinix

Heinix

Suomen suosituin allergialääke*

Heinix-tablettien vaikuttava aine setiritsiini on nopeavaikutteinen ja tehokas antihistamiini.

Heinix-tabletteja käytetään allergisen kausiluonteisen tai ympärivuotisen nuhan, silmäoireiden ja iho-oireiden hoitoon.

Heinix 10 mg saatavilla 10 ja 30 tabletin pakkauksissa apteekista ilman reseptiä.

Annostus:

Aikuiset ja yli 12-vuotiaat: yksi tabletti vuorokaudessa

Lapset 6-12 vuotta: yksi tabletti vuorokaudessa tai puoli tablettia kahdesti vuorokaudessa.

Alle 30-kiloiset lapset: puoli tablettia kerran vuorokaudessa.

Heinix-tabletteja ei saa käyttää alle 6-vuotiaille lapsille

Keskustele lääkärisi kanssa, jos sinulla on munuaissairaus tai olet raskaana. Vältä Heinix-tablettien käyttöä, jos imetät. Tutustu huolellisesti pakkausselosteeseen. Heinix on lääke.

Valmisteyhteenveto ja pakkausseloste (linkki Fimean lääkehakuun):

*IMS Health OTC MAT 3/2015

Haltran Advanced Patient Information, Haltran

Haltran (Oral)

Oral route(Tablet;Suspension;Capsule, Liquid Filled;Tablet, Chewable)

NSAIDs may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may be increased in patients with cardiovascular disease or risk factors for cardiovascular disease. Ibuprofen is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery. NSAIDs can also cause an increased risk of serious gastrointestinal adverse events especially in the elderly, including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal .

Commonly used brand name(s)

Actiprofen

Advil Children's

Advil Pediatric

Children's Motrin

Children's Motrin Berry Flavor

Children's Motrin Bubble Gum Flavor

Children's Motrin Grape Flavor

Equate Children's Ibuprofen - Berry

Equate Children's Ibuprofen - Berry - Dye Free

Infants' Motrin

Personnelle Children's Ibuprofen - Berry

Personnelle Children's Ibuprofen - Grape

Available Dosage Forms:

Suspension

Tablet

Capsule, Liquid Filled

Tablet, Chewable

Capsule

Therapeutic Class: Analgesic

Pharmacologic Class: NSAID

Chemical Class: Propionic Acid (class)

Uses For Haltran

Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID) used to treat mild to moderate pain, and helps to relieve symptoms of arthritis (osteoarthritis, rheumatoid arthritis, or juvenile arthritis), such as inflammation, swelling, stiffness, and joint pain. This medicine does not cure arthritis and will help you only as long as you continue to take it .

In addition, ibuprofen can be used to treat fever, menstrual cramps, and other conditions as determined by your doctor .

This medicine is available both over-the-counter (OTC) and with your doctor's prescription .

Before Using Haltran

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

Appropriate studies have not been performed on the relationship of age to the effects of ibuprofen in children below 6 months of age. Safety and efficacy have not been established .

Geriatric

Appropriate studies performed to date have not demonstrated geriatrics-specific problems that would limit the usefulness of ibuprofen in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require adjustment of dosage in patients receiving ibuprofen .

Pregnancy

Kentera, Kentera

Kentera

Previous name: Oxybutynin Nicobrand Active Substance: oxybutynin Common Name: oxybutynin ATC Code: G04BD04 Marketing Authorisation Holder: Nicobrand Ltd. Active Substance: oxybutynin Status: Authorised Authorisation Date: 2004-06-15 Therapeutic Area: Urinary Incontinence, Urge Pharmacotherapeutic Group: Urologicals

Therapeutic Indication

Symptomatic treatment of urge incontinence and/or increased urinary frequency and urgency as may occur in adult patients with unstable bladder.

What is Kentera?

Kentera is a medicine that contains the active substance oxybutynin. It is available as a transdermal patch (a patch that delivers a medicine across the skin) and as a gel in a sachet or a metering pump.

What is Kentera used for?

Kentera is used to treat urge incontinence (sudden lack of control over urination), increased urinary frequency (need to urinate frequently) and urgency (sudden urge to pass urine) in adults with an overactive bladder (when the bladder muscles contract suddenly).

The medicine can only be obtained with a prescription.

How is Kentera used?

For the transdermal patches, one patch is used twice a week (every three to four days). The patch should be applied to dry, intact skin on the abdomen (tummy), hip, or buttock immediately after it is removed from the protective sachet. A new application site should be chosen for each new patch so that the same area of skin is not used more than once within a week.

For the gel, the recommended daily dose is 4 mg of oxybutynin once a day, which corresponds to one gram of gel delivered using a metering pump or to the content of one sachet. The gel is applied to dry, intact skin on the abdomen, upper arm, shoulders or thighs. Different application sites should be chosen, so that the same area of skin is not used on consecutive days.

How does Kentera work?

