Penicillin Penny

Do antibiotics raise risk of juvenile arthritis?

People aren't petri dishes: Why antibiotics fail

Antibiotics can goad 'superbugs' into ganging up on us

Scientists watch as bacteria evolve antibiotic résistance

Common Herbicides Appear to Cause Antibiotic Resistance

Unnecessary and/or inappropriate antibiotics
prescriptions are estimated at 45 million per year.

Ivermectin, 'Wonder drug' from Japan

Ivermectin inhibits SARS-CoV-2 in vitro

Chloroquine: potent inhibitor of SARS infection

Key to Defeating COVID-19 Already Exists

AbCellera/Eli Lilly Co-Develop COVID-19 Therapeutic Antibodies

Antibiotics that kill gut bacteria also stop growth of new brain cells

Antimicrobial Activity of Cannabinoids

Current antibiotic drugs have limited efficacy against multidrug resistance bacteria and their usage can be limited due to their toxicity for prolonged treatments; therefore, the discovery of an antimicrobial therapy of plant origin will no doubt be a great advancement in the field of anti-infectives.
Several cannabinoids have been found to have potent antimicrobial activity against Gram-positive pathogens such as MRSA isolates.

Endocannabinoids have also been shown to be effective in eradicating biofilms.

Combination therapy with bactericidal agents that possess different modes of action such as polymyxin B have shown synergism and broad-spectrum activity.

There is evidence other compounds found in C. sativa such as terpenes have promising antimicrobial activity, warranting further investigation.

As bacteria are rapidly developing resistance against existing drugs, cannabinoids present a potential new source of antibiotics.

Antiviral potencies of cannabinoids against SARS-CoV-2

Binding of Δ9-THCA, Δ9-THC, CBN, CBD, and CBDA with binding active site of SARS-CoV-2 Mpro had good docking scores compared to reference compound a-ketoamide with similar binding pocket of SARS-CoV-2 Mpro.

Δ9-THC and CBD showed a slightly higher HOMO-LUMO energy gap in DFT calculations; these molecules are stable with SARS-CoV-2 Mpro.

In MD simulations, Δ9-THC- or CBD-SARS-CoV-2 Mpro complexes showed better conformation stability than Δ9-THCA, CBN, and CBDA complexes.

Δ9-THC or CBD bind to SARS-CoV-2 Mpro with stable conformations.

Based on privileged safety index CBD and Δ9THC in human and their current in vitro potencies against SARS-CoV-2, it can be concluded that these compounds are potential antiviral molecules towards SARS-CoV-2 and may have worked as dual-acting against SARS-CoV-2, not only block the viral translation procedure by inhibiting SARS-CoV-2 Mpro but also reduce pro-inflammatory cytokines levels in lung cells by acting as agonists of CB2 receptor.

Secret war against counterfeit science

"Bacteria have developed résistance to antibiotics with an alacrity far exceeding any expectation - and challenging, indeed, widespread scientific assumptions about the mechanisms of bacterial evolution.

The response to declining effectiveness of antibiotics is - more antibiotics!

If technology caused a temporary decline in well-being, the answer is more powerful antibiotics delivered in more potent ways." - Charles Eisenstein

1820 Eleven doctors set up the US Pharmacopeia and record the first list of standard drugs.

1911 US v. Johnson, the Supreme Court rules that the 1906 Food and Drugs Act does not outlaw false medical claims but only false and misleading statements about the ingredients or identity of a drug.

1912 Congress passes the Sherley Amendment to overcome the ruling in US v. Johnson.

The Act outlaws labeling medicines with fake medical claims that is meant to trick the buyer.

1937 Elixir Sulfanilamide, contains the poisonous liquid, diethylene glycol, killing 107 persons, many of whom are children.

1938 Congress passes the Federal Food, Drug, and Cosmetic Act (FDC), which requires that new drugs show safety before selling.

1941 Nearly 300 deaths and injuries result from the use of sulfathiazole tablets, an antibiotic, tainted with the sedative, phenobarbital.

1950 Alberty Food Products Co. v. US, a US Court of Appeals rules that the directions for use on a drug label must include reason for use.

1951 Congress passes the Durham-Humphrey Amendment, which defines the kinds of drugs that cannot be used safely without medical supervision.

The amendment limits sale of these drugs to prescription only by a medical professional.

All other drugs are to be available without a prescription.

1952 Nationwide investigation by FDA reveals that chloramphenicol, an antibiotic, caused nearly 180 cases of often deadly blood diseases.

1953 Factory Inspection Amendment clarifies previous law and requires FDA to give manufacturers written reports of conditions seen during inspections and results of factory samples.

mauled by bayer cipro


Musculoskeletal Complications of Fluoroquinolones

Fluoroquinolones Are Too Risky for Common Infections

Ciprofloxacin inhibition of experimental fracture healing

"Fluoroquinolone antibiotics are commonly used to treat a variety of infections, including urinary tract, respiratory tract, gastrointestinal tract, skin, bone, and joint infections.

