Drug deutsch

drug deutsch

Übersetzung für 'drug' im kostenlosen Englisch-Deutsch Wörterbuch von LANGENSCHEIDT – mit Beispielen, Synonymen und Aussprache. Englisch-Deutsch-Übersetzungen für to drug im Online-Wörterbuch unab.nu ( Deutschwörterbuch). Viele übersetzte Beispielsätze mit "drug" – Deutsch-Englisch Wörterbuch und Suchmaschine für Millionen von Deutsch-Übersetzungen.

Drug Deutsch Video

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To view content sources and attributions, please refer to our editorial policy. We comply with the HONcode standard for trustworthy health information - verify here.

Try the Pill Identifier Quickly identify pills, tablets and capsules using the web's most comprehensive Pill Identification Wizard.

Featured Tool Worried about drug interactions? Use the Interactions Checker The drug interactions tool allows you to check for drug-drug and drug-food interactions.

Featured Tool Discover treatment options with the Symptom Checker This interactive decision guide helps identify the underlying cause of common symptoms.

Featured Tool Custom search for Medical Transcriptionists? Primatene Mist Primatene Mist epinephrine is an over-the-counter OTC bronchodilator used for the temporary relief of the symptoms of mild asthma.

Udenyca Udenyca pegfilgrastim-cbqv is a leukocyte growth factor biosimilar to Neulasta pegfilgrastim indicated to reduce the duration of More new drug approvals.

Drugs in Development Not yet approved. Yupelri Yupelri revefenacin is an investigational long-acting muscarinic antagonist LAMA in development for the treatment of chronic More new drug applications.

Study Treatments for "tennis elbow" are generally ineffective, researchers say, but don't despair: Posted today in Medical Health Tip: Symptoms of Kidney Stones -- Kidney stones are hard masses that form in the urinary tract, and can cause very painful symptoms if they become stuck and difficult to pass.

Warning Signs of Carpal Tunnel Syndrome -- Carpal tunnel syndrome occurs when the nerve that runs from the forearm to the wrist becomes squeezed or compressed.

Increases in Yoga, Meditation for Children in The use of yoga and meditation have increased in recent years among children and adults, while use of chiropractors has also increased among adults, according to two November data briefs published by the U.

Cold urticaria Familial Primary cold contact urticaria Secondary cold contact urticaria Reflex cold urticaria. Heat urticaria Localized heat contact urticaria Solar urticaria.

Dermatographic urticaria Vibratory angioedema Pressure urticaria Cholinergic urticaria Aquagenic urticaria.

Acquired C1 esterase inhibitor deficiency Adrenergic urticaria Exercise urticaria Galvanic urticaria Schnitzler syndrome Urticaria-like follicular mucinosis.

Episodic angioedema with eosinophilia Hereditary angioedema. Erythema multiforme minor Erythema multiforme major Stevens—Johnson syndrome , Toxic epidermal necrolysis panniculitis Erythema nodosum Acute generalized exanthematous pustulosis.

Erythema annulare centrifugum Erythema marginatum Erythema migrans Erythema gyratum repens. Necrolytic migratory erythema Erythema toxicum Erythroderma Palmar erythema Generalized erythema.

Aldrich-Mees' lines Beau's lines Muehrcke's lines Terry's nails. Hypersensitivity and autoimmune diseases Atopic eczema Allergic urticaria Allergic rhinitis Hay fever Allergic asthma Anaphylaxis Food allergy common allergies include: Hemolytic disease of the newborn.

Graves' disease Myasthenia gravis Pernicious anemia. Henoch—Schönlein purpura Hypersensitivity vasculitis Reactive arthritis Farmer's lung Post-streptococcal glomerulonephritis Serum sickness Arthus reaction.

Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis. Allergic contact dermatitis Mantoux test. Diabetes mellitus type 1 Hashimoto's thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis.