The active substance in Kentera, oxybutynin, is an anticholinergic medicine. It blocks some receptors in the body called muscarinic M1 and M3 receptors. In the bladder, this causes the muscles that push urine out of the bladder to relax. This leads to an increase in the amount of urine that the bladder can hold, and to changes in the way the bladder muscles contract as the bladder fills up. This helps Kentera to prevent unwanted urination. Oxybutynin has been available as a tablet for the treatment of overactive bladder since the 1970s.

How has Kentera been studied?

Kentera transdermal patches were studied in a total of 881 patients, mostly elderly women, with overactive bladders in two main studies. In one study, they were compared with placebo (a dummy treatment) in 520 patients. In the other, they were compared with tolterodine capsules (another medicine used to treat urge incontinence) in 361 patients. The main measure of effectiveness was the number of incontinence episodes over either three or seven days.

Kentera gel was compared with placebo in one main study in 789 patients with overactive bladders. The main measure of effectiveness was the change in the number of daily incontinence episodes after 12 weeks of treatment.

What benefit has Kentera shown during the studies?

Kentera was more effective than placebo. After 12 weeks, the average number of incontinence episodes per week had decreased by 19 (about three per day) with Kentera patches, compared with a decrease of 15 episodes with placebo. Kentera patches were as effective as tolterodine, with both treatments decreasing the number of episodes by about three per day.

In the study on the gel, after 12 weeks the average number of daily incontinence episodes, which was initially at 5.4, was reduced by 2.7 episodes per day in patients receiving Kentera gel compared with a drop on average of 2 episodes per day in patients receiving placebo.

What is the risk associated with Kentera?

The most common side effects with Kentera patches (seen in more than 1 patient in 10) are application site reactions (including itching around the site of patch application). The most commonly reported side effect with Kentera gel is dry mouth (seen in between 1 and 10 patients in 100). For the full list of all side effects reported with Kentera, see the package leaflet.

Kentera should not be used in people who may be hypersensitive (allergic) to oxybutynin or any of the other ingredients. It must not be used in patients with urinary retention (difficulty in passing urine), severe gastro-intestinal conditions (problems with the stomach and gut), uncontrolled narrow-angle glaucoma (increased eye pressure even with treatment) or myasthenia gravis (a disease of the nerves and muscles causing muscle weakness), or in patients at risk of these conditions.

Why has Kentera been approved?

The CHMP had first evaluated Kentera transdermal patches and concluded that their effectiveness was similar to that of the oxybutynin tablets already on the market and that the benefits outweighed the risks. The Committee recommended that the Kentera patch be given marketing authorisation.

During its assessment of the application for Kentera gel, the CHMP concluded that its effectiveness was similar to that of the previously approved patches. The Committee therefore decided that the benefits of Kentera gel also outweighed its risks and recommended the approval of the new formulation.

Other information about Kentera

The European Commission granted a marketing authorisation valid throughout the European Union for Kentera on 15 June 2004.

For more information about treatment with Kentera, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Source: European Medicines Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

oxybutynin

They are produced using its proprietary Kentera polymer and process, which is designed to integrate the nanotubes into the plastics.

Indeed, rats fed with vanadium for 2 months developed pulmonary hypertension and right ventricular hypertrophy (Susic and Kentera 1986).

Part of the Total Chemicals group, Arkema not only supplies tubes to Zyvex, but also has a license to use Zyvex's Kentera dispersion technology and is exclusive distributor in Europe of NanoSolve products.

John ``The Coach'' Kentera. XTRA-AM (690) weeknights: His radio career continues to defy logic.

tie) Dennis McKnight and John Kentera. XTRA weeknights; Dave Smith and Ben Maller, AM-1150 weeknights: There is no battle of wits in this late-night radio war, only another reason to beg KROQ to fire up ``Love Line'' a few hours earlier each night.

Zyvex's patented and trade-secret-protected Kentera processing technology solves three key problems for CNTs; getting a good dispersion, exfoliating bundles of tubes, and adhering the CNTs to a host polymer matrix without damaging them.

John Kentera. XTRA weeknights: ``The coach,'' once known around the XTRA offices as ``the janitorial engineer,'' may claim to know Xs and Os.

Horrible mention: John Kentera (XTRA late night); John Chelesnik (XTRA); Stu Lantz (KLAC Lakerline); Ralph Lawler (KMPC Clipper talk).

Loren Roth, MD, MPH, Associate Senior Vice Chancellor for Health Sciences, University of Pittsburgh -- Web-based Technologies, ASPs, and Electronic Patient Records -- Amy Kentera. MPH, CIO Liberty Management Group -- Dennis Morrison, CEO, Center for Behavioral Health -- Thomas H.