First introduced in the 1980s to treat gram-negative bacterial infections, the popularity of fluoroquinolone antibiotics has increased because of their broad antimicrobial spectrum, multiple approved indications, and favorable pharmacokinetics.

In fact, between 1995 and 2002, fluoroquinolone prescribing tripled, making fluoroquinolones the class of antibiotics most commonly prescribed to adults in the United States.

Despite their popularity, a number of adverse reactions have been attributed to fluoroquinolones, including adverse reactions on musculoskeletal tissues.

Fluoroquinolone-associated tendinopathy, which was first reported in the literature in 1983, is a widely recognized complication of fluoroquinolone use that eventually led the U.S. Food and Drug Administration to add a black box warning label to all fluoroquinolones in 2008, citing increased risk of tendinitis and tendon rupture.

Fluoroquinolones exert a toxic effect not only on tendons but also on cartilage, bone, and muscle.

Knowledge of the full spectrum of the negative effects of fluoroquinolone antibiotics on the musculoskeletal system is currently evolving, and much of the mechanistic nature of the toxicity has not yet been fully elucidated." - Musculoskeletal Complications of Fluoroquinolones: Guidelines and Precautions for Usage in the Athletic Population, Mederic M. Hall, MD, Jonathan T. Finnoff, DO, Jay Smith, MD, Department of Physical Medicine and Rehabilitation, Mayo Clinic College of Medicine, Mayo Clinic Sports Medicine Center, Rochester, MN

Although all chemicals have side effects most side effects are transient - they cease when the medication is discontinued - this is NOT the case with Cipro or its generic cousin Gentamicin !

Cipro, a 100% synthetic chemotherapeutic chemical, works by interfering with bacterial DNA, preventing it from replicating.

How can a synthetic chemical differentiate between bacterial DNA and your DNA!?

Cipro is a fluoroquinolone (also called "quinolone" or just "quin") class of chemicals.

Over HALF of all fluoroquinolone antibiotics have been pulled from the market for their horrific safety records - and those remaining (Cipro, Levaquin, Avelox and a few others) are no safer!

Every single chemical in this class carries a "black box warning" - the equivalent of a skull & crossbones.

Cipro's "black box warning" label makes it sound as if tendon rupture is the worst possible scenario.

Cipro is actually capable of unleashing an entire SYNDROME of systemic toxicity - "fluoroquinolone toxicity syndrome."

30-40 different adverse symptoms are suffered simultaneously and often last a lifetime.

Cipro-induced toxicity syndrome wreaks absolute havoc on every part of a person's body - every tendon and joint in the body can become affected, every organ (including the brain), peripheral nervous system, dystonia, muscle weakness, autonomic dysfunction, vision damage including temporary blindness, retinal tears and/or permanent double vision, permanent tinnitus, long lasting or permanent central nervous system damage (including relentless insomnia, memory loss, panic attacks, depersonalization, psychosis), chronic fatigue, multiple chemical sensitivities, severe muscle wasting, hair loss, skin changes, Sjörgren's syndrome, extensive dental damage …

Cipro is toxic to ALL connective tissues and the damage is cumulative.

Degeneration of the cartilage matrix in humans has been observed following as few as two oral doses of Ciprofloxacin.

People have also suffered osteonecrosis (bone death) as a result of chemotherapy.

Cipro is not even permitted for use in patients under the age of 18 because it can interfere with the development of a child's still-growing connective tissues. Cipro can render a top athlete of any age completely crippled and unable to walk, let alone workout or compete ever again.

Cipro is capable of causing severe delayed reactions that don't manifest until long after you've finished taking the chemical.

This means is that you could be experiencing a potentially permanent, crippling reaction to the chemical but have NO IDEA until it's too late! Your risk of spontaneously tearing or rupturing a tendon continues for up to FIVE YEARS after you have ingested the medication!

Cipro is also a neurotoxin capable of crossing the blood-brain barrier and causing severe long-term neuropsychiatric side effects.

These include panic and anxiety, relentless insomnia, seizures, confusion, depersonalization, psychosis, memory loss, paranoia and hallucinations.

These side effects can result from as little as ONE pill and persist for years or in some instances even be permanent!

Cipro can calcify all of the nerves in your teeth as well as permanently dry out your mouth, promoting extensive tooth decay and/or tooth loss.

The vast majority of physicians are completely ignorant about Cipro and its horrific and long-lasting side effects.

Most won't believe you when you tell them a prescription antibiotic has caused your slew of sudden disabling health problems - even if your symptoms match the ones listed right on the chemical's warning label!

