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Product details Product manufacturer(s) from date of release Date of release Date of statement @ designate as of 12/2012 Rating Date of rating Drug brand/ trademark/ registered date & date of registration Product packaging Label/ image of drug Name, brand or trademark Designation as of 12/2012ritional information Numerating agent Nutritional information Country of origin Country of origin Country of origin Nutritional information U. S. Food and Drug Administration / FDA / European Medicines Agency / US Food and Drug Administration / US Food and Drug Administration / US Food and Drug Administration / World Health Organization / Organization / Office of the national pharmacovigilance information Center for Non-Medicinal Ingredients (CNISIC) Center for Drug Evaluation and Research (CDER and/or IRN) Office of the National Institute of Health (NII) United States of America U. District and/or the Public Health Service Administration U. Food and Drug Administration / FDA / European Medicines Agency / US Food and Drug Administration / US Food and Drug Administration / World Health Organization / Office of the National Pharmacovigilance Information Center Center for Non-Medicamental Drugs (CPCC) Cipla Pharmaceuticals Corporation d/m nt company NII United States of America U. Food and Drug Administration / FDA / Office of the National Pharmacovigilance Information Center Center for Drug Evaluation and Research (NII) United States Food and Drug Administration / FDA / Office of the General Pharmaceutical Research and Markets Committee (GPhC) U. Department of Health and Human Services Agency for the Health Sciences andamp; Administration of Health Insurance Portability Data FDA / United States Food and Drug Administration / United States Department of Health and Human Services Agency for the Health Sciences andHealth Human Services Agency Agency Agency Agency Office of Pharmaceutical Research and Markets and Agency Office of National Library of Medicine Health and Human Services Agency Office of the Science and Technology Information Center Health and Human Services Office of the Science and Technology Information CenterProduct details Description Samantha M, et al. (2015) The management of endometriosis: a global perspective. Int J Endo Investig. 5, 1. 1 Saleetto E, Bhatt JY, et al. International Journal of Obstetrics and Gynecology, 21, 9.The Depo Provera injection is injected into your uterus, and it has the same active ingredient. Depo Provera is the generic name of the hormone called medroxyprogesterone acetate. It’s produced by the Depo drugmaker and is used for the treatment of and certain types of meningioma.
The medication is injected slowly into your body, typically one-half to one-half-th follicles, and the injection is repeated every three months.
Depo Provera is available without a prescription, as a generic. However, some medical providers may offer it as a subcutaneous injection. It’s also available by prescription, as a subcutaneous injection. And the FDA has approved Depo-subcutaneous injections for men with the following conditions:
Depo Provera is also available for injection only, but it’s also prescribed for certain medical conditions, including:
Because Depo Provera is a reversible form of birth control, a medical provider may recommend a subcutaneous, injectable form of Depo-subcutaneous Depo-provera if the medical provider determines the type and severity of the condition is appropriate.
For a complete list of Depo Provera subcutaneous injections, see the “Are you sure you should not use this medication?” section below.
Depo-subcutaneous injections:
The FDA has approved Depo-subcutaneous injections for all of these conditions:
Because Depo-subcutaneous injections are used only for a limited period of time, a medical provider may recommend a subcutaneous injection over an oral contraceptive injection.
This is not recommended for a variety of reasons, such as:
Depo Provera is available as an injectable solution. And the FDA has approved it for all of these conditions, including:
Depo-subcutaneous Depo-provera is a subcutaneous injection, as opposed to the oral contraceptive method, which is the method that’s available through the Depo birth control manufacturer. Depo-subcutaneous Depo-provera is injected slowly into the skin using a dosing syringe, and it lasts for three months. Depo-subcutaneous Depo-provera injections are injected once every three months.
Depo-SubQ Provera 104 needs to be given by subcutaneous (hypodermic) injection once every 12 weeks. This is not an intramuscular injection and must be given by someone trained and knowledgeable on how to give a subcutaneous injection.
The main active ingredient in Depo-SubQ Provera 104 is Medroxyprogesterone acetate 104 mg.
The risks are low, but some women experience side effects when using Depo-SubQ Provera 104. Minor ones include (spotting) or some gain weight. Positive side effects are also a possibility, too — lighter bleeds are fairly common.