Common Side Effects Of Norplant (Levonorgestrel Implants (Unavailable In Us)) Drug Center, Norplant

Prescribing Information

Last reviewed on RxList 10/05/2015

Norplant System (levonorgestrel ) Implants is a hormonal contraceptive used to prevent pregnancy. Common side effects of Norplant include headache, nervousness, anxiety, nausea, vomiting, dizziness, rash, acne, changes in appetite, weight gain, scalp hair loss, prolonged menstrual bleeding, and spotting, missed menstrual periods, irregular onsets of menstrual bleeding, scanty menstrual bleeding, pain or itching near the implant site (usually temporary), infection at implant site, nervousness, anxiety, breast pain. and uterine enlargement.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Norplant FDA Prescribing Information: Side Effects (Adverse Reactions)

SIDE EFFECTS

The following adverse reactions have been associated with the NORPLANT (levonorgestrel implants (unavailable in us)) SYSTEM during the first year of use in clinical trials :

Many bleeding days or prolonged bleeding

Betaval-N, Betaval-N

Duomycin

In some countries, this medicine may only be approved for veterinary use.

Found in: Switzerland

Duomycin is NOT known to be marketed in the USA. Duomycin may be available in the countries listed above.

Generic/rINN (Recommended International Nonproprietary Name)

ATC (Anatomical Therapeutic Chemical Classification)

CAS registry number (Chemical Abstracts Service)

Chemical Name

Other Brand Names

Amacin

Anasilpiel

Antibioptal

Apolar-N

Atebemyxine

Bac Neo Poly

Bacimycin

Bacitracin-Neomycin-Polymyxin

Baneocin

Baramycin

Berbesolone F

Berloson-N

Bestflan

Betason-N

Betaval-N

Betnesol-N

Betnevate N

Betnovate-N

Bevalex

Bevason

Bimixin

Bio Delta Cortilen

Bioderm

Bioplacenton

Biosol

Bivacyn

Bravoderm-N

Calf meal

Cebemyxine

Celestonvalerat

Chlomy-P

Cicatrin

Cilinafosal Neomicina

Cinolon-N

Cloxagel

CNF Scour-diet

Colimy Foam

Coliriocilina Prednisona

Colivet

Compomix

Concatag

Concentrat

Cortexiline

Cortidexason comp.

Cortikan

Cortizeme

Cysto-Myacyne

Denomix

Dentargle F

Dermamycin

Dermoran F

Desalfa

Desamix Neomicina

Desolex-N

Dexagrane

Dexapolcort N

Dexavetaderm

Diarcap

Dispadex comp.

Doricum

Ecoval

Emorex N Berna

Endomycin

Enteran

Enterocoli

Enteromicina

Enterostop

Entocunimycine

Escar-T

Eta Biocortilen

Fasolon

Fast Powder

Flucort F

Fludroxyl

Fluocort-N

FML-Neo

Forticillin

Fradiomycin

Fradiomycin Celludent

Framykoin

Francetin T

Furafenicol Vet

Halciderm Combi

Hydeltrone

Hydrocortiderm

Hydrocortisel

Hysetin P

Hyspan

Izoneocol

Jenomycin

Kalcinol-N

Kataval

Kenacort A con Neomicina

Kenacort AG

Leuco Hubber

Lincocin forte

Lincocin Neo

Lincocine

Locacorten

Mammaneopen

Mastalone

Mastalone Blue

Mastijet

Mastitar

Mastrinal

Maxitrol

Menaderm

Menaderm Neomicina

Metaskin-N

Myacyne

Myciguent

Mycitracin

Myneocin

Myrosone

Mytaderm

N B Topical

Naseptin

Nebacetin

Neo

Neo Cortef

Neo Delta Cortef

Neo Franvet

Neo Hubber

Neo Mastitar

Neo Medrol EE

Neo Predef

Neo Sol

Neo synalar

Neo Terramycin

Neo-Bacin

Neo-Flucort

Neo-Fradin

Neo-Hydro

Neo-M-Salbe

Neo-Rx

Neo-Sulcin

Neobacin

Neobacitracine

Neobiotic

Neocin

Neocina

Neoclox

Neocones

Neocortic

Neoderm

Neodex

Neoject

Neomas

Neomed

Neomicina

Neomicina L. CH.

Neomix

Neomy

Neomycane

Neomycin and Polymyxin B Sulfate

Neomycin Penicillin

Neomycin Sulfate

Neomycin-Penicillin

Neomycine Avitec

Neomycine Diamant

Neomycine Franvet

Neomycine Hydrocortisone

Neomycinesulfaat

Neomycinesulfaat CF

Neomycinsulfat

Neomycinum

Neomydiar

Neopen

Neopenol

Neopharm

Neoral

Neosel

Neosinol

Neosol

Neosporin

Neosporin Irrigating Solution

Neosulf

Neotracin

Neoxyne

Nisagon

Nivemycin

NP8

NPA Euterschutz

NPS Vetag

Nufacort

Ocemycine

Oftalmolosa Cusi Prednisona Neomicina

Ophtalkan

Ophthalmo-Framykoin

Ophthalmyvet

Optiprime

Optisone

Oregan

Orojet

Pamycon

Panolog

Parkesteron

Pimafucort

Pivalone compositum

Polyspectran Salbe

Polyspectran Tropfen

Predniderm

Predsol-N

Prevotec

Pulvo 47

Rilexine

Salmocoli

Skizon-N

Special Formula 17900 Forte V

Speciorlac

Spersapolymyxin

Statrol

Sulfintestin Neomicina

Super-Mastitar

Synalar-N

Tabernil Cria

Tarivet

Tevemyxine

Tisuderma

Topocin

Tracetin

Traital

Trefurcan

Tricin

Triple Antibiotic Ointment

Tyrothricin Provita comp.