Transfusion-associated graft versus host disease. Drug reactions YY59 , EE Penicillin drug reaction Sulfonamide hypersensitivity syndrome Urticarial erythema multiforme Adverse effects of fluoroquinolones hormones: Steroid acne Steroid folliculitis chemotherapy: Chemotherapy-induced acral erythema Chemotherapy-induced hyperpigmentation Scleroderma-like reaction to taxanes Hydroxyurea dermopathy Exudative hyponychial dermatitis blood: Anticoagulant-induced skin necrosis Warfarin necrosis Vitamin K reaction Texier's disease anticonvulsant: Allopurinol hypersensitivity syndrome pulmonary: Leukotriene receptor antagonist-associated Churg—Strauss syndrome vaccine: Eczema vaccinatum other specified agents: Adverse reaction to biologic agents Adverse reaction to cytokines Bromoderma Halogenoderma Iododerma Red man syndrome Methotrexate-induced papular eruption unspecified agent: Acute generalized exanthematous pustulosis Bullous drug reaction Drug-induced acne Drug-induced angioedema Drug-related gingival hyperplasia Drug-induced lichenoid reaction Drug-induced lupus erythematosus Drug-induced nail changes Drug-induced pigmentation Drug-induced pseudolymphoma Drug-induced urticaria Fixed drug reaction Stevens—Johnson syndrome Injection site reaction Linear IgA bullous dermatosis Toxic epidermal necrolysis HIV disease-related drug reaction Photosensitive drug reaction Serum sickness-like reaction.

Retrieved from " https: Drug eruptions Clinical pharmacology. Hypersensitivity reactions — including that cross-sensitivity may occur with other sympathomimetics.

Renal and urinary disorders Not known: Renal dysfunction, dysuria, urinary retention. This is most likely to occur in those with bladder outlet obstruction, such as prostatic hypertrophy.

Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme.

Ingestion of 5 g or more of paracetamol may lead to liver damage if the patient has risk factors see below. If the patient a: Regularly consumes ethanol in excess of recommended amounts.

Is likely to be glutathione deplete e. Symptoms Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain.

Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur.

In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema, and death.

Acute renal failure with acute tubular necrosis, strongly suggested by loin pain, haematuria and proteinuria, may develop even in the absence of severe liver damage.

Cardiac arrhythmias and pancreatitis have been reported. Treatment Immediate treatment is essential in the management of paracetamol overdose. Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention.

Symptoms may be limited to nausea or vomiting and may not reflect the severity of overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines, see BNF overdose section.

Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour. Plasma paracetamol concentration should be measured at 4 hours or later after ingestion earlier concentrations are unreliable.

Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however, the maximum protective effect is obtained up to 8 hours postingestion.

The effectiveness of the antidote declines sharply after this time. If required the patient should be given intravenous N-acetylcysteine, in line with the established dosage schedule.

If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas, outside hospital. Management of patients who present with serious hepatic dysfunction beyond 24 h from ingestion should be discussed with the NPIS or a liver unit.

Caffeine Symptoms Overdose of caffeine may result in epigastric pain, vomiting, diuresis, tachycardia or cardiac arrhythmia, CNS stimulation insomnia, restlessness, excitement, agitation, jitteriness, tremors and convulsions.

It must be noted that for clinically significant symptoms of caffeine overdose to occur with this product, the amount ingested would be associated with serious paracetamol-related liver toxicity.

Treatment No specific antidote is available, but supportive measures may be used. Phenylephrine Symptoms Phenylephrine overdosage is likely to result in effects similar to those listed under adverse reactions.

Additional symptoms may include hypertension, and possibly reflex bradycardia. In severe cases confusion, hallucinations, seizures and arrhythmias may occur.

However the amount required to produce serious phenylephrine toxicity would be greater than that required to cause paracetamol-related liver toxicity.

Treatment Treatment should be as clinically appropriate. Severe hypertension may need to be treated with alpha blocking drugs such as phentolamine.

Other cold combination preparations, paracetamol combinations ATC code: R05XA01 Paracetamol Analgesic effect: Paracetamol is most effective in relieving low intensity pain of nonvisceral origin.

Paracetamol does not have antiinflammatory effects. Paracetamol produces antipyresis by a mechanism similar to that of salicylates.

Paracetamol lowers body temperature in patients with fever but rarely lowers normal body temperature. The drug acts on the hypothalamus to produce antipyresis; heat dissipation is increased as a result of vasodilatation and increased peripheral blood flow.

Paracetamol reduces fever by inhibiting the action of endogenous pyrogen on hypothalamic heat-regulating centres. Eustachian tube function is also improved.

Caffeine Caffeine potentiates the therapeutic potential of paracetamol. A slightly positive influence of caffeine on the absorption rate of paracetamol was seen: Paracetamol is rapidly absorbed from the gastrointestinal tract, reaching peak plasma levels within 40 to 60 min.

The area under the concentration versus time curve increases proportionally with dose, indicating linearity of pharmacokinetics. Concentrations of phenylephrine increase linearly with an increase in dosage.

The accumulation index is 1. Caffeine is readily absorbed after oral administration. Maximal plasma concentrations of caffeine are achieved within 1 h.

