Check with your doctor immediately if any of the following side effects occur: Incidence not known. The discontinuation rate due to bleeding events was approximately 1% in the ELIQUIS-treated patients compared to 0.4% in those patients in the placebo group in the AMPLIFY-EXT study.Bleeding results from the AMPLIFY-EXT study are summarized in Table 7.Adverse reactions occurring in ≥1% of patients in the AMPLIFY-EXT study are listed in Table 8.Less common adverse reactions in ELIQUIS-treated patients in the AMPLIFY or AMPLIFY-EXT studies occurring at a frequency of ≥0.1% to <1%:© Eliquis Patient Information is supplied by Cerner Multum, Inc. and Eliquis Consumer information is supplied by First Databank, Inc., used under license and subject to their respective copyrights.Copyright © 2020 by RxList Inc. RxList does not provide medical advice, diagnosis or treatment. We compare the side effects and drug effectiveness of Microzide and Chlorthalidone. Other side effects of Eliquis include: skin rash, allergic reactions, fainting, nausea, and; anemia. Along with its needed effects, a medicine may cause some unwanted effects. Patients may have a higher risk of bleeding if Eliquis is taken alongside other medicines that increase the risk of bleeding, such as aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), warfarin (Coumadin), There are no adequate and well-controlled studies of Eliquis in pregnant women. While these side effects can be uncomfortable as well as inconvenient, in many cases their severity lessens as your body becomes used to taking Microzide. Side Effects & Adverse Reactions. The study is created by eHealthMe based on reports (from sources including the FDA) of 260,936 people who take Valsartan and Microzide, and is updated regularly. This answer was If you are taking an aminoglycoside, loop diuretics can lead to side effects and should be avoided. The most common side effects of Eliquis are related to bleeding. Experiencing light bleeding, often called spotting, after taking the morning-after pill is pretty normal. You may report side effects to FDA at 1-800-FDA-1088.The following serious adverse reactions are discussed in greater detail in other sections of the prescribing information.Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials 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.The safety of ELIQUIS was evaluated in the ARISTOTLE and AVERROES studies [see The most common reason for treatment discontinuation in both studies was for bleeding-related adverse reactions; in ARISTOTLE this occurred in 1.7% and 2.5% of patients treated with ELIQUIS and warfarin, respectively, and in AVERROES, in 1.5% and 1.3% on ELIQUIS and aspirin, respectively.Tables 1 and 2 show the number of patients experiencing major bleeding during the treatment period and the bleeding rate (percentage of subjects with at least one bleeding event per 100 patient-years) in ARISTOTLE and AVERROES.In ARISTOTLE, the results for major bleeding were generally consistent across most major

Acute Myopia and Secondary Angle-Closure Glaucoma: Hydrochlorothiazide, a sulfonamide, can cause an idiosyncratic reaction, resulting in acute transient myopia and acute angle-closure glaucoma. As always, you should consult with your healthcare provider about your specific health needs. Adverse reactions related to bleeding occurred in 219 (13.3%) ELIQUIS-treated patients compared to 72 (8.7%) placebo-treated patients. Important: This content reflects information from various individuals and organizations and may offer alternative or opposing points of view.

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