Unguentum Neomycini

Uro-Nebacetin

Vagicillin

Vetropolycin

Vonapen

Vonapen Retard

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Betnovate helps to reduce the redness, itching, and swelling of skin conditions such as eczema, psoriasis, contact dermatitis, and seborrhea.

Use Betnovate as directed by your doctor.

This medication is usually applied 2 or 3 times daily or according to the instruction. Enough medication should be applied to completely cover the affected area with a thin film. The medication should be gently and thoroughly massaged into the affected area. In certain conditions, the doctor will order the application to be covered with a dressing. Ask your health care provider any questions you may have about how to use Betnovate.

Drug Class and Mechanism

Betnovate is a corticosteroid that is used for the topical treatment of skin irritations.

If you miss a dose, take it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one.

Store Betnovate at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Betnovate out of the reach of children and away from pets.

Betnovate should not be taken by anyone who:

is allergic to betamethasone valerate or any of the ingredients of the medication; has chickenpox; has fungal, yeast, or viral skin lesions; has herpes simplex; has tuberculosis of the skin; has vaccinia.

Possible Side Effects

Side effects that you should report to your prescriber or health care professional as soon as possible:

burning or itching of the skin; dark red spots on the skin; infection; lack of healing of the skin condition; painful, red, pus-filled blisters in hair follicles; severe burning and continued itching of the skin; thinning of the skin, with easy bruising, sunburn more likely especially on the face. Other serious side effects can develop if you use Betnovate for a long time, or if you use too much. Contact your prescriber or health care professional if you notice any unusual effects.

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): burning, itching, or irritation of the skin; dry skin; increased redness or scaling of the skin.

Betnovate is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Amoxicat Ohne Rezept, Amoxicat

Augmentin ohne rezept

Augmentin is used for treating infections caused by certain bacteria. Augmentin is a penicillin antibiotic. It works by killing sensitive bacteria.

Use Augmentin as directed by your doctor.

Take Augmentin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

To clear up your infection completely, take Augmentin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Augmentin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Augmentin.

Store Augmentin at or below 77 degrees F (25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Augmentin out of the reach of children and away from pets.

Active Ingredient: Amoxicillin/clavulanate potassium.

Do NOT use Augmentin if:

you are allergic to any ingredient in Augmentin or another penicillin antibiotic (eg, ampicillin)

you have a history of liver problems or yellowing of the eyes or skin caused by Augmentin

you have infectious mononucleosis (mono)

you are taking a tetracycline antibiotic (eg, doxycycline)

you have recently received or will be receiving live oral typhoid vaccine.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Augmentin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of allergies, asthma, hay fever, or hives

if you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness) to a cephalosporin (eg, cephalexin) or another beta-lactam antibiotic (eg, imipenem)

if you have kidney problems or gonorrhea

if you have a history of liver problems or yellowing of the eyes or skin.

Some medicines may interact with Augmentin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin) because the risk of bleeding may be increased

Probenecid because it may increase the amount of Augmentin in your blood

Chloramphenicol, macrolide antibiotics (eg, erythromycin), sulfonamides (eg, sulfamethoxazole), or tetracycline antibiotics (eg, doxycycline) because they may decrease Augmentin's effectiveness

Methotrexate because the risk of its side effects may be increased by Augmentin

Live oral typhoid vaccine or hormonal birth control (eg, birth control pills) because their effectiveness may be decreased by Augmentin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Augmentin 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.

Important safety information:

Augmentin may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Augmentin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Augmentin only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Augmentin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Augmentin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Augmentin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

Brown, yellow, or gray tooth discoloration has occurred rarely in some patients taking Augmentin. It occurred most often in children. The discoloration was reduced or removed by brushing or dental cleaning in most cases. Contact your doctor if you experience this effect.

Diabetes patients - Augmentin may cause the results of some tests for urine glucose to be wrong. Ask your doctor before you change your diet or the dose of your diabetes medicine.

Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed if you use Augmentin for a long period of time. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Augmentin with caution in the elderly; they may be more sensitive to its effects, especially patients with kidney problems.

Use Augmentin with extreme caution in children younger than 10 years old who have diarrhea or an infection of the stomach or bowel.

Augmentin should not be used in children who weigh less than 88 lbs (40 kg); safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Augmentin while you are pregnant. Augmentin is found in breast milk. If you are or will be breast-feeding while you use Augmentin, check with your doctor. Discuss any possible risks to your baby.

More Information About Cefaclor, Cefager

More information about Cefaclor

Contraindications

Hypersensitivity to cefaclor, any component of the formulation, or other cephalosporins

Warnings/Precautions

Modify dosage in patients with severe renal impairment. Prolonged use may result in superinfection. Use with caution in patients with a history of penicillin allergy especially IgE-mediated reactions (eg, anaphylaxis, urticaria). Beta-lactamase-negative, ampicillin-resistant (BLNAR) strains of H. influenzae should be considered resistant to cefaclor. Extended release tablets are not approved for use in children <16 years of age.

