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Eschscholzia Californica

Eschscholzia Californica

 


Eschscholzia Californica (California poppy or gold poppy)

 

Overview

 

Eschscholzia californica (California poppy or gold poppy) is the state flower of California.  According the Department of Agriculture, the plant grows in the Spring, Summer, and Fall and reaches a height of about 1.2 feet at maturity. 

 

The seeds of the plant can produce sedative-like feelings, but the poppy falls into a different class of alkaloids than poppies used in strong narcotics. 

The USDA states that the Eschscholzia californica (California poppy or gold poppy) is an invasive species.  Currently, the plant is found in Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Georgia, Hawaii, Idaho, Kentucky, Louisiana, Maine, Michigan, Missouri, North Carolina, Nebraska, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin, and Wyoming.  The plant is also found in six different parts of Canada. 

 

Legal Issues Connected to Eschscholzia californica (California poppy or gold poppy)

 

In some states, it is illegal to cut down the state flower regardless if it falls on public or private land.  However, it is not illegal to cut down the state flower in California unless it falls on public lands or along state or county roads. 

 

The law concerning the removal of the state flower, and any other plants for that matter, is referenced in California Penal Code Section 384a.  The penal code is paraphrased below:

 

“Every person who within the State of California willfully or negligently cuts, destroys, mutilates, or removes any tree or shrub, or fern or herb or build or cactus or flower, or huckleberry or redwood greens, or portion. . .growing upon state or county highway rights-of-way [excluding highway employees]. . .[or] growing upon public land or upon land not his or her own. . .is guilty of a misdemeanor and upon conviction thereof shall be punished by a fine or not more than one thousand dollars ($1,000), by imprisonment in a county jail for not more than six months, or by both fine and imprisonment.”

 

In order to cut down and/or remove plants and tree from private property, the owner of the property must provide written and signed consent to the person removing the plants.  The same applies on public lands.  In order to remove plants along public highways or on public land, the person or entity must receive written consent from the government body. 

 

Medicinal Uses of Eschscholzia californica (California poppy or gold poppy)

 

According to the Florida Museum of Natural History, Native Americans have used the plant throughout history as a cosmetic, to kill lice, and even relieve mild pain and treat insomnia.  As of 2005, there were still pharmacological studies concerning the plant according to the Florida Museum of Natural History. 

 

The plant is still used as a recreational drug in some circles, and the federal government does not control the use of the plant.  As mentioned before, the plant does have relaxing qualities if ingested, but the effects are mild compared to pharmaceutical opiates. 

 

Sources:

1. https://www.leginfo.ca.gov/cgi-bin/displaycode?section=pen&group=00001-01000&file=369a-402c

2. https://plants.usda.gov/java/profile?symbol=esca2

3. https://www.flmnh.ufl.edu/flowerpower/poppy.html  

Roll Your Own

Roll Your Own

 


What is a Roll-Your-Own Cigarette?

 

A roll-your-own cigarette (RYO) is a cigarette that is made with loose tobacco and a rolling paper.  RYO products often include a bag of loose tobacco, and these pouches sometimes come with rolling papers as well.

Some smokers preferred RYO products because they were cheaper and it allowed them to receive more nicotine than manufactured products on the market.  However, the cost of these products has sky rocketed in since 2009 after President Obama signed a piece of legislation that provided tax exemptions for RYO products.  The president also signed a piece of legislation in 2012 that end tax exemptions for manufacturers of RYO cigarettes. 

 

Increased Taxes on Roll-Your-Own Products Since 2009

 

In 2009, Congress expanded the State Children’s Health Insurance Program, and the expansion partly possible because the program raised taxes on cigarettes by 158 percent.  The tax went from $19.50 per thousand cigarettes to $50.33 per thousand cigarettes.  Congress expected consumers, and especially teenagers, to switch to roll-your-own products after the tax hike, so they hiked taxes on RYO products as well. 

 

The taxes on RYO products increased from $1.10 per pound to $24.78 per pound, an increase of 2,159 percent.  Taxes on small cigars increased as well, from $1.83 per thousand to $50.33 per thousand—an increase of 2,653 percent.  The tax hikes were strongly supported by the Campaign for Tobacco-Free Kids, the American Medical Association, the American Cancer Society, and the American Lung Association.

 

Since the take hikes, RYO sales have decreased by as much as 74%, but pipe tobacco sales have increased by more than 10%.  Here’s why.  Taxes on pipe tobacco only increased by 158%, and taxes on large cigars only increased by 155%.

