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Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) |
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Anti Depressants » Other » Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) is a complex of three different closely related aminoglycoside sulfates Gentamicins C1 C2 and C1(subA) obtained from Micromonospora purpurea and related species. They are broad-spectrum antibiotics but may cause ear and kidney damage. They act to inhibit protein synthesis (genetic translation). Buy Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) and other Other products online at Medstore. Buy Online at Medstore - Click Here!
About Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate): Product Type: Other Brand name: Diprogenta Generic name: Betamethasone Dipropionate + Gentamicin Sulfate What is Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? Gentamicin is an antibiotic. It fights bacteria in the body. Gentamicin is used to treat severe or serious bacterial infections. Gentamicin may also be used for purposes other than those listed in this medication guide. What is the most important information I should know about Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? If you are injecting Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) at home your healthcare provider will give you detailed instructions on how and where to inject the medication. If you do not understand these directions do not attempt to inject the medication. Contact your healthcare provider for further instructions. Gentamicin may cause damage to the kidneys and/or nerves. Kidney function and drug levels in the blood may be monitored with blood tests during treatment. Tell your doctor if you experience hearing loss dizziness numbness skin tingling muscle twitching or seizures which may be signs of nerve damage. What should I discuss with my healthcare provider before using Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? Do not use Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) without first talking to your doctor if you have • sulfite sensitivity; • kidney disease; • hearing loss or loss of balance due to ear problems; • Parkinson's disease; or • a neuromuscular disorder such as myasthenia gravis. You may not be able to use Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above. Do not use Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) without first talking to your doctor if you are pregnant or could become pregnant during treatment. Do not use Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) without first talking to your doctor if you are breast-feeding a baby. How should I take Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? If you are injecting Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) at home your healthcare provider will give you detailed instructions on how and where to inject the medication. If you do not understand these directions do not attempt to inject the medication. Contact your healthcare provider for further instructions. Do not use any Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) that is discolored has particles in it or looks different from your previous doses. Throw away any unused Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) after the amount of time determined by your pharmacist or doctor. Adequate hydration is important during treatment with Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate). Fluids may be administered intravenously during treatment. It is important that the medication be given on a regular schedule and for the entire amount of time prescribed by your doctor. Gentamicin may cause damage to the kidneys and/or nerves. Kidney function and drug levels in the blood may be monitored with blood tests during treatment. Tell your doctor if you experience hearing loss dizziness numbness skin tingling muscle twitching or seizures which may be signs of nerve damage. Dispose of used needles and syringes in a puncture resistant container out of the reach of children. Your healthcare provider will store Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) as directed by the manufacturer or give you detailed storage instructions if you are storing the medication at home. What happens if I miss a dose? Contact your doctor if a dose is missed. What happens if I overdose? Contact your doctor or seek emergency medical attention if an overdose is suspected. An overdose of the medication may result in damage to the kidneys or hearing loss dizziness numbness skin tingling muscle twitching or seizures (which may be signs of nerve damage). What should I avoid while taking Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? There are no restrictions on food beverages or activity while taking Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) unless otherwise directed by your doctor. Gentamicin side effects If you experience any of the following serious side effects stop taking Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) and seek emergency medical attention: • an allergic reaction (shortness of breath; closing of the throat; hives; swelling of the lips face or tongue; rash; or fainting); • little or no urine; • decreased hearing or ringing in the ears; • dizziness clumsiness or unsteadiness; • numbness skin tingling muscle twitching or seizures; or • severe watery diarrhea and abdominal cramps. Other less serious side effects may be more likely to occur. Continue to take Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) and talk to your doctor if you experience • increased thirst; • loss of appetite; • nausea or vomiting; • a rash. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. What other drugs will affect Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate)? Other drugs especially those that affect the kidneys can interact with Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) resulting in dangerous side effects and/or decreased effectiveness. Do not take any other prescription or over-the-counter medicines including vitamins minerals and herbal products without first talking to your doctor during treatment with Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate). Generic Diprogenta (Betamethasone Dipropionate + Gentamicin Sulfate) Alcomicin Apogen Bristagen Cidomycin Diprogen G-Mycin G-Myticin Garamycin Garamycin Otic Solution Garasone Ophthalmic Ointment Genoptic Liquifilm Genoptic S.O.P. Gentacidin Gentafair Gentak Gentamar Jenamicin Lupider G Ocu-Mycin Otomax Ointment Sandoz Pentasone Septopal Spectro-Genta Topagen U-gencin Valisone G 0.05/0.1% 10g 10 tubes 0.05/0.1% 10g 15 tubes 0.05/0.1% 10g 25 tubes 0.05/0.1% 10g 20 tubes 0.05/0.1% 10g 5 tubes Betamethasone Dipropionate + Gentamicin Sulfate Diprogenta