Adverse Reactions

Dermatologic: Rash (maculopapular, erythematous, or morbilliform) (1% to 2%)

Gastrointestinal: Diarrhea (3%)

Genitourinary: Vaginitis (2%)

Hematologic: Eosinophilia (2%)

Hepatic: Transaminases increased (3%)

Miscellaneous: Moniliasis (2%)

<1%: Agitation, agranulocytosis, anaphylaxis, angioedema, aplastic anemia, arthralgia, cholestatic jaundice, CNS irritability, confusion, dizziness, hallucinations, hemolytic anemia, hepatitis, hyperactivity, insomnia, interstitial nephritis, nausea, nervousness, neutropenia, paresthesia, pruritus, pseudomembranous colitis, PT prolonged, seizure, serum-sickness, somnolence, Stevens-Johnson syndrome, urticaria, thrombocytopenia, toxic epidermal necrolysis, vomiting

Reactions reported with other cephalosporins include fever, abdominal pain, superinfection, renal dysfunction, toxic nephropathy, hemorrhage, cholestasis

Overdosage/Toxicology

Symptoms of overdose include diarrhea, epigastric distress, nausea, and vomiting. Many beta-lactam containing antibiotics have the potential to cause neuromuscular hyperirritability or seizures. Hemodialysis may be helpful to aid in removal of the drug from blood; otherwise, treatment is supportive and symptom-directed.

Drug Interactions

Aminoglycosides: May be additive to nephrotoxicity.

Furosemide: May be additive to nephrotoxicity.

Probenecid: May decrease cephalosporin elimination.

Ethanol/Nutrition/Herb Interactions

Food: Cefaclor serum levels may be decreased slightly if taken with food. The bioavailability of cefaclor extended release tablets is decreased 23% and the maximum concentration is decreased 67% when taken on an empty stomach.

Stability

Store at controlled room temperature. Refrigerate suspension after reconstitution. Discard after 14 days. Do not freeze.

Mechanism of Action

Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis. Bacteria eventually lyse due to ongoing activity of cell wall autolytic enzymes (autolysins and murein hydrolases) while cell wall assembly is arrested.

Pharmacodynamics/Kinetics

Absorption: Well absorbed, acid stable

Distribution: Widely throughout the body and reaches therapeutic concentration in most tissues and body fluids, including synovial, pericardial, pleural, peritoneal fluids; bile, sputum, and urine; bone, myocardium, gallbladder, skin and soft tissue; crosses placenta; enters breast milk

Protein binding: 25%

Metabolism: Partially hepatic

Half-life elimination: 0.5-1 hour; prolonged with renal impairment

Time to peak: Capsule: 60 minutes; Suspension: 45 minutes

Excretion: Urine (80% as unchanged drug)

Dosage

Children >1 month: Dosing range: 20-40 mg/kg/day divided every 8-12 hours; maximum dose: 1 g/day

Otitis media: 40 mg/kg/day divided every 12 hours

Pharyngitis: 20 mg/kg/day divided every 12 hours

Adults: Dosing range: 250-500 mg every 8 hours

Extended release tablets:

Acute bacterial exacerbations of or secondary infections with chronic bronchitis: 500 mg every 12 hours for 7 days

Pharyngitis, tonsillitis, uncomplicated skin and skin structure infections: 375 mg every 12 hours for 10 days

Dosing adjustment in renal impairment:

Clcr 10-50 mL/minute: Administer 50% to 100% of dose

Clcr<10 mL/minute: Administer 50% of dose

Hemodialysis: Moderately dialyzable (20% to 50%)

Administration

Administer around-the-clock to promote less variation in peak and trough serum levels.

Chewable tablet: Should be chewed before swallowing; should not be swallowed whole

Extended release tablet: Should not be cut, crushed, or chewed; should be administered with food

Oral suspension: Shake well before using.

Monitoring Parameters

Assess patient at beginning and throughout therapy for infection; monitor for signs of anaphylaxis during first dose

Test Interactions

Positive direct Coombs', false-positive urinary glucose test using cupric sulfate (Benedict's solution, Clinitest ®. Fehling's solution), false-positive serum or urine creatinine with Jaffe reaction

Dietary Considerations

Capsule, chewable tablet, and suspension may be taken with or without food. Extended release tablet should be taken with food. Raniclor™ contains phenylalanine 2.8 mg/cefaclor 125 mg.

