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LEVORA | Women Care | Fast Escrow Refills
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Levora is a popular drug thatcontains a great combination of several female sex hormones that are known to help in the prevention of ovulation.
Levora Information
Levora is a popular drug thatcontains a great combination of several female sex hormones that are known to help in the prevention of ovulation. This medicine is also known to cause various changes in the woman’s uterine lining and cervical mucous, thus making it harder for a fertilized egg to attach itself to the woman’s uterus. Levora is widely prescribed as a contraceptive and it is taken by woman as who want to prevent an unwanted pregnancy.
Levora Indications
Levora is a popular contraceptive method (pill) that is often taken by patients (women) who want to avoid the risk of an unwanted pregnancy. However, this drug could also be prescribed to treat or to prevent some other medical disorders that have not been mentioned here.
Levora Warnings
A treatment with this medicine during pregnancy is known to cause severe (dangerous) birth defects. It is recommended that you use an extra birth control method. If you accidentally get pregnant during your treatment with this drug, you must alert your personal doctor right away. You should wait at least one month after you have had a baby to start a treatment with this medicine. You should not start a treatment with Levora if you have:
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If you do have any of the medical disorders that have been mentioned here, you may have to take in a lower dose of Levora (or you might not be allowed to start a treatment with this medicine at all). The hormones that are found in most birth control pills are known to be able to pass into the patient’s breast milk, thus harming a nursing infant. A treatment with this drug is also known to decrease the organism’s regular milk production. You must not start a treatment with this medicine if you are currently breastfeeding a child.
A treatment with a hormone-based medicine is known to increase the patient’s (woman’s) risk of developing stroke, blood clots, heart attack or other heart disorders (especially if the patient is older than 35 year old or if she is a smoker).
Levora Intake Guidelines
Ask your personal doctor how and when you should take Levora. You must not disobey any of his or her instructions (advices). You can also rely on the instructions that are usually written on the drug’s label. If you do not understand some of these instructions, you can ask a nurse, a doctor or a pharmacist for further advice and recommendations (they should be able to explain them to you).
Levora Dosage
Ask your personal physician to tell you the proper dose of Levora that you should take during your treatment with this drug. Avoid altering the dose that he or she has prescribed you in any way without your physician’s consent. The regular dose of Levora normally consists of one pill that should be taken once each day. When you have no more tablets in your pack, buy another pack of pills and start it the following day.
Levora Overdose
If you think that you might be suffering from an overdose with this drug, you are in need for immediate medical attention. You should contact your local poison control centre as soon as you can. Inform your personal physician immediately. The average symptoms of an overdose with Levora usually include vomiting, nausea and vaginal bleeding.
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Fosamax (Alendronate) | escrowrefills.com
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Buy Fosamax from our online pharmacy. Fosamax, or Alendronate as it is otherwise known, is an Osteoporosis medication that is widely used for the treatment of bone diseases such as Osteoporosis and Paget’s disease.
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Fosamax Information
Buy Fosamax from our online pharmacy. Fosamax, or Alendronate as it is otherwise known, is an Osteoporosis medication that is widely used for the treatment of bone diseases such as Osteoporosis and Paget’s disease. Alendronate, the active component of Fosamax, is a compound that increases the bone formation and corrects bone breakdown in the body.
Medicine Intake Guidelines
Our online pharmacies state that Fosamax is a possible throat and mouth irritant. Fosamax should be taken with precaution as it might cause mouth irritation when chewed or broken down. It is advised to take Fosamax with a full glass of water (about 6-8 ounces) and to avoid chewing or breaking down the tablet as it might irritate your throat and mouth; in short, swallow the tablet whole.
Fosamax is usually prescribed for a once weekly intake. On advice from our online pharmacy, it is best to take it on the same day each week. It is also best to take this Osteoporosis medication in the morning before eating or drinking anything. The full action of Fosamax could only be felt when it is not taken along with other foods and beverages as they may greatly decrease the action of Fosamax in your body.
Fosamax Missed Dose
It is fine to miss a dose when taking Fosamax, as there are no effects on your medication and treatment when a single dose has been missed. When missing a dosage of Fosamax, just take a tablet the morning after you remember to and continue with your normal schedule of Fosamax intake after that. Remember not to take double doses when you have missed a dose of this Osteoporosis medication as it is strictly not advised.