 

Many manufacturers of RYO products began to advertise their products as pipe tobacco to avoid the tax increase.  There has also been an increase in commercial RYO machines that allow consumers to purchase tobacco and then place it in the machine that can role about 200 cigarettes in only a couple minutes.  These initiatives have allowed RYO manufacturers to avoid increased taxes, but President Obama signed a bill in 2012 that redefined tobacco manufacturers. 

 

Numerous Roll-Your-Own Cigarettes Stores Going Out of Business

 

On July 6, 2012, President Obama made a small amendment in the Federal Transportation Bill that redefined a tobacco manufacturer.  The bill states that any business with a RYO cigarette machine now classifies as a tobacco manufacturer and is subject to the same taxes for packaged cigarettes. 

The bill was signed after the Government Accountability Office save a huge increase in pipe tobacco sales.  The increase was due to increased taxes on RYO tobacco, so many consumers started using pipe tobacco in their rolled cigarettes because pipe tobacco was taxed less. 

 

The bill has caused several businesses to close their doors because the RYO cigarettes machines were expensive and the investment never paid for itself in time.  Opponents of the bill claim that consumers will still find a way to find cheap tobacco. 

Two Indicted for Shipping Illegal Meds into US

Two Indicted for Shipping Illegal Meds into US


On November 7, 2012, the Department of Justice reported that two Pakistani nationals were indicted by a federal grand jury in the District of Columbia for operating websites that shipped illegal pharmaceuticals into the United States from Pakistan and the United Kingdom.  The two defendants are Sheikh Waseem Ul Haq and Tahir Saeed.  


The indictment shows that Ul Haq and Saeed operated and owned Waseem Enterprises and Harry’s Enterprises in Pakistan.  The two men are believed to have shipped about $2 million of illegal pharmaceuticals around the world and about $780,000 to the United States.  


The two defendants made U.S. customers submit payments by Western Union to people in Karachi, Pakistan so they could conceal the funds.  They also told U.S. citizens that U.S. customs officials may intercept the packages as they enter the United States.  


The illegal drugs include the following:


•    alprazolam (labeled as Xanex)
•    diazepam (labeled as Valium)
•    lorazepam (labeled as Ativan)
•    clonazepam (labeled as Klonapin)
•    numerous types of anabolic steroids and other controlled substances


The defendants are charged with conspiring to import illegal pharmaceuticals to the United States, conspiring to distribute controlled substances, conspiracy to using misbranded pharmaceuticals, importing and distributing controlled substances, and conspiracy to commit money laundering.  


The two defendants each face 20 years in prison for each count of the importing and exporting conspiracy, as well as 20 years in prison for the money laundering charge.  They face more time with other charges as well.  


Stuart F. Delery, Acting Assistant Attorney General for the Civil Division, stated: “This prosecution aims to curb the flow of dangerous drugs into the hands of United States citizens.  The drugs allegedly sold by the defendants were not approved for distribution in the United States, were not dispensed by U.S. licensed pharmacies, and were not prescribed by any physician.”


Source: Federal Bureau of Investigation
 

Xarelto Approved to Treat and Reduce Blood Clots

Xarelto Approved to Treat and Reduce Blood Clots


On November 2, the Food and Drug Administration (FDA) approved Xarelto (rivaroxaban) to treat deep vein thrombosis (DVT) and pulmonary embolisms (PE), as well as to reduce the risk of DVT and PE after a surgery or treatment.  


DVT is a serious type of clot that occurs when blood thickens in a deep vein of the body.  These types of clots are most common in the lower leg and the thigh and are extremely dangerous if they break off.  They can travel to an artery in the lungs and can restrict blood flow—possibly leading to the PE which is deadly.  


The drug was already approved by the FDA and used after knee and hip replacement surgeries.  The drug was also used to reduce the risk of stroke in people with an irregular heartbeat called non-valvular atrial fibrillation.  


Richard Pazdur, M.D., states: “Xarelto is the first oral anti-clotting drug approved to treat and reduce the recurrence of blood clots since the approval of warfarin nearly 60 years ago.  Pazdur is the director of the Office of Hematology and Oncology Products at the Drug Evaluation and Research Center for the FDA.  


Other drugs that are approved to reduce the risk of blood clots include the following: Lovenox (enoxaparin), generic enoxaparin, Arixtra (fondaparinux), Fragmin (dalteparin), Coumadin (warfarin), and heparin.  


