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UK agency pilots biobank to study links between genetics and drug side effects

Pharmaceutical Technology

The biobank will work in parallel with the MHRA’s Yellow Card website, which is used for reporting adverse events and side effects caused by medicines and medical devices, per the 25 May announcement. Side effects due to drugs are responsible for one in every 16 hospital admissions in the UK, based on the announcement.

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Quality of life in patients with chronic health conditions

World of DTC Marketing

According to the CDC, in 2012, 25.5% What happens when someone loses the will to live because they are tired of dealing with chronic health conditions and prescription drugs that have nasty side effects? of US adults had multiple (?2) Our healthcare system is designed to treat health conditions, not patients.

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First FDA pregnancy-approved Pertussis vaccine to protect newborns

European Pharmaceutical Review

Since 2012, the CDC has recommended the vaccine series during the third trimester of each pregnancy. Side effect data related to those given the non-US variation during pregnancy was consistent with data for individuals who were given the non-US formulation post labour.

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Tributes as former NICE, MHRA chair Sir Mike Rawlins dies

pharmaphorum

” Rawlins was knighted in the 1999 Queen’s New Year Honours for services to the improvement of patient protection from the side effects of medicines, and in 2017 was appointed Knight Grand Cross of the Order of the British Empire (GBE) for services to the safety of medicines, healthcare, and innovation.

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How can evidence-based medicine (EBM) methodology support drug withdrawals?

European Pharmaceutical Review

Monitoring and studying the side effects of licensed medicines is an essential part of drug development to ensure public safety. This is usually on a much larger scale than is possible in clinical trials and can uncover less common side effects. Supporting regulators. Study focus. almitrine – a respiratory stimulant.

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Briumvi may struggle to make headway in crowded multiple sclerosis market

Pharmaceutical Technology

As for Briumvi’s side effects, around 45% of patients experienced infections of the upper respiratory tract, which was 4% higher in comparison to Aubagio. As for Briumvi’s side effects, around 45% of patients experienced infections of the upper respiratory tract, which was 4% higher in comparison to Aubagio.

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PM360 2022 Trailblazer Awards Product Launch of the Year Winner GEMTESA

PM360

received FDA approval for once-daily GEMTESA—the first new oral OAB medication approved by the FDA since 2012. With all of this, GEMTESA was shown to be safe and tolerable—with only 2% of study participants discontinuing GEMTESA due to side effects. In December 2020, a startup out of southern California, Urovant Sciences, Inc.,