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FDA approves first oral drug for thalassemia anemia, offering new hope beyond blood transfusions

The US FDA has approved the drug Mitapivat, marketed as Aqvesme, as the very first oral therapy for anemia in adults with alpha or beta thalassemia. This breakthrough offers new hope to patients reliant on frequent blood transfusions for decades. What is thalassemia? Thalassemia is a genetic blood disorder wherein the body cannot make enough…

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Iron Deficiency Medicine: FDA approves first prescription oral medicine to treat iron deficiency in children |

In a groundbreaking development, the FDA has green-lighted Accrufer, an oral iron supplement specially designed for children aged 10 and older struggling with iron deficiency. This innovative treatment provides a hassle-free, non-invasive alternative to traditional supplements. Iron deficiency affects many children and teenagers, often without noticeable symptoms. Tiredness, pale skin, and poor focus are easy…

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FDA approves ‘Jascayd for progressive pulmonary fibrosis: What it means for patients

Exciting news for those affected by progressive pulmonary fibrosis (PPF): The US FDA has granted approval for Jascayd (nerandomilast). This groundbreaking medication goes beyond merely alleviating symptoms, presenting a scientifically validated way to decelerate lung damage. FDA Clears New Lung DrugThe US Food and Drug Administration has approved Jascayd (nerandomilast) tablets for adults with progressive…

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Fluoride Supplement: FDA has restricted this common supplement given to growing children due to major health concern |

FILE – A child shows off her teeth after a dental exam in Concord, N.H., Wednesday, Feb. 21, 2024. (AP Photo/Robert F. Bukaty, file) The U.S. Food and Drug Administration has started efforts to pull ingestible fluoride tablets, lozenges, and drops from the market. These products, often given to children in areas with low fluoride…

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Why FDA recalled over 140,000 bottles of widely used cholesterol pill |

Over 140,000 bottles of Ascend Laboratories’ Atorvastatin Calcium Tablets, a cholesterol medication, have been recalled due to ‘failed dissolution specifications.’ This means the drug may not be absorbed by the body. The recall, classified as Class II, affects various dosages and bottle sizes distributed globally. No illnesses have been reported. Over 140,000 bottles of a…

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Cough Syrup Dangerous Ingredients: FDA and experts warn: Dangerous ingredients to watch out for in a cough syrup |

Cough syrups are a common over-the-counter medication used by millions and people of all ages to relieve symptoms of cold, flu and respiratory infections. While many formulations are safe for use as directed, some cough syrups contain ingredients that pose serious health risks, especially when misused or taken in high doses. Understanding which ingredients to…

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Cough syrup row: Maharashtra bans Coldrif; FDA cites toxic industrial solvent as cause of deaths | Nagpur News

Maharashtra FDA has imposed a statewide ban on Coldrif syrup (Batch No. SR-13) after it was linked to 14 child fatalities in neighboring states due to diethylene glycol contamination NAGPUR: The Maharashtra Food and Drug Administration (FDA) has imposed statewide ban on the sale, distribution, and use of Coldrif syrup (Batch No. SR-13), a paediatric…

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US FDA finds radioactive contamination in spices after shrimp recall |

The US FDA has halted Indonesian spice imports after detecting radioactive cesium 137 in cloves, following earlier massive shrimp recalls. This contamination, a byproduct of nuclear reactions, has raised health concerns despite low levels found. While no contaminated food reached consumers, extensive shrimp recalls are underway. The FDA advises avoiding affected products due to potential…

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