The chances of serious side effects from birth control pills are extremely unlikely, but some cases have been documented, such as unexplained vaginal bleeding, severe pelvic pain, severe abdominal pain, and bone pain. Depo-SubQ 104 has been associated with lower bone mineral density (BMD). However, pregnancy results in a greater potential loss of BMD. This method is not recommended for younger patients who have not yet reached their peak bone mass or patients with osteoporosis. Alternatives to Depo-SubQ Provera would be the pill, patch, ring.
If you experience swelling/itching of your face/throat/tongue, trouble breathing, or severe dizziness, this may indicate an allergic reaction, please call 911 or get to the emergency room to receive appropriate emergency medical treatment.
Do NOT take this medication if:
• No female who has been diagnosed with a confirmedational arterial thrombosis or pulmonary embolism has been observed to have an increased risk of a stroke or a heart attack if administered in the last 3 months. • No female who has been diagnosed with arterial disease or pulmonary embolism has been observed to have an increased risk of developing a cerebrovascular event during minoxidil treatment. • No brain tumor or cerebral arterial thrombosis has been reported with this medication. If a woman history of stroke or deep vein thrombosis or if she is pregnant or planning to become pregnant is advised to stop the medication, she should consult a doctor before taking this drug.Before starting treatment with Depo-SubQ Provera, tell your doctor if:
• You have unexplained vaginal bleeding, vein thrombosis, pulmonary embolism, or a history of stroke or heart attack. • You have polycystic ovary syndrome or underactive thyroid. • You have ever had an allergic reaction to this drug. Most people who have this medication do not have any adverse effects.Before starting treatment with Depo-SubQ Provera, inform your doctor about any medical conditions you have, including liver or kidney disease, adrenal gland disease, adrenal gland disease of unknown etiology, or history of stroke or heart attack. This includes any history of stroke or heart attack.
Depo-SubQ 104 can cause side effects, so be sure to tell your doctor about all the drugs you are taking. Also, let your doctor know if you are urinating, how many tablets (how often you use this drug) will help the the most, and how often you should have sex. This will let them know if you are takingmology.
This is a recurrence prevention mechanism. When you do get a recurrence, stop taking the drug and get medical help right away, even if there are no side effects.
Before starting treatment with Depo-SubQ Provera, tell your doctor about all the medicines you are taking, including any prescription and nonprescription medicines, vitamins, and herbal supplements.
Get medical help or call your doctor at the nearest hospital if you have side effects, so that you can get the right treatment for your condition.
The risk of pregnancy is extremely unlikely, but the procedure are possible if you have been approved on the date of your pregnancy.
Depo-Provera can cause Depression in many people with the symptoms of depression. This is usually mild to moderate. It is often used to treat depression because it has the same effects as the contraceptive methods.
Depo-Provera can also cause other types of side effects such as:
Depo-Provera can also cause some serious side effects, particularly:
If you are experiencing any of these side effects, talk with your doctor or health care professional.
If these side effects do not go away, or if they bother you, talk with your doctor or pharmacist.
Depo-Provera does not cause depression in everyone with the following conditions:
Some of the most common side effects of Depo-Provera include:
If you are experiencing any of the above side effects, talk with your doctor or health care professional.
If you are experiencing these side effects, talk with your doctor or pharmacist.
There is some evidence that Depo-Provera is effective in treating some types of depression. However, there are not many studies comparing Depo-Provera to other medications. This is because there are not many other types of hormonal contraceptives that are used to treat depression.
Depo-Provera and other contraceptives are not recommended for long term use due to their low efficacy. It is best to talk with your doctor if you are pregnant or plan to become pregnant.
In addition, there are many types of hormonal contraception and hormonal contraception options available. However, there are also other types of hormonal birth control that can be used to prevent pregnancy.
Depo-Provera is used to prevent pregnancy by preventing ovulation and thickening the cervical mucus to prevent sperm from reaching the egg. Depo-Provera does not cause a pregnancy.
Yes, Depo-Provera is generally safe. However, there are some risk factors that may increase the risk of getting pregnant while taking this medication.
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