Patient Education

Inform prescriber of all prescriptions, OTC medications, or herbal products you are taking, and any allergies you have. Do not take any new medication during therapy unless approved by prescriber. Take as directed, at regular intervals around-the-clock (with or without food). Chilling oral suspension improves flavor (do not freeze). Do not chew or crush extended release tablets. Maintain adequate hydration (2-3 L/day of fluids) unless instructed to restrict fluid intake. Complete full course of medication, even if you feel better. May cause false test results with Clinitest ® ; use of another type of testing is preferable. May cause diarrhea (yogurt, boiled milk, or buttermilk may help). Report rash; respiratory difficulty or swallowing; persistent nausea, vomiting, or abdominal pain; changes in urinary pattern or pain on urination; opportunistic infection (eg, vaginal itching or drainage; sores in mouth; blood in stool or urine, vaginal itching or drainage, unusual fever or chills); or CNS changes (eg, irritability, agitation, nervousness, insomnia, hallucinations). Breast-feeding precaution: Consult prescriber if breast-feeding.

Dental Health: Effects on Dental Treatment

No significant effects or complications reported

Dental Health: Vasoconstrictor/Local Anesthetic Precautions

No information available to require special precautions

Dental Comment

Patients allergic to penicillins can use a cephalosporin; the incidence of cross-reactivity between penicillins and cephalosporins is 1% when the allergic reaction to penicillin is delayed. Cefaclor is effective against anaerobic bacteria, but the sensitivity of alpha-hemolytic Streptococcus vary; approximately 10% of strains are resistant. Nearly 70% are intermediately sensitive. If the patient has a history of immediate reaction to penicillin, the incidence of cross-reactivity is 20%; cephalosporins are contraindicated in these patients.

Mental Health: Effects on Mental Status

May cause nervousness; case reports of euphoria, delusion, illusions, and depersonalization with cephalosporins

Mental Health: Effects on Psychiatric Treatment

May rarely cause neutropenia; use caution with clozapine and carbamazepine

Dosage Forms

Capsule (Ceclor ® ): 250 mg, 500 mg

Powder for oral suspension: 125 mg/5 mL (75 mL, 150 mL); 187 mg/5 mL (50 mL, 100 mL); 250 mg/5 mL (75 mL, 150 mL); 375 mg/5 mL (50 mL, 100 mL)

Ceclor ®. 125 mg/5 mL (150 mL); 187 mg/5 mL (100 mL); 250 mg/5 mL (75 mL, 150 mL); 375 mg/5 mL (100 mL)

Tablet, chewable (Raniclor™): 125 mg [contains phenylalanine 2.8 mg; fruity flavor], 187 mg [contains phenylalanine 4.2 mg; fruity flavor], 250 mg [contains phenylalanine 5.6 mg; fruity flavor], 375 mg [contains phenylalanine 8.4 mg; fruity flavor]

Tablet, extended release (Ceclor ® CD): 375 mg, 500 mg

References

American Thoracic Society, "Guidelines for the Initial Management of Adults With Community-Acquired Pneumonia: Diagnosis, Assessment of Severity, and Initial Antimicrobial Therapy," Am Rev Respir Dis . 1993, 148(5):1418-26.

Boguniewicz M and Leung DYM, "Hypersensitivity Reactions to Antibiotics Commonly Used in Children," Pediatr Infect Dis J . 1995, 14(3):221-31.

Donowitz GR and Mandell GL, "Beta-Lactam Antibiotics," N Engl J Med . 1988, 318(7):419-26 and 318(8):490-500.

Hyslop DL, "Cefaclor Safety Profile: A Ten Year Review," Clin Ther . 1988, 11(Suppl A):83-94.

Levine LR, "Quantitative Comparison of Adverse Reactions to Cefaclor vs Amoxicillin in a Surveillance Study," Pediatr Infect Dis . 1985, 4(4):358-61.

Marshall WF and Blair JE, "The Cephalosporins," Mayo Clin Proc . 1999, 74(2):187-95.

Saxon A, Beall GN, Rohr AS, et al, "Immediate Hypersensitivity Reactions to Beta-Lactam Antibiotics," Ann Intern Med . 1987, 107(2):204-15.

Smith GH, "Oral Cephalosporins in Perspective," DICP . 1990, 24(1):45-51.

Wright AJ, "The Penicillins," Mayo Clin Proc . 1999, 74(3):290-307.

