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The most common side effect of valsartan is dizziness. This can occur as the body adjusts to the medication, particularly when standing up quickly.

Valsartan itself has not been discontinued as a medication. However, certain batches of valsartan were recalled due to contamination with impurities, such as N-nitrosodimethylamine (NDMA), which is a potential carcinogen. This led to recalls by some manufacturers to ensure patient safety. Patients taking valsartan should consult their healthcare provider to determine if their medication is affected and discuss alternative treatment options if necessary.

Valsartan is an effective medication for managing high blood pressure. It belongs to a class of drugs known as angiotensin II receptor blockers (ARBs), which help relax blood vessels and improve blood flow. This can lead to lower blood pressure and reduce the risk of complications such as heart attack and stroke. However, the suitability of valsartan for an individual should be determined by a healthcare provider, considering the patient's specific health needs and medical history.

Valsartan products have been subject to recalls in the past due to the presence of impurities such as N-nitrosodimethylamine (NDMA) and N-nitrosodiethylamine (NDEA), which are classified as probable human carcinogens. The specific batches and manufacturers involved in recalls can vary. It is important for individuals to check with the FDA or their healthcare provider for the most current information regarding specific recalls.

Valsartan, like any medication, can have potential disadvantages or side effects. Some common side effects include dizziness, headache, and fatigue. More serious but less common side effects may include kidney problems, high potassium levels, and allergic reactions. It is important for patients to discuss their medical history and any concerns with their healthcare provider to determine if valsartan is appropriate for them.