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    Along with its needed effects, furosemide (the active ingredient contained in Lasix) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Lasix (furosemide)." sanofi-aventis , Bridgewater, NJ. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Check with your doctor immediately if any of the following side effects occur while taking furosemide: Some side effects of furosemide may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them: Applies to furosemide: compounding powder, injectable solution, intravenous solution, oral liquid, oral solution, oral tablet Common (1% to 10%): Hyponatremia, hypochloremia, hypokalemia, blood cholesterol increased, blood uric acid increased, gout Uncommon (0.1% to 1%): Thirst, glucose tolerance decreased Rare (0.01% to 0.1%): Anorexia, serum triglycerides increased Frequency not reported: Hyperglycemia, diabetes mellitus, hyperuricemia, metabolic alkalosis, hypocalcemia, hypomagnesemia, hypovolemia, dehydration, tetany, serum potassium decreased, Pseudo-Bartter syndrome, electrolyte disturbances, serum calcium decreased Common (1% to 10%): Hemoconcentration Uncommon (0.1% to 1%): Thrombocytopenia Rare (0.01% to 0.1%): Eosinophilia, leukopenia, bone marrow depression Very rare (less than 0.01%): Hemolytic anemia, aplastic anemia, agranulocytosis Frequency not reported: Anemia, thrombophilia Uncommon (0.1% to 1%): Pruritus, bullous exanthema, rash, urticaria, purpura, erythema multiforme, exfoliative dermatitis, photosensitivity Rare (less than 0.1%): Lyell's syndrome and Stevens-Johnson syndrome, acute generalized exanthematous pustulosis, drug rash with eosinophilia and systemic symptoms Frequency not reported: Toxic epidermal necrolysis, bullous pemphigoid, sweating Uncommon (0.1% to 1%): Dry mouth, nausea, bowel motility disturbances, vomiting, diarrhea, constipation Rare (less than 0.1%): Gastric distress, acute pancreatitis Frequency not reported: Pancreatitis, oral and gastric irritation, cramping Uncommon (0.1% to 1%): Blood creatinine increased, urea increased Rare (less than 0.1%): Interstitial nephritis, acute renal failure Frequency not reported: Nephrocalcinosis in premature infants, nephrolithiasis in premature infants, GFR decreased, tubulointerstitial nephritis Uncommon (0.1% to 1%): Deafness, fatigue Rare (less than 0.1%): Sensation of pressure in the head, dysacusis, asthenia, fever, febrile conditions, malaise Frequency not reported: Weakness, sudden death, hearing disorders, hearing loss, paradoxical swelling Uncommon (0.1% to 1%): Cardiac arrhythmia Rare (less than 0.1%): Vasculitis Frequency not reported: Systemic vasculitis, necrotizing angiitis, orthostatic hypotension, thrombophlebitis, acute hypotension, circulatory collapse, persistent patent ductus arteriosus during the first few weeks of life in premature infants with respiratory distress syndrome, blood pressure decreased, shock, hypotension, thrombosis, orthostatic blood pressure decreased Rare (0.01% to 0.1%): Paresthesia, vertigo, dizziness, sleepiness, tinnitus, hyperosmolar coma Frequency not reported: Hepatic encephalopathy, headache, fainting and loss of consciousness, drowsiness, lethargy, sweet taste1. Lasix Side Effects in Detail - zoloft 200 mg side effects Common Side Effects of Lasix Furosemide Drug Center - RxList Cardiomyopathy In Your Cat- When Your Pet's Heart Fails
     
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    The mother of a Mentor woman describes alarming changes in her daughter after being prescribed a popular antibiotic that she suspects played a role in her daughter's death.47-year-old Deana Poghen was struck and killed on I-90 in Mentor last Christmas Eve. Food and Drug Administration issued new warnings and label changes for drugs like Cipro that belong to a family of antibiotics known as fluoroquinolones."Serious side effects," warned the FDA, "outweigh the benefits for many patients.""Treatment should be stopped immediately if side effects are reported."But the FDA warning came too late for Poghen who believed the drug was safe. Florence Summers suspects Cipro, one of the nation's most widely used antibiotics, caused serious side effects that contributed to her death."She was beautiful, she was vibrant and happy," said Summers, "she loved life--and lit up a room when she came in."But our exclusive investigation found that within months--it all began to unravel."If she would take a shower, her skin would hurt," said Summers, "she lost the sensation of warmth and cold."Poghen's mother says her daughter took the drug for only a few days four months earlier but immediately serious side effects began to surface."After the very first dose," said Summers, " she had a severe reaction"Summers said her daughters "skin began crawling" and she would beg her to "keep her safe."The family said it did everything they could--but nothing helped and the "bad thoughts" continued. One of the nation's leading drug safety advocates says Poghen is not an isolated case and the FDA has found at least 600 suicide related cases reported in the last 18 years--133 deaths. Charles Bennett says "even as few as one or two doses--they can develop serious, permanent and disabling psychiatric toxicity.""These are things like being unable to work, unable to concentrate, body pain, and very, very disabling."Bennett also remains concerned that new warning labels do not go far enough."The medication guides in the July 26, 2016 updated fluoroquinolone labels do not include the Boxed Warnings stating that the fluoroquinolone antibiotics may result in disabling and potentially irreversible serious adverse reactions."Bennett also says drug companies have not sent health care professionals letters informing them of serious changes contained in new labels. The FDA, responding to our requests, says health professionals are "advised to counsel patients regarding disabling and potentially irreversible serious adverse reactions" may occur. In medication guides for patients, the FDA says it also warns that "some of these serious side effects can happen at the same time and could result in death."Read the entire FDA statement here: Prescribing Information is intended for the health care professional, and the Medication Guide is intended for the patient. In the Prescribing Information (Section 17), the health care professional is advised to counsel patients regarding disabling and potentially irreversible serious adverse reactions that may occur. The Medication Guide is written at the 6th to 8th grade level using simplified wording that is consistent with the Prescribing Information. Under the beginning section of the Medication Guide entitled, “What is the most important information I should know about DRUG? Ciprofloxacin - Wikipedia clonidine mg Label - FDA Fluoroquinolone Antibiotics - Cipro Lawsuit - Levaquin Lawsuit
     
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