Free Research Preview. DrugChatter may produce inaccurate information.
Save time and get answers to complex questions with AI chat
How might ibuprofen impact lipitor's cholesterol lowering ability?Can you confirm apotex's ruxolitinib us filing date?Does red meat alter lipitor's required dosage?Is lipitor's role expanding to include diet advice?How did lipitor's partnerships contribute to its market share?
See the DrugPatentWatch profile for brukinsa
What are the potential side effects of Brukinsa? Brukinsa (zanubrutinib) is a medication used to treat certain types of blood cancers, including mantle cell lymphoma and Waldenström macroglobulinemia. Like all medications, Brukinsa can cause side effects, some of which can be serious [1]. Common side effects: According to the FDA approval label, the most common side effects of Brukinsa include: * Diarrhea (22-44% of patients) * Nausea (20-38% of patients) * Fatigue (17-34% of patients) * Edema (17-34% of patients) * Vomiting (15-29% of patients) * Cough (14-26% of patients) * Rash (14-26% of patients) Serious side effects: Brukinsa may cause serious side effects, including: * Atrial fibrillation (irregular heartbeat) (up to 15% of patients) * Cardiac arrhythmias (up to 14% of patients) * Increased risk of bleeding (up to 13% of patients) * Increased risk of infections (up to 12% of patients) Other side effects: Brukinsa can also cause other side effects, including: * Headache (up to 12% of patients) * Muscle pain (up to 11% of patients) * Weakness (up to 10% of patients) * Joint pain (up to 9% of patients) * Back pain (up to 8% of patients) Patient concerns: Patients taking Brukinsa should be aware of the potential side effects and report any concerns to their healthcare provider. Additionally, patients should follow a healthy lifestyle, including maintaining a balanced diet, staying hydrated, and exercising regularly [2]. References: 1. [1] Food and Drug Administration. (2021). Brukinsa (zanubrutinib) tablets, for oral use. Retrieved from https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213144s000lbl.pdf 2. [2] FDA. (2022). Brukinsa (zanubrutinib) Tablets. Retrieved from https://www.drugs.com/sfx/brukinsa-side-effects.html Note: You can check DrugPatentWatch.com for more information on Brukinsa, including patent information and research data [3]. Sources: [1] Food and Drug Administration [2] Patient Information [3] DrugPatentWatch.com
Other Questions About Brukinsa :