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บริการดูแลรักษาผู้ป่วยด้วยประสบกาณ์ และคิดค้นตัวยา เพื่อบริการรักษาอาการเจ็บป่วยตลอดมา โรคหลายชนิดสามารถรักษาให้หายได้ เพียงท่านไว้ใจเรา พวกเราก็เต็มที่ ไม่เลี้ยงไข้ พวกเรา หมอและทีมงานขอขอบคุณทุกท่านที่มาเยี่ยมชมเว็บไซต์เป็นอย่างสูง | บริการปรึกษา ปัญหา
บริการดูแลรักษาผู้ป่วยด้วยประสบกาณ์ และคิดค้นตัวยา เพื่อบริการรักษาอาการเจ็บป่วยตลอดมา โรคหลายชนิดสามารถรักษาให้หายได้ เพียงท่านไว้ใจเรา พวกเราก็เต็มที่ ไม่เลี้ยงไข้ พวกเรา หมอและทีมงานขอขอบคุณทุกท่านที่มาเยี่ยมชมเว็บไซต์เป็นอย่างสูง | บริการปรึกษา ปัญหา
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3 reasons why women with postmenopausal osteoporosis at high risk for fracture choose Prolia®. IMPORTANT SAFETY INFORMATION: DO NOT TAKE PROLIA® IF YOU: have low blood calcium; or are pregnant or plan to become pregnant, as Prolia® may harm your unborn baby; or are allergic to denosumab or any ingredients in Prolia®. WHAT IS THE MOST IMPORTANT INFORMATION I SHOULD KNOW ABOUT PROLIA®? If you receive Prolia®, you should not receive XGEVA®. Prolia® contains the same medicine as XGEVA® (denosumab). PROLIA® CAN CAUSE SERIOUS SIDE EFFECTS: SERIOUS ALLERGIC REACTIONS have happened in people who take Prolia®. Call your doctor or go to your nearest emergency room right away if you have any symptoms of a serious allergic reaction, including low blood pressure (hypotension); trouble breathing; throat tightness; swelling of your face, lips, or tongue; rash; itching; or hives. LOW BLOOD CALCIUM (HYPOCALCEMIA). Prolia® may lower the calcium levels in your blood. If you have low blood calcium, it may get worse during treatment. Your low blood calcium must be treated before you receive Prolia®. Take calcium and vitamin D as your doctor tells you to help prevent low blood calcium. SEVERE JAW BONE PROBLEMS (OSTEONECROSIS) may occur. Your doctor should examine your mouth before you start Prolia® and may tell you to see your dentist. It is important for you to practice good mouth care during treatment with Prolia®. UNUSUAL THIGH BONE FRACTURES. Some people have developed unusual fractures in their thigh bone. Symptoms of a fracture include new or unusual pain in your hip, groin, or thigh. INCREASED RISK OF BROKEN BONES, INCLUDING BROKEN BONES IN THE SPINE, AFTER STOPPING, SKIPPING OR DELAYING PROLIA®. Talk with your doctor before starting Prolia® treatment. After your treatment with Prolia® is stopped, or if you skip or delay taking a dose, your risk for breaking bones, including bones in your spine, is increased. Your risk for having more than 1 broken bone in your spine is increased if you have already had a broken bone in your spine. Do not stop, skip or delay taking Prolia® without first talking with your doctor. If your Prolia® treatment is stopped, talk to your doctor about other medicine that you can take. SERIOUS INFECTIONS in your skin, lower stomach area (abdomen), bladder, or ear may happen. Inflammation of the inner lining of the heart (endocarditis) due to an infection may also happen more often in people who take Prolia®. You may need to go to the hospital for treatment. Prolia® is a medicine that may affect the ability of your body to fight infections. People who have weakened immune systems or take medicines that affect the immune system may have an increased risk for developing serious infections. SKIN PROBLEMS such as inflammation of your skin (dermatitis), rash, and eczema have been reported. BONE, JOINT, OR MUSCLE PAIN. Some people who take Prolia® develop severe bone, joint, or muscle pain. BEFORE TAKING PROLIA®, TELL YOUR DOCTOR ABOUT ALL OF YOUR MEDICAL CONDITIONS, INCLUDING IF YOU: • Take the medicine XGEVA® (denosumab) • Have low blood calcium • Cannot take daily calcium and vitamin D • Had parathyroid or thyroid surgery (glands located in your neck) • Have been told you have trouble absorbing minerals in your stomach or intestines (malabsorption syndrome) • Have kidney problems or are on kidney dialysis • Are taking medicine that can lower your blood calcium levels • Plan to have dental surgery or teeth removed • Are pregnant or plan to become pregnant FEMALES WHO ARE ABLE TO BECOME PREGNANT: • Your healthcare provider should do a pregnancy test before you start treatment with Prolia®. • You should use an effective method of birth control (contraception) during treatment with Prolia® and for at least 5 months after your last dose of Prolia®. • Tell your doctor right away if you become pregnant while taking Prolia®. • Are breast-feeding or plan to breast-feed WHAT ARE THE POSSIBLE SIDE EFFECTS OF PROLIA®? It is not known if the use of Prolia® over a long period of time may cause slo
