Photo: NEY
Big Pharma strikes again.
ADHD ADVERSE EVENTS
Australia’s pharmaceuticals watchdog is investigating a spike in adverse event reports for Vyvanse, the country’s most commonly prescribed ADHD medication.
The increase coincides with a leap in prescriptions for ADHD, as well as a growing focus on the effectiveness of treatments like Vyvanse on social media.
There were 320 adverse event reports relating to Vyvanse — or lisdexamfetamine dimesilate — to the Database of Adverse Event Notifications (DAEN) in the first six months of the year.
This is compared to just nine reports in the six months before.
The most common adverse events reported were ineffectiveness, anxiety, product labelling issues, therapeutic response decreases, and insomnia.
The World Health Organization’s equivalent database for reporting adverse medicine events has also seen an uptick in reports relating to the active ingredient of Vyvanse, lisdexamfetamine.
The TGA said its investigations included ongoing independent testing of Vyvanse through TGA laboratories, and that it did not comment on open investigations.
“This investigation is the result of a recent increase in adverse event notifications relating to concerns about quality, safety, and reduced effectiveness,” a spokesperson said.
“Any regulatory actions that arise will be communicated.”
The TGA also confirmed it had seen an increase in adverse events relating to ADHD-prescribed stimulants more generally, with 754 events registered for the most common drugs — methylphenidate, dexamphetamine and lisdexamfetamine — between January 2015 and June 2025.
Vyvanse was the only one significant enough to constitute a ‘safety signal’, which is triggered when information suggests a possible causal relationship between adverse events and a drug.
According to a Royal Australian and New Zealand College of Psychiatrists (RANZCP) spokesperson, stimulants, like Vyvanse and Ritalin, “appear to normalise some of the brain’s main neurotransmitter systems, allowing better regulation of parts of the brain involved in executive function, particularly the frontal lobe”.
Although, as was discovered earlier this year, despite medication helping with the direct effects of ADHD in the short-term, scientists also found the drugs did not improve their overall quality of life.
Furthermore, there wasn’t enough evidence to draw conclusions about the effects of treatments in the long-term.
ADHD medications do not improve quality of life, study finds
Vyvanse prescriptions almost doubled from 958,831 in 2022 to more than 1.78 million in 2024, according to the Pharmaceutical Benefits Scheme (PBS).
When are people going to learn that Big Pharma is not your friend.
Their whole purpose is to make you a consumer, not to fix your ailments.
BIG P-HARMA
Modern medicine has made humanity sicker and weaker than ever, all by design.
Hospital and doctors are largely snake oil salesmen, and the ‘science’ underpinning most of the practices and ideologies of this industry is fraudulent.
Here on the website, from ultrasounds to shingles, Alzheimer’s, organ donation, comas, birth trauma and more, we have covered the dark sides of the medical industry.
The medical fraudsters are constantly being exposed as their lies collapse under their own weight.
Let’s take a look at some of the most recent revelations to emerge:
Speaking of pill popping, how about in 2022 when a breakthrough study was published in Molecular Psychiatry that conclusively debunked the theory that depression can be cured with antidepressants.
And when is say debunked, I mean debunked.
According to the study, there is no clear evidence that depression is caused by low serotonin levels. Headlines spread throughout the scientific community who could not refute the comprehensive research.
Who could forget when Big Pharma destroyed the lives of countless millions with their opioid epidemic, fuelled in part by the same FDA and regulatory bodies that fuelled the COVID ‘pandemic’.
Opioid Crisis: How FDA Regulation Failures Allowed it to Happen
They lie, and people die, or become lifelong customers to the same industry that mangled them.
Driven by profit and power, Big Pharma has shown no regard for personal safety or legal regulations, as consumers continue to trust companies caught intentionally lying to the public, promoting products underpinned by non-objective science and deception.
In the medical industry, there is little room for independent thinking.
Blind faith arises out of fear of taking responsibility, from feelings of inadequacy in the face of ‘expertise’, or reluctance to question or offend the ‘experts’ in their related field.
Unquestioning faith is all-pervasive in the patient-doctor and patient-pharma relationship, to the detriment of patients all across Australia and the world.
Many people just follow the ‘expert advice’ of their doctor to get things checked out, only to find themselves getting worse off from the very moment they paid a visit.
It is no wonder this industry is one of the most least respected in the world, even before the ‘pandemic’.
The entire medical industry has quite a lot to answer for, and if you would like to learn more about the influence of Big Pharma right here in Australia, make sure to check out this old classic TOTT gem if you haven’t already:
Stay away from the drug dealers, folks!
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DOES NO
TGA tests drugs prior to AU release? NOT!
Expecting ANY Non Biased – Actually, ANY ‘Result’, after the ‘Mythical Beastie’ CONVID Something, & After, apparently ‘CONvid’ DIDN’T rate a ‘Proper Investigation’@the Get Go – So Good luck on anything coming from the Corporate ‘Guards’ = The TGA & Agency/Associated Confederates!
Standard Ops@TGA investiGateIon; Company – Apologies. Govt agency REP(1) evaluates pHARMa products presented to market. Without even checking the complete SDS(2)>(Probably aren’t capable these days anyway), the REP reaches into his top drawer, & pulls out a Big green tick of Approval – With ‘Enough quotas’- a magical free trip to a pHARMa resort Not near You! Or, enough Toiling – Maybe even a Revolving door experience. As with other NotMyGov.Con ‘Agencies’ & NOT Watchdogs, Including the catchy – IN association with ‘Private Partnerships’ Deals, Do ANY of them have ANY Cred anymore? – Rhetorical.
(1) REP; Representatives Expanding Pharma.
(2) SDS; product Safety Data Sheets; Original SDS for SARS COV something Jabs(Both Moderna & Pfizer[one Doesn’t wonder About Pfizer’s BNT162b2 Jabs, which the ‘Header’ should have had the TGA in a quandry, Per ‘ATTACHMENT A’; WARNING; THIS VACCINE MAY CAUSE SERIOUS ILLNESS AND DEATH. {Company’s Own Capitals – Obviously ‘Death & Serious Illness’ as a ‘Health Concern – DIDN’T concern the TGA – OR other Medics!!}]), had that much Actual missing data, one could have used it as Slab mesh – STILL O.K’d by TGA (EUA or Not). This along with Moderna’s ‘Patented’ Cov sequence Inputs in 2016 – Which magically appeared 3 Years later in ‘CONVID-19’. Along with other Embarrassments such as the 2015 Rothschilds registrations of Year 2019 Cov AppaRent disease kits (RT-PCR LAB only test [Shipped Globally 2017/18 – Including OZtopia]). And On, And On. Did I mention ‘CredibiliTie’ (Credibility – Either).
Truth; Conspiracy Theory + 6 Months – What we need are Stricter rules on Bull shit & MIS/DISinfo = That’s the main Purveyors out of Work = NotMyGov & Media.
Wellness, unity.
After what we have witnessed during Convid1984, I wouldn’t trust the TGA to investigate any of Harma’s toxic products. Over 90% of its funding is provided by Harma.