The 1970s was a decade of significant medical advancements. However, some medications from that era have since been pulled from the market due to safety concerns. Here’s a look at 20 o… Read More
SIMLANDI is the first citrate-free, high-concentration biosimilar to be designated interchangeable to Humira in the U.S.
SIMLANDI is the first biosimilar approval under the strategic part… Read More
New Delhi: The drug major Akum Pharmaceutical has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to manufacture… Read More
In the dynamic landscape of oncology therapeutics, understanding the trends and performances of leading drugs is crucial for stakeholders across the healthcare and life sciences sectors. The… Read More
The US Food and Drug Administration (FDA) has issued letters to several companies to include a class-wide boxed warning about the risk of T-cell malignancies on their CAR T-cell therapies… Read More
Presented by Idorsia Pharmaceuticals: Delivered every Tuesday and Friday by 12 p.m., Prescription Pulse examines the latest pharmaceutical news and policy… Read More
GLP-1 receptor agonists likely don’t cause suicidal thoughts or actions, according to a preliminary evaluation by the FDA.
The investigation was prompted after the FDA Adverse Event… Read More
The US Food and Drug Administration is investigating allegations of adverse drug reactions, including hair loss and suicidal thoughts, in patients using Wegovy, Mounjaro, and Ozempic.
GLP-1… Read More
Safety risks found in a postmarketing trial with the Janus-associated kinase (JAK) inhibitor tofacitinib (Xeljanz) appear to have influenced prescribing patterns across the class for rheum… Read More
Presented by Arnold Ventures: Delivered every Tuesday and Friday by 12 p.m., Prescription Pulse examines the latest pharmaceutical news and policy. Nov… Read More
Headlines in type 2 diabetes this year featured new approvals, continued access issues for GLP-1 agonists, guidance on surgery timing with that widely used class of drugs, and emerging ris… Read More
The FDA added the postmarketing reports of ileus, or blocked intestines, to the drug labeling for semaglutide (Ozempic).
“Because these reactions are reported voluntarily from a popu… Read More
Is Toradol a Narcotic?
Toradol, known by its generic name ketorolac, is a non-steroidal anti-inflammatory drug (NSAID) used to manage pain and inflammation in various medical conditions… Read More
The tide may be turning on respiratory syncytial virus (RSV), a seasonal scourge that’s responsible for a substantial number of hospitalizations and deaths among older people and you… Read More
The History of Botulinum Toxin
The history of Botulinum Toxin, often referred to as “botox”, is a fascinating journey that spans over several decades. This potent neurotoxin… Read More
The FDA is recommending that healthcare providers, laboratory personnel, and facilities consider alternative products amid the recall of the Quidel Triage Cardiac Panel.
The AROMI trial ha… Read More
Thyroid cancer concerns are out these days, and we also have to address them. Check out the latest reports below.
Thyroid cancer concerns
The European Medicines Agency (EMA) has issued a dru… Read More
Lecanemab (Leqembi) showed clinical benefit in early Alzheimer’s disease in its confirmatory trial, paving the way for traditional approval of the drug, an FDA advisory committee sai… Read More
An FDA advisory committee voted 6-2, with one absention, that a novel, synthetic knee meniscus replacement’s benefits do not outweigh its risks, and thus is not suitable for marketin… Read More
The aim of real-world evidence, or RWE, is to improve healthcare decision-making by complementing data generated from randomized controlled trials (RCTs). While RCTs come in handy to investi… Read More
Confidential Pfizer Documents reveal Covid-19 Vaccination is going to lead to Depopulation
BY THE EXPOSÉ ON MARCH 8, 2023
Covid-19 vaccination is going to lead to mass… Read More
On Monday, medical device company HistoSonics announced that the US Food and Drug Administration (FDA) has approved the company’s sponsored #HOPE4KIDNEY investigational device exemptio… Read More
January 5, 2023
Media contact: National Consumers League – Katie Brown, [email protected], 202-823-8442
Washington, D.C. – The Food and Drug Administration (FDA)’s decision… Read More
Bharat Book Bureau Provides the Trending Market Research Report on “Real-world Data (RWD) by Source (EMR, Claims, Pharmacy, Disease Registries), Application [Market Access, Drug Develo… Read More
Hairolays an important role in determining a person’s self-image, social perceptions, and psychosocial functioning. The problem of hair loss is psychologically damaging and causes inte… Read More
The .gov means it’s official.Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.The site i… Read More
Today we live in a world where medical technology and devices have become more advanced than ever before. Here is a list of the top 10 medical technologies in 2022
Emerging technologies ha… Read More
On July 23rd, 2022, Singapore HSA announced the launch of a voluntary notification initiative for companies that deal with health supplements and traditional medicines. The aim is to establi… Read More
The US Food and Drug Administration (FDA) has issued a warning for Secura Bio’s Copiktra (duvelisib) after a clinical trial found the drug was associated with a higher risk of serious… Read More
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The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee). Image for illustration purposesMega Doctor News
Today (… Read More
– Results of bempedoic acid, ezetimibe and atorvastatin triple therapy study published in March issue of Atherosclerosis –
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