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    Strattera is an effective drug for the pharmacotherapy of attention deficit hyperactivity disorder (ADHD). Patients can buy Strattera to use it to relieve the symptoms of ADHD and comorbid disorders (depression, enuresis) in children and adults. Strattera acts on the noradrenergic system of the brain, and thus contributes to an effective relief of ADHD symptoms. Strattera provides a more favorable impact over the cognitive functions, than psychostimulants from other pharmacological groups. Strattera is prescribed only when cognitive and behavioral disorders can not be overcome with the help of non-drug therapies for ADHD – psychotherapy, behavior correction and others. This drug for alleviating the ADHD symptoms and comorbid disorders is available in two dosage forms. Both medicinal forms of Strattera can be found in the city pharmacy chains or ordered in online pharmacies. To buy Strattera in a regular pharmacy, you need a medical prescription from a psychiatrist or a psychologist with a confirmed diagnosis of ADHD. zithromax dosage for gonorrhea Drug name: Strattera Generic name: Atomoxetine Hydrochloride, Axepta Use: Attention deficit hyperactivity disorder (ADHD) Strattera is prescribed by doctors to treat patients suffering from attention deficit hyperactivity disorder (ADHD). Strattera capsules contain the active ingredient atomoxetine hydrochloride, which is a type of medicine called a selective noradrenaline re-uptake inhibitor. It works by increasing the levels of noradrenaline in the brain, which appears to reduce problems associated with ADHD, although the exact workings of the drug are unknown. Strattera is usually prescribed to patients between the ages of 6 years and 17 years. The possible Strattera side effects include: • Constipation; • Cough, dry mouth; • Feeling irritable; • Feeling dizzy or drowsy; • Increased menstrual cramps; • Impotence, loss of interest in sex; • Skin rash or itching; • Sleep problems. More serious side effects may include: • Chest pain, shortness of breath; • Feeling like you may pass out; • Increased blood pressure; • Nausea, pain in the upper stomach, itching, loss of appetite, jaundice; • Numbness, burning, tingling; • Unusual thoughts or behavior; • Urinating less than usual. Before purchasing, tell your doctor if you have any of the following medical conditions: • Any kind of heart problem or disorder; • History of stroke, blood clots or heart attack; • If any family member has died from heart attack; • Liver disease; • Problems with urination.

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    It is not often that members of one of the most successful teams in a country make significantly less than their unsuccessful counterparts. However, this is exactly the case with the two United States national soccer teams. In their Equal Employment Opportunity Commission (EEOC) complaint[1] against the United States Soccer Federation (USSF), five stars from the women’s team Alex Morgan, Carli Lloyd, Megan Rapinoe, Becky Sauerbrunn and Hope Solo stated that despite producing higher revenues than the men’s national team, the women’s team received four times less than the men’s squad.[2] The complaint was officially filed on March 29“We are the best in the world, have three World Cup Championships, four Olympic Championships, and the [U. Men’s National Team] USMNT get paid more just to show up than we get paid to win major championships.” One example of this is that the U. Women’s National Team (USWNT) made only $2 million for their dominant World Cup title run, while the USMNT made $9 million the year before they even appeared in the World Cup. Another example of the compensation disparity is shown by merit pay. USWNT players receive $1,350 per match only if they win their game. On the other side, USMNT receive $5,000 for a loss in a similar match and can make up to $17,625 for a win.[3] The EEOC complaint calls for these discrepancies to be changed and has the potential to be a turning point for equal pay in women’s sports. The EEOC complaint came as a result of the expiration of Collective Bargaining Agreement (CBA) between the USSF and the USWNT in 2012. Strattera belongs to the category of medicines known as "selective norepinephrine reuptake" inhibitors. It is used to treat attention-deficit/h2yperactivity disorder (ADHD). It is part of a complete treatment program which includes other complementary measures like social, educational and psychological treatment. It increases the level of those chemicals in nerves and brain which cause hyperactivity and impulse control. It provides relief from symptoms and regular symptom improvements thereafter, such as improvement in behavior and attention span. The Strattera drug should not be prescribed for patients who show primary psychiatric disorders and others symptoms secondary to environmental factors. It is prescribed only in cases where remedial measures alone are not sufficient and the symptoms are severe. You should not take this medication if you are allergic to Atomoxetine or suffer from glaucoma. Brand or generic Strattera must not be taken if you have used an MAO (monoamine oxidase) inhibitor like selegiline (Eldepryl, Emsam), phenelzine (Nardil), rasagiline (Azilect), isocarboxazid (Marplan), and tranylcypromine (Parnate), in the past 14 days. Using Strattera before MAO inhibitor has cleared from the body can cause life threatening side effects.