In clinical studies, only about 2.1 percent of patients taking Xarelto and 1.8 percent to 3 percent of patients taking enoxaparin and other combinations had a recurrent DVT or PE.  A specific study showed that 1.3 percent of patients taking Xarelto had a recurrent DVT or PE compared to 7.1 percent of patients taking a placebo.  


The main side effect of Xarelto is bleeding or uncontrolled bleeding.  These side effects are common with anti-clotting medicine.  


Source: U.S. Food and Drug Administration

Leader of Indianapolis Drug Organization Gets 10 Years

Leader of Indianapolis Drug Organization Gets 10 Years


On November 7, 2012, Immigration and Customs Enforcement (ICE) announced that Agustin Lozano was sentenced to 10 years in prison for leading a drug trafficking organization that ran drugs between Mexico and Chicago.  The investigation was led by ICE’s Homeland Security Investigations (HSI), the DEA, the IRS’s Criminal Investigation Division, and the Indianapolis Metro Drug Task Force.  


Lozano is a Mexican national, and he was sentenced on November 6, 2012 before U.S. District Judge William T. Lawrence with the Southern District of Indiana.  Lozano pleaded guilty to drug trafficking and money laundering, and he’ll be turned over to the ICE after he serves his prison sentence to face deportation.  


Starting in July of 2010, undercover agents started working with Lozano.  An undercover agent bought three grams of cocaine for $150 initially.  It took eight months to coordinate the investigation and gather information between agencies, and 48 kilograms of cocaine were eventually confiscated on December 15, 2010.  The cocaine had an estimated street value of $1.5 million.  Authorities confiscated 4.4 pounds of methamphetamine as well.  The methamphetamine had an estimated street value of $80,000.  


Throughout the investigation, it was found that the criminal organization distributed about five pounds of methamphetamine and 10 kilos of cocaine throughout Indianapolis every month.  184 pounds of marijuana, $69,500 in cash, and 18 firearms were confiscated during the investigation as well.  


U.S. Attorney Joseph H. Hogsett stated, “This sentence is an example of proactive and cooperative anti-drug police work at its finest.  A drug bust of this significance occurs only once every couple of years.  Let the message be heard loud and clear to all those who seek mayhem by trafficking in illegal narcotics – you will be identified, you will be investigated and you will be prosecuted to the fullest extent of the law.”


Source: U.S. Immigration and Customs Enforcement

Advair Diskus 250 50 Price

Advair Diskus 250 50 Price

A Brief Overview of the Advair Diskus 250 50 price

Patients with respiratory conditions such as emphysema or asthma may be prescribed Advair Diskus. Although expensive, several pricing options must be considered to achieve a lower Advair 250 50 price.

Before prescribing this medication, a physician's office will contact your insurance company if you are uncertain as to whether your policy can cover part or all of the Advair Diskus 250 50 price. Depending on your policy, the total cost incurred by the Advair 250 50 price may be covered completely or up to a certain point. If you suffer from asthma, keep in mind that this drug is only indicated for short-term use. Therefore, you may be able to determine the final bill for a fixed course of treatment after learning what the Advair Diskus 250 50 price is from a trusted provider.

While patients who live in an area with multiple pharmacies may be quoted more than one Advair 250 50 price, these may not be low enough to fit their budget. Likewise, patients in rural areas  may wish to shop online to locate a pharmacy which lists its Advair Diskus 250 50 price. Buying medication online is not a process to be undertaken casually. Consult with your physician to see if they are aware of any reputable online pharmacy which may list a suitable Advair 250 50 price.

No matter how low the listed Advair Diskus 250 50 price, do not purchase medication from any online pharmacy which does not require a prescription to make a sale. Websites which offer Advair 250 50 price without a prescription are not operating in accordance with the law. Because they have already demonstrated a willingness to break the law, they cannot be trusted with your credit card information.

To help decrease the Advair Diskus 250 50 price, the manufacturer is currently offering a coupon which removes $10 from every monthly purchase. This coupon to lower the Advair 250 50 price must be printed out and presented along with a prescription at a pharmacy. Additionally, at this time the manufacturer is currently offering a free 30-day trial dose to patients with a prescription. Such offers of assistance in lowering the Advair Diskus 250 50 price are constantly changing and contain many restrictions. You should also ask your doctor if they have any coupons which can lower the Advair 250 50 price.