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Feeling unsteady or dizzy can be caused by many factors such as poor circulation, inner ear disease, medication usage, injury, infection, allergies, and/or neurological disease. Dizziness is treatable, but it is important for your doctor to help you determine the cause so that the correct treatment is implemented. Don't give up. Call us to find a doctor who can work with you to find the cause if your symptoms. Al Tawasul Specialized Center: +974 4402-9000 We are pleased to announce that we are admitting all patients 7 days a week. We also like to announce that we are accepting patients with the following health insurance: - Damaan Islamic Insurance Company - Beema (#Beema) - Qatar Insurance Company (QIC) (#QLM) - #Allianz -#NextCare - #Alkoot Follow us: Facebook.com/TawasulENT Instagram.com/AlTawasulCenterENT Twitter.com/TawasulENT #Qatar #Doha #Qatar_Charity #ENT #vertigo #Dizziness #Audiology #Speech_Therapy #Sinusitis #Sinus_Infection
Prolia® (denosumab) | Postmenopausal Osteoporosis Treatment
Help reduce the risk of having an osteoporosis-related fracture with Prolia®: bit.ly/PRO-PMO IMPORTANT SAFETY INFO: Do not take Prolia® if you: have low blood calcium; or are pregnant or plan to become pregnant, as Prolia® may harm your unborn baby; or are allergic to denosumab or any ingredients in Prolia®. What is the most important information I should know about Prolia®? If you receive Prolia®, you should not receive XGEVA®. Prolia® contains the same medicine as XGEVA® (denosumab). Prolia® can cause serious side effects: Serious allergic reactions have happened in people who take Prolia®. Call your doctor or go to your nearest emergency room right away if you have any symptoms of a serious allergic reaction, including low blood pressure (hypotension); trouble breathing; throat tightness; swelling of your face, lips, or tongue; rash; itching; or hives. Low blood calcium (hypocalcemia). Prolia® may lower the calcium levels in your blood. If you have low blood calcium, it may get worse during treatment. Your low blood calcium must be treated before you receive Prolia®. Take calcium and vitamin D as your doctor tells you to help prevent low blood calcium. Severe jaw bone problems (osteonecrosis) may occur. Your doctor should examine your mouth before you start Prolia® and may tell you to see your dentist. It is important for you to practice good mouth care during treatment with Prolia®. Unusual thigh bone fractures. Some people have developed unusual fractures in their thigh bone. Symptoms of a fracture include new or unusual pain in your hip, groin, or thigh. Increased risk of broken bones, including broken bones in the spine, after stopping, skipping or delaying Prolia®. Talk with your doctor before starting Prolia® treatment. After your treatment with Prolia® is stopped, or if you skip or delay taking a dose, your risk for breaking bones, including bones in your spine, is increased. Your risk for having more than 1 broken bone in your spine is increased if you have already had a broken bone in your spine. Do not stop, skip or delay taking Prolia® without first talking with your doctor. If your Prolia® treatment is stopped, talk to your doctor about other medicine that you can take. Serious infections in your skin, lower stomach area (abdomen), bladder, or ear may happen. Inflammation of the inner lining of the heart (endocarditis) due to an infection may also happen more often in people who take Prolia®. You may need to go to the hospital for treatment. Prolia® is a medicine that may affect the ability of your body to fight infections. People who have weakened immune systems or take medicines that affect the immune system may have an increased risk for developing serious infections. Skin problems such as inflammation of your skin (dermatitis), rash, and eczema have been reported. Bone, joint, or muscle pain. Some people who take Prolia® develop severe bone, joint, or muscle pain. Before taking Prolia®, tell your doctor about all of your medical conditions, including if you: • Take the medicine XGEVA® (denosumab) • Have low blood calcium • Cannot take daily calcium and vitamin D • Had parathyroid or thyroid surgery (glands located in your