With increasing doses AUC increases disproportionately indicating non-linear kinetics. Caffeine exhibits dosedependent pharmacokinetics. Paracetamol is rapidly and uniformly distributed into most body tissues.

Paracetamol is transferred across the placenta with an extraction ratio of 0. Paracetamol passes rapidly into milk of nursing mothers.

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Klicken Sie einfach auf ein Wort, um die Ergebnisse erneut angezeigt zu bekommen. Die auf Medikamentenmangel zurückzuführende Kindersterblichkeit hat sich verdoppelt. Anmeldung und Nutzung des Forums sind kostenlos. Zur mobilen Version wechseln. Transliteration aktiv Tastaturlayout Phonetisch.

Researchers are currently working on a vaginal ring that releases both levonorgestrel a contraceptive hormone and dapivirine an antiviral effective against HIV that can be left in place […].

Over the past two decades, we have learned a lot about vitamin D. Buying medicines online is very tempting.

Shopping from the safety of your couch in your living room seems like a great way to save time and money, particularly when these drugs are just soooooooo much cheaper than what your local drug store can offer.

The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records.

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This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. To view content sources and attributions, please refer to our editorial policy.

We comply with the HONcode standard for trustworthy health information - verify here. Try the Pill Identifier Quickly identify pills, tablets and capsules using the web's most comprehensive Pill Identification Wizard.

Featured Tool Worried about drug interactions? Use the Interactions Checker The drug interactions tool allows you to check for drug-drug and drug-food interactions.

Featured Tool Discover treatment options with the Symptom Checker This interactive decision guide helps identify the underlying cause of common symptoms.

Featured Tool Custom search for Medical Transcriptionists? Primatene Mist Primatene Mist epinephrine is an over-the-counter OTC bronchodilator used for the temporary relief of the symptoms of mild asthma.

Udenyca Udenyca pegfilgrastim-cbqv is a leukocyte growth factor biosimilar to Neulasta pegfilgrastim indicated to reduce the duration of More new drug approvals.

Drugs in Development Not yet approved. Yupelri Yupelri revefenacin is an investigational long-acting muscarinic antagonist LAMA in development for the treatment of chronic More new drug applications.

Study Treatments for "tennis elbow" are generally ineffective, researchers say, but don't despair: Posted today in Medical Health Tip: Symptoms of Kidney Stones -- Kidney stones are hard masses that form in the urinary tract, and can cause very painful symptoms if they become stuck and difficult to pass.

Warning Signs of Carpal Tunnel Syndrome -- Carpal tunnel syndrome occurs when the nerve that runs from the forearm to the wrist becomes squeezed or compressed.

Increases in Yoga, Meditation for Children in The use of yoga and meditation have increased in recent years among children and adults, while use of chiropractors has also increased among adults, according to two November data briefs published by the U.

Posted in Blog Vitamin D: Our most controversial vitamin? Similarly, drugs which promote gastric emptying such as metoclopramide and domperidone may increase the rate of paracetamol absorption.

Cholestyramine reduces the absorption of paracetamol. These interactions are considered to be of unlikely clinical significance in acute usage at the dosage regimen proposed.

Medical advice should be sought before taking paracetamol-caffeine phenylephrine in combination with the following drugs: Hypertensive interactions occur between sympathomimetic amines such as phenylephrine and monoamine Oxidase inhibitors see contraindications.

Concomitant use of phenylephrine with other sympathomimetics amines can increase the risk of cardiovascular side effects see warnings and precautions.

Phenylephrine may reduce the efficacy of beta-blocking drugs and antihypertensive drugs. The risk of hypertension and other cardiovascular side effects may be increased see contraindications.

May increase the risk of cardiovascular side effects with phenylephrine see contraindications. Concomitant use of phenylephrine with digoxin or cardiac glycosides may increase the risk of irregular heartbeat or heart attack.

Warfarin and other coumarins: The anticoagulant effect of warfarin and other coumarins may be enhanced by prolonged regular daily use of paracetamol with an increased risk of bleeding; occasional doses have no significant effect.

There is a potential increased risk of lower birth weight and spontaneous abortion associated with caffeine consumption during pregnancy.

Breastfeeding This product should not be used while breast-feeding without medical advice. Caffeine in breast milk may have a stimulating effect on breast-fed infants.

Phenylephrine may be excreted in breast milk. Especially at the start of treatment, on increasing the dose or switching medication and in conjunction with alcohol.

In this section frequencies of undesirable effects are defined as follows: Thrombocytopenia, leukopenia, agranulocytosis, pancytopenia. Immune system disorders Not known: Allergic reactions angiooedema, dyspnoea, sweating, nausea, hypotension until shock , anaphylaxis.