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    500 mg PO once, then 250 mg once daily for 4 days 2 g extended release suspension PO once 500 mg IV as single dose for at least 2 days; follow with oral therapy with single dose of 500 mg to complete 7-10 days course of therapy Infection of pharynx, cervix, urethra, or rectum: Ceftriaxone 250 mg IM once plus azithromycin 1 g PO once (preferred) or alternatively doxycycline 100 mg PO q12hr for 7 days CDC STD guidelines: MMWR Recomm Rep. June 5, 20(RR3);1-137 Agitation Allergic reaction Anemia Anorexia Candidiasis Chest pain Conjunctivitis Constipation Dermatitis (fungal) Dizziness Eczema Edema Enteritis Facial edema Fatigue Gastritis Headache Hyperkinesia Hypotension Increased cough Insomnia Leukopenia Malaise Melena Mucositis Nervousness Oral candidiasis Pain Palpitations Pharyngitis Pleural effusion Pruritus Pseudomembranous colitis Rash Rhinitis Seizures Somnolence Urticaria Vertigo Anaphylaxis Angioedema Anorexia Bronchospasm Constipation Dermatologic reactions Dyspepsia Elevated liver enzymes Erythema multiforme Flatulence Oral candidiasis Pancreatitis Pseudomembranous colitis Pyloric stenosis, rare reports of tongue discoloration Stevens-Johnson syndrome Torsades de pointes Toxic epidermal necrolysis Vomiting/diarrhea, rarely resulting in dehydration Neutropenia Elevated bilirubin, AST, ALT, BUN, creatinine Alterations in potassium Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Use with caution in abnormal liver function, hepatitis, cholestatic jaundice, hepatic necrosis, and hepatic failure have been reported, some of which have resulted in death; discontinue azithromycin immediately if signs and symptoms of hepatitis occur Injection-site reactions can occur with IV route In treatment of gonorrhea or syphilis, perform susceptibility culture tests before initiating azithromycin therapy; may mask or delay symptoms of incubating gonorrhea or syphilis. Bacterial or fungal superinfection may result from prolonged use Prolonged QT interval: Cases of torsades de pointes have been reported during postmarketing surveillance; use with caution in patients with known QT prolongation, history of torsades de pointes, congenital long QT syndrome, bradyarrhythmias, or uncompensated heart failure; also use with caution if coadministering with drugs that prolong QT interval or proarrhythmic conditions (eg, hypokalemia, hypomagnesemia); elderly patients may be more susceptible to drug-associated effects on QT interval Pneumonia: PO azithromycin is safe and effective only for community-acquired pneumonia (CAP) due to C pneumoniae, H influenzae, M pneumoniae, or S pneumoniae Cases of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) reported; despite successful symptomatic treatment of allergic symptoms, when symptomatic therapy was discontinued, allergic symptoms recurred soon thereafter in some patients without further azithromycin exposure; if allergic reaction occurs, the drug should be discontinued and appropriate therapy instituted; physicians should be aware that allergic symptoms may reappear when symptomatic therapy discontinued Endocarditis prophylaxis: Indicated only for high-risk patients, per current AHA guidelines Use caution in renal impairment (Cr Cl Because of the low levels of azithromycin in breastmilk and use in infants in higher doses, it would not be expected to cause adverse effects in breastfed infants (Lact Med; https://nih.gov/newtoxnet/lactmed.htm) Binds to 50S ribosomal subunit of susceptible microorganisms and blocks dissociation of peptidyl t RNA from ribosomes, causing RNA-dependent protein synthesis to arrest; does not affect nucleic acid synthesis Concentrates in phagocytes and fibroblasts, as demonstrated by in vitro incubation techniques; in vivo studies suggest that concentration in phagocytes may contribute to drug distribution to inflamed tissues Y-site: Amikacin, aztreonam, cefotaxime, ceftazidime, ceftriaxone, cefuroxime, ciprofloxacin, clindamycin, droperidol, famotidine, fentanyl, furosemide, gentamicin, imipenem, cilastatin, ketorolac, levofloxacin, morphine, piperacillin-tazobactam, ondansetron(? ), potassium chloride, ticarcillin-clavulanate, tobramycin The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information. Zithromax, Zmax azithromycin dosing, indications, interactions. amoxicillin taste Zithromax - FDA The Trusted Provider of Medical Information since 1899
     
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