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Postmarketing reports: Palpitations[Ref]

FLOVENT HFA 44 mcg Inhalation Aerosol, FLOVENT HFA 110 mcg Inhalation Aerosol, and FLOVENT HFA 220 mcg Inhalation Aerosol are pressurized metered-dose aerosol units fitted with a counter. FLOVENT HFA is intended for oral inhalation only. Each unit contains a microcrystalline suspension of fluticasone propionate (micronized) in propellant HFA-134a (1,1,1,2-tetrafluoroethane). It contains no other excipients.

insomnia or trouble sleeping. LAMICTAL can cause serious rashes requiring hospitalization and discontinuation of treatment. The incidence of these rashes, which have included Stevens-Johnson syndrome, is approximately 0.8% (8 per 1,000) in pediatric patients (aged 2 to 16 years) receiving LAMICTAL as adjunctive therapy for epilepsy and 0.3% (3 per 1,000) in adults on adjunctive therapy for epilepsy. In clinical trials of bipolar and other mood disorders, the rate of serious rash was 0.08% (0.8 per 1,000) in adult patients receiving LAMICTAL as initial monotherapy and 0.13% (1.3 per 1,000) in adult patients receiving LAMICTAL as adjunctive therapy. In a prospectively followed cohort of 1,983 pediatric patients (aged 2 to 16 years) with epilepsy taking adjunctive LAMICTAL, there was 1 rash-related death. In worldwide postmarketing experience, rare cases of toxic epidermal necrolysis and/or rash-related death have been reported in adult and pediatric patients, but their numbers are too few to permit a precise estimate of the rate.

Most Important Fact about Diclofenac Sodium EC You should have frequent checkups with your doctor if you take Diclofenac Sodium EC regularly. Ulcers or internal bleeding can occur without warning. Diclofenac Sodium EC precautions if you are pregnant or breastfeeding Do not take Diclofenac Sodium EC late in your pregnancy; it could harm the baby. Check with your doctor before taking Diclofenac Sodium EC early in pregnancy; it should be used only if necessary. Diclofenac Sodium EC does appear in breast milk and could affect a nursing infant. If Diclofenac Sodium EC is essential to your health, your doctor may advise you to discontinue breastfeeding until your treatment with it is finished. Special warnings about Diclofenac Sodium EC Diclofenac Sodium EC may cause dizziness and so may affect your ability to drive or operate machinery safely. Do not drive or operate machinery until you know how Diclofenac Sodium EC affects you and you are sure it won\'t affect your performance. People with impaired kidney, liver or heart function who are taking Diclofenac Sodium EC should have their kidney function monitored. During long-term treatment, routine blood tests are recommended to monitor kidney function, liver function and levels of blood components, particularly in the elderly. Diclofenac Sodium EC may mask the signs and symptoms of infection. This may make you think mistakenly that an infection is getting better when it isn\'t, or that an infection is less serious than it is. For this reason you should tell your doctor if you get an infection while you are taking Diclofenac Sodium EC. It is important that people with a history of disorders affecting the stomach or intestines are closely monitored by a doctor while taking Diclofenac Sodium EC, particularly if elderly. Consult your doctor immediately if you experience side effects such as stomach pain, indigestion, heartburn or signs of bleeding in the stomach or intestines, eg blood in the stools, while taking Diclofenac Sodium EC. Close medical supervision is important in people suffering from severe impairment of liver function. changes in your menstrual cycle,

Uncommon (0.1% to 1%): Grade 3 rash (vesiculation, moist desquamation, ulceration), grade 4 rash (erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, necrosis requiring surgery, exfoliative dermatitis)

Metformin hydrochloride Does this medicine have any possible side effects WARNING: Cyclosporine is a drug that reduces the body's ability to fight illness/disease (an immunosuppressant), leaving patients vulnerable to infection or other problems (including cancers such as lymphoma). Using other drugs that treat organ transplant rejection along with this drug may increase these tendencies. Cyclosporine can also cause high blood pressure and kidney problems. The risk of both problems increases with higher doses and longer treatment with this drug. Psoriasis patients who have had certain previous treatments (e.g., coal tar, methotrexate, PUVA, UVB, or other radiation therapy) are at increased risk to develop skin cancer. Therefore, cyclosporine must be given only under close medical supervision. Because different brands deliver different amounts of medication, do not switch brands of cyclosporine without your doctor's permission and directions. Laboratory tests (e.g., kidney function tests, blood tests) may be performed to monitor your progress.