Cutaneous hypersensitivity reactions including skin rashes. Nervous system disorders Not known: Tiredness, headache, dizziness, insomnia, anxiety, nervousness, irritability, restlessness and excitability.

Eye disorders Not known: Worsening of a pre-existing narrow-angle glaucoma Mydriasis, acute angle closure glaucoma, most likely to occur in those with closed angle glaucoma.

Cardiac disorders Not known: Respiratory, thoracic and mediastinal disorders Not known: Gastrointestinal disorders Not known: Dry mouth, nausea, vomiting, diarrhoea, anorexia.

Hepatobiliary disorders Very rare: Skin and subcutaneous tissue disorders Very rare: Very rare cases of serious skin reactions have been reported Not known: Hypersensitivity reactions — including that cross-sensitivity may occur with other sympathomimetics.

Renal and urinary disorders Not known: Renal dysfunction, dysuria, urinary retention. This is most likely to occur in those with bladder outlet obstruction, such as prostatic hypertrophy.

Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.

Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme.

Ingestion of 5 g or more of paracetamol may lead to liver damage if the patient has risk factors see below. If the patient a: Regularly consumes ethanol in excess of recommended amounts.

Is likely to be glutathione deplete e. Symptoms Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain.

Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur.

In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema, and death. Acute renal failure with acute tubular necrosis, strongly suggested by loin pain, haematuria and proteinuria, may develop even in the absence of severe liver damage.

Cardiac arrhythmias and pancreatitis have been reported. Treatment Immediate treatment is essential in the management of paracetamol overdose.

Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention. Symptoms may be limited to nausea or vomiting and may not reflect the severity of overdose or the risk of organ damage.

Management should be in accordance with established treatment guidelines, see BNF overdose section. Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour.

Plasma paracetamol concentration should be measured at 4 hours or later after ingestion earlier concentrations are unreliable.

Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however, the maximum protective effect is obtained up to 8 hours postingestion.

The effectiveness of the antidote declines sharply after this time. If required the patient should be given intravenous N-acetylcysteine, in line with the established dosage schedule.

If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas, outside hospital.

Management of patients who present with serious hepatic dysfunction beyond 24 h from ingestion should be discussed with the NPIS or a liver unit.

Caffeine Symptoms Overdose of caffeine may result in epigastric pain, vomiting, diuresis, tachycardia or cardiac arrhythmia, CNS stimulation insomnia, restlessness, excitement, agitation, jitteriness, tremors and convulsions.

It must be noted that for clinically significant symptoms of caffeine overdose to occur with this product, the amount ingested would be associated with serious paracetamol-related liver toxicity.

Treatment No specific antidote is available, but supportive measures may be used. Phenylephrine Symptoms Phenylephrine overdosage is likely to result in effects similar to those listed under adverse reactions.

Additional symptoms may include hypertension, and possibly reflex bradycardia. In severe cases confusion, hallucinations, seizures and arrhythmias may occur.

However the amount required to produce serious phenylephrine toxicity would be greater than that required to cause paracetamol-related liver toxicity.

Treatment Treatment should be as clinically appropriate. Severe hypertension may need to be treated with alpha blocking drugs such as phentolamine.

Other cold combination preparations, paracetamol combinations ATC code: R05XA01 Paracetamol Analgesic effect: Paracetamol is most effective in relieving low intensity pain of nonvisceral origin.

Paracetamol does not have antiinflammatory effects. Paracetamol produces antipyresis by a mechanism similar to that of salicylates. Paracetamol lowers body temperature in patients with fever but rarely lowers normal body temperature.

The drug acts on the hypothalamus to produce antipyresis; heat dissipation is increased as a result of vasodilatation and increased peripheral blood flow.

Paracetamol reduces fever by inhibiting the action of endogenous pyrogen on hypothalamic heat-regulating centres. Eustachian tube function is also improved.

Caffeine Caffeine potentiates the therapeutic potential of paracetamol. A slightly positive influence of caffeine on the absorption rate of paracetamol was seen: Paracetamol is rapidly absorbed from the gastrointestinal tract, reaching peak plasma levels within 40 to 60 min.

The area under the concentration versus time curve increases proportionally with dose, indicating linearity of pharmacokinetics.

Concentrations of phenylephrine increase linearly with an increase in dosage. The accumulation index is 1. Caffeine is readily absorbed after oral administration.

Maximal plasma concentrations of caffeine are achieved within 1 h. With increasing doses AUC increases disproportionately indicating non-linear kinetics.

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