Doctors often misdiagnose fluoroquinolone toxicity syndrome victims as having autoimmune disorders such as multiple sclerosis, since many Cipro-induced ADR's mimic those of autoimmune disorders.

Other favorite misdiagnosis include reflex sympathetic dystrophy (also called chronic regional pain syndrome or CRPS), fibromyalgia, chronic fatigue syndrome, scleroderma, Raynauld's syndrome, and Sjogren's.

There are natural plant based antibiotics.


Rhett, my cat, thought I was feeding him and jumped into the still wet insecticide so I grabbed him and he landed a claw in my middle finger knuckle joint (metacarpals/hamate) which became infected.

(Rhett passed away from lung cancer - and I know he didn't smoke!)

I ended up hospitalized.

First they give me a DPT shot and then three Gentamicin intravenous drips with follow up oral doses of Ciprofloxacin.

Gentamicin is an aminoglycoside antibiotic composed of a mixture of related gentamicin components and fractions and is used to treat many types of bacterial infections.

It is synthesized by Micromonospora, a genus of Gram-positive bacteria widely present in the environment (water and soil).

The drug binds avidly to certain tissues. Gentamicin can also be highly nephrotoxic, particularly if multiple doses accumulate over a course of treatment.

For this reason gentamicin is usually dosed by ideal body weight.

Various formulae exist for calculating gentamicin dosage.

Also trough and peak serum levels of gentamicin are monitored during treatment, generally before and after the third dose is infused.

Gentamicin, like other aminoglycosides, causes nephrotoxicity by inhibiting protein synthesis in renal cells.

This mechanism specifically causes necrosis of cells in the proximal tubule, resulting in acute tubular necrosis which can lead to acute renal failure.

Side effects of gentamicin toxicity vary from patient to patient.

Side effects may become apparent shortly after or up to months after gentamicin is administered.

Symptoms of gentamicin toxicity that I experienced included: balancing difficulty, ringing in the ears (tinnitus); difficulty multi-tasking, particularly when standing (anger breakdown at 149 over removal or leaving door).

Psychiatric symptoms related to gentamicin that I experienced included: confusion and disorientation.

Other side effects I experienced included: loss of appetite, a severe intestinal condition (Clostridium difficile-associated diarrhea enhanced with glyphosate) which may occur during treatment or weeks to months after treatment has stopped.

Many medical practitioners freely administer gentamicin as an antibiotic without advising patients of the severe and permanent potential ramifications of its use.

Gentamicin is well known to be a cheap, low-cost yet old medicine when compared with modern alternatives, and is typically US$3-6 per dosage less than modern alternatives.

Many people recover from gentamicin toxicity naturally over time if the drug is discontinued, but they recover slowly and usually incompletely.

Sometimes the toxicity of gentamicin can still increase over months after the last dose.

Upon cessation of gentamicin therapy symptoms such as tinnitus and imbalance may become less pronounced.

Do not use anti-diarrhea products or narcotic pain medications if you have any of the following symptoms because these products may make them worse:

diarrhea, abdominal or stomach pain/cramping, blood/mucus in your stool.

This is not a complete list of possible side effects.

Are You Taking This Dangerous Antibiotic?

Johnson & Johnson Faces $800M Levaquin Lawsuit

2004 Study published in New England Journal of Medicine systematically documents a dramatic increase of cardiac arrest associated with erythromycin use.

"This study shows the need for continuing research on the safety of older medicines, including how they interact with newer chemicals." - observer Wayne A. Ray, a professor of preventive medicine at Vanderbilt University School of Medicine in Nashville.

"Nobody realized the magnitude of the problem before." - Dr. Muhamed Sanc, cardiologist and director of the electro cardiology laboratory at the University of Medicine and Dentistry of New Jersey in Newark.

2008 30 million pounds of antibiotics are used in America each year.

Even though 25 million pounds are used in animal husbandry to promote growth, only 2 million pounds of those antibiotics are used for specific infections.

84% of salmonella is resistant to at least one antisalmonella antibiotic.

54% of Campylobacter jejuni are resistant to at least one anti-Campylobacter antimicrobial agent.

2013 US study shows 35% of anaphylaxis cases are caused by medications.

In the US drugs were the most common cause of fatal anaphylaxis accounting for 60% of all anaphylaxis-related deaths.

In the UK drugs are responsible for 42% of all identified causes of anaphylaxis.

In Latin America drugs are responsible for 31% of all anaphylaxis cases.

Ketek (telithromycin)

Telithromycin is a semi-synthetic erythromycin derivative.

It is forged by substituting a ketogroup for the cladinose sugar and adding a carbamate ring in the lactone ring.

FDA approved Ketek, patented by Sanofi-Aventis, in 2004 to treat severe infections.

The FDA submitted clinical trial data that key officials knew to be tainted by scientific fraud including fictitious patients.

Several users of Ketek experience liver failure.

unique library index

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