Fosamax Overdose
Effects of Overdosage of medicine are unknown but the following symptoms could be expected when an overdose occurs:
- Nausea
- Heartburn
- Abdominal Pain
- Stomach related disorders such as cramps and diarrhea
- Uncontrollable facial grimace
- Seizures
- Irritability
- And other abnormal behavior
Fosamax Side Effects
If you experience the following discomforts when taking Fosamax, you should seek medical attention immediately
- Allergic Reactions such as breathing discomforts, closing of throat, swelling of facial body parts such as lips and tongue or the entire face.
- Chest Pains, difficulty in breathing and swallowing
- Burning Sensation in ribs and back
- Heartburn whether newly acquired or worsening condition
Fosamax Warnings
When you have other diseases aside from bone related ones, you should first seek medical advice before taking Fosamax.
Among these diseases are:
- Swallowing Problem such as narrowing of the esophagus
- Esophageal diseases such as esophageal ulcers
- Low level of calcium in the body
- Kidney Disorders
- Stomach and other Digestive Problems
- Not being able to sit and/or stand straight for a full 30 minutes as this is really essential when taking Fosamax.
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Depo Provera (Medroxyprogesterone acetate) | Women Care Medicine
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Depo-Provera (Medroxyprogesterone acetate)
Depo-Provera CI is indicated only for the prevention of pregnancy. The loss of bone mineral density (BMD) in women of all ages and the impact on peak bone mass in adolescents should be considered, along with the decrease in BMD that occurs during pregnancy and/or lactation
Prevention Of Pregnancy
Both the 1 mL vial and the 1 mL prefilled syringe of Depo-Provera CI should be vigorously shaken just before use to ensure that the dose being administered represents a uniform suspension. The recommended dose is 150 mg of Depo-Provera CI every 3 months (13 weeks) administered by deep IM injection in the gluteal or deltoid muscle. Depo-Provera CI should not be used as a long-term birth control method (i.e. longer than 2 years) unless other birth control methods are considered inadequate. Dosage does not need to be adjusted for body weight [see Clinical Studies].
To ensure the patient is not pregnant at the time of the first injection, the first injection should be given ONLY during the first 5 days of a normal menstrual period; ONLY within the first 5-days postpartum if not breast-feeding; and if exclusively breast-feeding, ONLY at the sixth postpartum week. If the time interval between injections is greater than 13 weeks, the physician should determine that the patient is not pregnant before administering the drug. The efficacy of Depo-Provera CI depends on adherence to the dosage schedule of administration.
Side Effect :-
The following important adverse reactions observed with the use of Depo-Provera CI are discussed in greater detail in the Warnings and Precautions section (5):
- Loss of Bone Mineral Density [see WARNINGS AND PRECAUTIONS]
- Thromboembolic disease [see WARNINGS AND PRECAUTIONS]
- Breast Cancer [see WARNINGS AND PRECAUTIONS]
- Anaphylaxis and Anaphylactoid Reactions [see WARNINGS AND PRECAUTIONS]
- Bleeding Irregularities[see WARNINGS AND PRECAUTIONS]
- Weight Gain [see WARNINGS AND PRECAUTIONS]
CLINICAL TRIALS EXPERIENCE
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
WARNING: This medication may cause serious bone loss. The risk of bone loss increases with longer use of this medication. This bone loss may be permanent even after you stop using medroxyprogesterone injection. This medication should not be used for longer than 2 years unless other birth control methods will not work for you. The years of adolescence and early adulthood are important for your body to build healthy bones. Use of this medication may increase the risk of broken bones when you are older. Discuss with your doctor the risks and benefits of this medication and other birth control choices.
Keep all your medical/lab appointments. Your doctor may test your bone density while you are using this medication. Be sure to get enough vitamin D and calcium in your diet. Consult your doctor or pharmacist to determine whether you need calcium/vitamin D supplements to help keep your bones healthy.
Use of this medication does not protect you against sexually transmitted diseases (e.g., HIV, hepatitis B, gonorrhea). Consult your doctor or pharmacist if you have any questions.
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Arava (leflunomide)
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LeflunomideInformation 
INDICATIONS
ARAVA is indicated in adults for the treatment of active rheumatoid arthritis (RA):
- to reduce signs and symptoms
- to inhibit structural damage as evidenced by X-ray erosions and joint space narrowing
- to improve physical function
INSTRUCTIONS
Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.
The dose of this medicine will be different for different patients. Follow your doctor’s orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.
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The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.