International Brand Names

Adco-Cefaclor ® (ZA); Alfacet ® (YU); Alfatil ® (FR); Altaclor ® (IT); Apo-Cefaclor ® (CA, PL); Bactigram ® (IT); Biocef ® (BD); Capabiotic ® (ID); CEC ® (AT, CZ, DE, DO, LU, RO, ZA); Ceclodyne ® (RO); Ceclor ® (AT, AU, BD, BE, BR, CA, CH, CO, CR, CZ, DO, ES, GT, HN, HR, HU, ID, IL, LU, MX, NL, NZ, PA, PL, PT, RO, RU, SI, SV, TR, ZA); Ceclorbeta ® (DE); Cecloretta ® (HU); Ceclor ® MR (RO); Cefabac ® (BG, JO, KW, LB, MA, MY, SY); Cefaclor 1A Pharma ® (DE); Cefaclor ABC ® (IT); Cefaclor acis ® (DE); Cefaclor Ahimsa ® (AR); Cefaclor AL ® (DE); Cefaclor AZU ® (DE); Cefaclor Basics ® (DE); Cefaclor beta ® (DE); Cefaclor Bexal ® (ES); Cefaclor Biochemie ® (CO, RO); Cefaclor ® (CZ, GB, RO); Cefaclor DOC ® (IT); Cefaclor EG ® (IT); Cefaclor Fabra ® (AR); Cefaclor Heumann ® (DE); Cefaclor K24 ® (IT); Cefaclor Lindo ® (DE); Cefaclor Merck ® (IT); Cefaclor MK ® (CR, DO, GT, HN, PA, SV); Cefaclor Normon ® (ES); Cefaclor PB ® (DE); Cefaclor Pliva ® (IT); Cefaclor Ranbaxy ® (ES); Cefaclor-ratiopharm ® (DE, HU, IT); Cefaclor Richet ® (AR); Cefaclor S250 Stada ® (TH); Cefaclor Sandoz ® (DE); Cefaclor Stada ® (DE); Cefaclor-Teva ® (IL); Cefaclor-Wolff ® (DE); CefaCl ® (SI); Cefager ® (IE); Cefahexal ® (AT); Cefaklor ® (YU); Cefalcor ® (IT); Cefalor ® (IL); Cefaltrex ® (DO); Cefamid ® (DO); Cefastad ® (AT); Cef-Diolan ® (DE); Cefin ® (DO); Cefkor ® (AU); Cefor ® (PL); Cefral ® (AR); Cefulton ® (IT); CEK ® (PL); Celco ® (TH); cephaclor von ct ® (DE); Cephalodoc ® (DE); Citiclor ® (IT); Cleancef ® (SG); Cloracef ® (HK, ID, JO, KW, LB, MT, MY, RO, ZA); Clorad ® (IT); Clorazer ® (IT); Clorotir ® (NZ); DBL Cefaclor ® (AU); Distaclor ® (GB, HK, IE, SG, TH); Dista MR ® (GB); Doccefaclo ® (BE); Dorf ® (IT); Especlor ® (ID); Eurocefix ® (IT); Faclor ® (BR); Falcef ® (DO); Fuclode ® (IT); Geniclor ® (IT); hefa clor ® (DE); Infectocef ® (DE); Kefaclor ® (TH); Keflor ® (AU, CL, IN); Kefolor ® (FI); Kefsid ® (TR); Keftid ® (GB, IE); Kliacef ® (IT); Kloracef ® (PL); KWICap ® (AR); Lafarclor ® (IT); Lilly-Cefaclor ® (ZA); Loracef ® (BD); Losefar ® (TR); Medikoncef ® (ID); Medoclor ® (RO); Navacef ® (BD); Necloral ® (IT); Novacef ® (BR); Novo-Cefaclor (CA); Nu-Cefaclor (CA); Oralcef ® (IT); Panacef ® (IT); Panclor ® (PL); Panoral ® (DE); Performer ® (IT); Pinaclor ® (IE); PMS-Cefaclor (CA); Razicef ® (BG); Remeclor ® (CY); Rolab-Cefaclor ® (ZA); Selviclor ® (IT); Serviclor ® (CZ, PL); Sifaclor ® (TH); Sigacefal ® [caps.] (DE); Sinclor ® (RO); Soficlor ® (SG); Suclor ® (DO); Taracef ® (PL, RU, SI); Tibifor ® (IT); Vercef ® (CZ, HU, PL, RO, RU, SG, TH, ZA); Vercef MR ® (CZ, HU, PL)

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Search For All Records, Epinat

Bournaud, Frederic ; Renaud, Florent ; Daddi, Emanuele ; Duc, Pierre-Alain ; Elbaz, David ; Gabor, Jared M. ; Juneau, Stephanie ; Kraljic, Katarina ; Le Floch', Emeric ; Perret, Valentin ; et al

Star-forming disk galaxies at high redshift are often subject to violent disk instability, characterized by giant clumps whose fate is yet to be understood. The main question is whether the clumps disrupt within their dynamical timescale (?50 Myr), like the molecular clouds in today's galaxies, or whether they survive stellar feedback for more than a disk orbital time (?300 Myr) in which case they can migrate inward and help building the central bulge. We present 3.5-7 pc resolution adaptive mesh refinement simulations of high-redshift disks including photoionization, radiation pressure, and supernovae feedback. Our modeling of radiation pressure determines the massmore » loading and initial velocity of winds from basic physical principles. We find that the giant clumps produce steady outflow rates comparable to and sometimes somewhat larger than their star formation rate, with velocities largely sufficient to escape the galaxy. The clumps also lose mass, especially old stars, by tidal stripping, and the stellar populations contained in the clumps hence remain relatively young (?200 Myr), as observed. The clumps survive gaseous outflows and stellar loss, because they are wandering in gas-rich turbulent disks from which they can reaccrete gas at high rates compensating for outflows and tidal stripping, overall keeping realistic and self-regulated gaseous and stellar masses. The outflow and accretion rates have specific timescales of a few 10 yr, as opposed to rapid and repeated dispersion and reformation of clumps. Our simulations produce gaseous outflows with velocities, densities, and mass loading consistent with observations, and at the same time suggest that the giant clumps survive for hundreds of Myr and complete their migration to the center of high-redshift galaxies. These long-lived clumps are gas-dominated and contain a moderate mass fraction of stars; they drive inside-out disk evolution, thickening, spheroid growth, and fueling of the central black hole. « less