neck) • Have been told you have trouble absorbing minerals in your stomach or intestines (malabsorption syndrome) • Have kidney problems or are on kidney dialysis • Are taking medicine that can lower your blood calcium levels • Plan to have dental surgery or teeth removed • Are pregnant or plan to become pregnant Females who are able to become pregnant: • Your healthcare provider should do a pregnancy test before you start treatment with Prolia®. • You should use an effective method of birth control (contraception) during treatment with Prolia® and for at least 5 months after your last dose of Prolia®. • Tell your doctor right away if you become pregnant while taking Prolia®. • Are breast-feeding or plan to breast-feed What are the possible side effects of Prolia®? It is not known if the use of Prolia® over a long period of time may cause slow heal
U.S. Food and Drug Administration
For over 10 years, making a difference in the lives of people like Lib has been our inspiration. Full Prescribing Info: https://bit.ly/2pkdv0D Important Safety Info: What is the most important information I should know about Nplate®? Nplate® can cause serious side effects, including: • Worsening of a precancerous blood condition to a blood cancer (leukemia): Nplate® is not for use in people with a precancerous condition called myelodysplastic syndromes (MDS) or for any condition other than chronic (lasting a long time) immune thrombocytopenia (ITP). If you have MDS and receive Nplate®, your MDS condition may worsen and become an acute leukemia. If MDS worsens to become acute leukemia you may die sooner from the acute leukemia. • Higher risk for blood clots: - You may have a higher risk of getting a blood clot if your platelet count becomes high during treatment with Nplate®. You may have severe complications or die from some forms of blood clots, such as clots that spread to the lungs or that cause heart attacks or strokes. - If you have a chronic liver disease, you may get blood clots in the veins of your liver. This may affect your liver function. • What are the possible side effects of Nplate®? - Nplate® may cause serious side effects. See "What is the most important information I should know about Nplate®?" - The most common side effects of Nplate® in adults include: -- headache -- joint pain -- dizziness -- trouble sleeping -- muscle tenderness or weakness -- pain in arms and legs -- stomach (abdomen) pain -- shoulder pain -- indigestion -- tingling or numbness in hands and feet - The most common side effects of Nplate® in children 1 year of age and older include: -- inflammation of the passages in the nose and throat -- upper respiratory tract infection -- itchy, runny, or blocked nose -- sore throat and discomfort with swallowing -- inflammation of the eye -- ear infection -- inflammation in the lining of the intestines -- inflammation of the sinuses -- cough -- pain in mouth and throat -- upper stomach (abdomen) pain -- diarrhea -- rash -- bleeding beneath the surface of the skin or bruising under the skin -- itchy rash -- fever -- swelling in the limbs/hands/feet -- bruising - People who take Nplate® may have an increased risk of developing new or worsening changes in the bone marrow called “increased reticulin.” These changes may improve if you stop taking Nplate®. Your healthcare provider may need to check your bone marrow for this problem during treatment with Nplate®. - These are not all the possible side effects of Nplate®. Tell your healthcare provider if you have any side effect that bothers you or that does not go away. For more information, ask your healthcare provider or pharmacist. - If you have any questions about this information, be sure to discuss with your doctor. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. How will I receive Nplate®? Nplate® is given under the skin (subcutaneous injection) one time each week by your healthcare provider. Your healthcare provider will check your platelet count every week and change your dose of Nplate® as needed. This will continue until your healthcare provider decides that your dose of Nplate® can stay the same. After that, you will need to get blood tests every month. When you stop receiving Nplate®, you will need blood tests for at least 2 weeks to check if your platelet count drops too low. Pregnancy Surveillance Program: Women who become pregnant during Nplate® treatment are encoura
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