View more Other Anti Depressants: Anafranil (Clomipramine HCI) Anafranil (Clomipramine HCI) is a tricyclic antidepressant used to treat depression and obsessive-compulsive disorder. Buy Anafranil (Clomipramine HCI) and other Anti Depressants products online at Medstore. About Anafranil (Clomipramine HCI): Product Type: Anti Depressants Brand name: Anafranil Generic name: Clomipramine HCI What is the most important information I should know about Anafranil? • While you are taking Anafranil you may need to be monitored for worsening symptoms of depression and/ or suicidal thoughts at the start of therapy or when doses are changed. This concern about the increased risk of suicidal thoughts or behaviors may be greater if you are 18 years of age or younger and are taking Anafranil. In patients younger than 18 years the period of risk may extend beyond start of therapy or when doses are changed. Your doctor may want you to monitor for the following symptoms: anxiety panic attacks difficulty sleeping irritability hostility impulsivity severe restlessness and mania (mental and/ or physical hyperactivity). These symptoms may be associated with the development of worsening symptoms of depression and/ or suicidal thoughts or actions. Contact your healthcare provider if you develop any new or worsening mental health symptoms during treatment with Anafranil. Do not stop taking Anafranil. • It may be 4 weeks or more before you start to feel better but do not stop taking Anafranil without first talking to your doctor. • Use caution when driving operating machinery or performing other hazardous activities. Anafranil may cause drowsiness or dizziness. If you experience drowsiness or dizziness avoid these activities. • Dizziness is likely to occur when you rise from a sitting or lying position. Rise slowly to prevent dizziness and a possible fall. • Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while you are taking Anafranil. What is Anafranil? • Anafranil is in a class of drugs called tricyclic antidepressants. Anafranil affects chemicals in the brain that may become unbalanced and cause obsessive-compulsive disorder. • Anafranil is used to relieve symptoms of obsessive-compulsive disorder such as recurrent thoughts or feelings and repetitive actions. • Anafranil may also be used for purposes other than those listed in this medication guide. What should I discuss with my healthcare provider before taking Anafranil? • Do not take Anafranil if you have taken a monoamine oxidase inhibitor such as isocarboxazid (Marplan) phenelzine (Nardil) or tranylcypromine (Parnate) within the last 14 days. • Before taking Anafranil tell your doctor if you have liver disease kidney disease asthma thyroid disease diabetes stomach or intestinal problems high blood pressure or heart disease had a heart attack in the last 6 weeks an enlarged prostate or difficulty urinating glaucoma or seizures. • You may not be able to take Anafranil or you may require a dosage adjustment or special monitoring during therapy if you have any of the conditions listed above. • While you are taking Anafranil you may need to be monitored for worsening symptoms of depression and/ or suicidal thoughts at the start of therapy or when doses are changed. This concern about the increased risk of suicidal thoughts or behaviors may be greater if you are 18 years of age or younger and are taking Anafranil. In patients younger than 18 years the period of risk may extend beyond start of therapy or when doses are changed. Your doctor may want you to monitor for the following symptoms: anxiety panic attacks difficulty sleeping irritability hostility impulsivity severe restlessness and mania (mental and/ or physical hyperactivity). These symptoms may be associated with the development of worsening symptoms of depression and/ or suicidal thoughts or actions. Contact your healthcare provider if you develop any new or worsening mental health symptoms during treatment with Anafranil. Do not stop taking Anafranil. • Anafranil is in the FDA pregnancy category C. This means that it is not known whether Anafranil will harm an unborn baby. Do not take Anafranil without first talking to your doctor if you are pregnant or could become pregnant during treatment. • Anafranil passes into breast milk and may affect a nursing baby. Do not take Anafranil without first talking to your doctor if you are breast-feeding a baby. How should I take Anafranil? • Take Anafranil exactly as directed by your doctor. If you do not understand these directions ask your pharmacist nurse or doctor to explain them to you. • Take each dose with a full glass (8 oz) of water. • Anafranil may be taken several times a day or in one daily dose (usually at bedtime). Follow your doctor's instructions. • Grapefruit and grapefruit juice may interact with Anafranil. The interaction could lead to potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor. • It may be 4 weeks or more before you start to feel better but do not stop taking Anafranil without first talking to your doctor. • Store Anafranil at room temperature away from moisture and heat. What happens if I miss a dose? • Take the missed dose as soon as you remember. If it is almost time for the next regularly scheduled dose skip the missed dose and take the next one as directed. Do not take a double dose of this medication unless otherwise directed by your doctor. What happens if I overdose? • Seek emergency medical attention. • Symptoms of a Anafranil overdose include seizures confusion drowsiness agitation hallucinations and low blood pressure (dizziness fatigue fainting). What should I avoid while taking Anafranil? • Use caution when driving operating machinery or performing other hazardous activities. Anafranil may cause drowsiness or dizziness. If you experience drowsiness or dizziness avoid these activities. • Dizziness is likely to occur when you rise from a sitting or lying position. Rise slowly to prevent dizziness and a possible fall. • Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while you are taking Anafranil. • Grapefruit and grapefruit juice may interact with Anafranil. The interaction could lead to potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor. • Do not stop taking Anafranil suddenly. This could cause symptoms such as nausea headache and malaise. What are the possible side effects of Anafranil? • If you experience any of the following serious side effects stop taking Anafranil and contact your doctor immediately or seek emergency medical treatment: an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips face or tongue; or hives); seizures; a fast or irregular heartbeat; a heart attack; high blood pressure (blurred vision severe headache); difficulty urinating; or fever with increased sweating muscle stiffness or severe muscle weakness. • Other less serious side effects may be more likely to occur. Continue to take Anafranil and talk to your doctor if you experience drowsiness or dizziness; dry mouth and eyes; constipation; mild tremor; sweating; mild agitation weakness or headache; ringing in the ears; nausea; or loss of weight or appetite. • Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. What other drugs will affect Anafranil? • Do not take Anafranil if you have taken a monoamine oxidase inhibitor such as isocarboxazid (Marplan) phenelzine (Nardil) or tranylcypromine (Parnate) within the last 14 days. • Anafranil may increase the effects of other drugs that cause drowsiness including other antidepressants alcohol antihistamines sedatives (used to treat insomnia) pain relievers anxiety medicines and muscle relaxants. Tell your doctor about all medicines that you are taking and do not take any other prescription or over-the-counter medicines without first talking to your doctor. • Drugs other than those listed here may also interact with Anafranil. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines including herbal products. 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