RESONANT STRUCTURE IN THE DISKS OF SPIRAL GALAXIES, USING PHASE REVERSALS IN STREAMING MOTIONS FROM TWO-DIMENSIONAL H FABRY-PEROT SPECTROSCOPY

Font, Joan ; Beckman, John E. ; Fathi, Kambiz ; Gutierrez, Leonel ; Epinat, BenoIt ; Hernandez, Olivier, E-mail: jfont@iac. es, E-mail: jeb@iac. es, E-mail: benoit. epinat@ast. obs-mip. fr, E-mail: kambiz@astro. su. se, E-mail: leonel@astrosen. unam. mx, E-mail: hernandez@astro. umontreal. ca

In this Letter, we introduce a technique for finding resonance radii in a disk galaxy. We use a two-dimensional velocity field in H emission obtained with Fabry-Perot interferometry, derive the classical rotation curve, and subtract it off, leaving a residual velocity map. As the streaming motions should reverse sign at corotation, we detect these reversals and plot them in a histogram against galactocentric radius, excluding points where the amplitude of the reversal is smaller than the measurement uncertainty. The histograms show well-defined peaks which we assume to occur at resonance radii, identifying corotations as the most prominent peaks corresponding tomore » the relevant morphological features of the galaxy (notably bars and spiral arm systems). We compare our results with published measurements on the same galaxies using other methods and different types of data. « less

Bournaud, Frederic ; Renaud, Florent ; Daddi, Emanuele ; Duc, Pierre-Alain ; Elbaz, David ; Gabor, Jared M. ; Juneau, Stephanie ; Kraljic, Katarina ; Le Floch', Emeric ; Perret, Valentin ; et al

Star-forming disk galaxies at high redshift are often subject to violent disk instability, characterized by giant clumps whose fate is yet to be understood. The main question is whether the clumps disrupt within their dynamical timescale (?50 Myr), like the molecular clouds in today's galaxies, or whether they survive stellar feedback for more than a disk orbital time (?300 Myr) in which case they can migrate inward and help building the central bulge. We present 3.5-7 pc resolution adaptive mesh refinement simulations of high-redshift disks including photoionization, radiation pressure, and supernovae feedback. Our modeling of radiation pressure determines the massmore » loading and initial velocity of winds from basic physical principles. We find that the giant clumps produce steady outflow rates comparable to and sometimes somewhat larger than their star formation rate, with velocities largely sufficient to escape the galaxy. The clumps also lose mass, especially old stars, by tidal stripping, and the stellar populations contained in the clumps hence remain relatively young (?200 Myr), as observed. The clumps survive gaseous outflows and stellar loss, because they are wandering in gas-rich turbulent disks from which they can reaccrete gas at high rates compensating for outflows and tidal stripping, overall keeping realistic and self-regulated gaseous and stellar masses. The outflow and accretion rates have specific timescales of a few 10 yr, as opposed to rapid and repeated dispersion and reformation of clumps. Our simulations produce gaseous outflows with velocities, densities, and mass loading consistent with observations, and at the same time suggest that the giant clumps survive for hundreds of Myr and complete their migration to the center of high-redshift galaxies. These long-lived clumps are gas-dominated and contain a moderate mass fraction of stars; they drive inside-out disk evolution, thickening, spheroid growth, and fueling of the central black hole. « less

RESONANT STRUCTURE IN THE DISKS OF SPIRAL GALAXIES, USING PHASE REVERSALS IN STREAMING MOTIONS FROM TWO-DIMENSIONAL H FABRY-PEROT SPECTROSCOPY

Font, Joan ; Beckman, John E. ; Fathi, Kambiz ; Gutierrez, Leonel ; Epinat, BenoIt ; Hernandez, Olivier, E-mail: jfont@iac. es, E-mail: jeb@iac. es, E-mail: benoit. epinat@ast. obs-mip. fr, E-mail: kambiz@astro. su. se, E-mail: leonel@astrosen. unam. mx, E-mail: hernandez@astro. umontreal. ca

In this Letter, we introduce a technique for finding resonance radii in a disk galaxy. We use a two-dimensional velocity field in H emission obtained with Fabry-Perot interferometry, derive the classical rotation curve, and subtract it off, leaving a residual velocity map. As the streaming motions should reverse sign at corotation, we detect these reversals and plot them in a histogram against galactocentric radius, excluding points where the amplitude of the reversal is smaller than the measurement uncertainty. The histograms show well-defined peaks which we assume to occur at resonance radii, identifying corotations as the most prominent peaks corresponding tomore » the relevant morphological features of the galaxy (notably bars and spiral arm systems). We compare our results with published measurements on the same galaxies using other methods and different types of data. « less

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