STORAGE
Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F). Protect from light. Keep out of the reach of children. Do not keep outdated medicine or medicine no longer needed. Store the medicine in a closed container at room temperature, away from heat, moisture.
Keep out of the reach of children. Do not keep outdated medicine or medicine no longer needed. Store the medicine in a closed container at room temperature, away from heat, moisture.
SIDE EFFECTS OF Arava (leflunomide)
In addition to its needed effects, some unwanted effects may be caused by leflunomide. In the event that any of these side effects do occur, they may require medical attention.
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Less common
- Burning feeling in the chest or stomach
- burning, prickling, or tingling sensation in the fingers or toes
- chest pain
- diarrhea
- fast heartbeat
- indigestion
- joint or muscle pain or stiffness
- pounding heartbeat
- severe stomach pain
- shortness of breath
- tenderness in the stomach area
- unusual tiredness or weakness
Incidence not known
- Area rash
- black or tarry stools
- bleeding gums
- blistering, peeling, or loosening of the skin
- bloating
- blood in the stools
- burning, numbness, tingling, or painful sensations
- chills
- clay-colored stools
- confusion
- constipation
- continuing vomiting
- cough or hoarseness
- dark urine
- fainting
- fever with or without chills
- general feeling of tiredness or weakness
- high fever
- large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs
- light-colored stools
- lightheadedness
- lower back or side pain
- pains in the stomach, side, or abdomen, possibly radiating to the back
- pale skin
- pinpoint red spots on the skin
Some of the side effects that can occur with leflunomide may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:
Premarin (Conjugated Estrogens)
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PREMARIN (CONJUGATED ESTROGENS) Information
Premarin is a member of the Conjugated Estrogens group of drugs, based on the female sex hormone estrogen. Estrogen is a hormone essential to the female physiology, on which many of the female-specific body function are based. Among the disorders that may occur when the estrogen quantity becomes insufficient, some examples are: menopause, infertility, and someBreast Cancer types, and ovary function deficiencies, degeneration of the vagina or urethra. The male human body also needs estrogen to function properly, insufficient quantities of this hormone leading to prostate cancer.
Premarin Indications
Premarin is mainly prescribed for the treatment of such disorders as:
- moderate or severe vasomotor symptoms associated with the menopause
- moderate or severe symptoms of vaginal or vulvar atrophy associated with the menopause
- hypoestrogenism due to hypogonadism, castration or primary ovarian failure
- some types of Breast Cancer
- advanced androgen-dependent carcinoma of the prostate
- prevention of postmenopausal osteoporosis – in carefully selected cases.
There are a number of other cases in which Premarin can be prescribed, so if you want to know more about why you have been prescribed this drug, consult your personal health care specialist.
Premarin Warnings
Consult with your personal health care specialist before starting to take Premarin if you are suffering of blood clotting and circulation disorders, abnormal vaginal bleedings, cancer of the breast, uterus or any type of hormone-dependent cancer, as treatment with Premarin might be dangerous in such cases. Also, special care, monitoring or altered dosages may be required for patients that are suffering or have medical history of:
- Uterine fibroids
- Gall bladder diseases
- Diabetes
- Migraines
- Epilepsy
- Asthma
Premarin Dosage
Consult your personal health care specialist to obtain the Premarin dosage best suited to your age and general health condition. Self-medication should never be employed when starting a treatment with this medicine. Never alter the dosage you have been given by your physician, either by modifying the drug quantity or the time interval between intakes.
Premarin Overdose
While it is very unlikely that Premarin overdose will result in fatal consequences, it is recommended that you immediately seek emergency medical care if you suspect you are suffering from an overdose with this drug and / or have unusual symptoms. The most common symptoms of Premarin overdose are nausea, vomiting and vaginal bleeding.
Premarin Missed Dose
You should set up a strict time schedule for your Premarin intakes, to prevent dose omission. However, should you happen to miss a dose, do not take a double dose to make up for the lost one, instead just return to your normal schedule.
Premarin Side Effects
One of the most serious side effects associated with Premarin treatment is the increased risk of developing cancer of the uterus, through development of endometrial hyperplasia. However, this effect can be countered by taking progestins.
Other serious side effects of Premarin use are:
If you are under treatment with any of these drugs, or have recently finished treatment with any of them, please talk with your personal health care specialist as he may decide to alter your Premarin dosage and / or keep you under special monitoring for the duration of the treatment.
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