You should be confident that you are receiving what you paid for regardless of the Advair Diskus 250 50 price. If medication you purchase turns out to be incorrectly dosed or otherwise defective, a pharmacy may be liable for damages if adverse effects ensue. Maintain receipts of any purchase recording the Advair 250 50 price paid. These will be necessary for a lawyer to determine how much compensation you should seek if litigation is likely to result in success.

 

Mushroom

Mushroom

What Makes a Mushroom Illegal?
There are many different plants and mushrooms that contain hallucinogenic compounds that have been used for centuries, mostly during religious rituals. In hallucinogenic mushrooms (sometimes called magic mushrooms or shrooms), a compound called psilocybin, or 4-phosphoryloxy-N,N-dimethyltryptamine, is responsible for these effects. These mushrooms are often found in sub-tropical regions of Mexico, South America, and the United States.
Mushrooms with psilocybin cannot be inactivated by cooking or freezing and when ingested, the activated form of psilocybin, psilocin, can appear in the body within 20 minutes cause hallucinations that last for around six hours.
The hallucinations caused by mushrooms can be described as strong distortions of the perception of reality, for example hearing, seeing, and feeling things that are not there. It can also cause strong emotional swings. These effects are caused by psilocybin’s ability to disrupt the proper function of serotonin, a neurotransmitter, and its interaction with nerve cells in the central nervous system.
Aside from hallucinations, psilocybin can also cause lack of muscle tone or muscle weakness, ataxia, nausea, pupil dilation, drowsiness, and vomiting. These side effects are particularly visible when taking psilocybin as a pure dose between 10 to 20 mg.
While a pure dose of psilocybin has relatively predictable results, mushrooms are most commonly consumed by preparing hem either dried or brewed. Doing so makes the effects of the chemicals much less predictable. In this situation, the age of the mushroom as well as how well it is preserved acts as a determinant for the effects.
According to the United Nations 1971 Convention on Psychotropic Substances, psilocybin is listed as a Schedule I drug but is not covered by any of the UN drug treaties.
In the United States, possession of these hallucinogenic mushrooms is illegal. Under the Controlled Substance Act, psilocybin is considered a Schedule I substance, alongside other drugs such as LSD and heroin. These mushrooms have very little if not a complete lack of legitimate medical purpose yet a high potential for abuse.
Unlike the mushroom, the spores do no contain any psilocybin and are this legal in the majority of States, with the exception of Georgia, California, and Idaho. However, these spores cannot sold if used for the purpose of cultivating hallucinogenic mushrooms. California further bans selling, trading, importing, buying, or giving away the spores.
All states except New Mexico consider growing psilocybin containing mushrooms to be illegal. While New appeals court ruled that growing psilocybin containing mushrooms for personal use could no be classified as manufacturing a controlled substance, federal law still makes it illegal.

Depo-Provera

Depo-Provera

 

What is Depo-Provera?

Depo-Provera is the brand name of depot medroxyprogesterone acetate which is a drug that prevents pregnancy. It is manufactured and distributed by the Pfizer Corporation. It is administered via an injection and protects against pregnancy for three months. It is highly successful at preventing pregnancy and requires less drug interaction than once-daily birth control pills. For this reason, Depo-Provera’s status a as long acting reversible contraceptive is highly desirable for many that cannot maintain a contraceptive regimen such as with birth control pills.

Where can I get a Depo-Provera shot?

Most medical providers and some organizations such as Planned Parenthood have the shots available. It is the responsibility of the patients to regularly schedule the shots and to be aware of the potential risks of using the shot. In addition to the benefits, there are side effects that may prohibit some women from taking this shot.

How does Depo-Provera work?

The Depo-Provera shot works by releasing the hormone progestin into the body which works on the ovaries to prevent them from releasing egg and increasing vaginal mucous to inhibit pregnancy. This is effective for 99 out of 100 women that receive the shot. There are some side effects including irregular menstrual periods, depression, dizziness and acne and most importantly, loss of bone density.

What is the controversy around the use of the Depo-Provera shot?

As Depo-Provera has been found to decrease bone-density women with a history of or risk factors for osteoporosis should not receive this shot as it will exacerbate this condition. All women will need calcium and vitamin D while on this shot. Still, others have made the claim that the bone density loss that accompanies the shot is not articulated properly to women that receive the shot and that the bone density loss is irreversible.

What should I do if I have experienced bone density loss?

Bone density loss can lead to a number of injuries and an increase of potential injuries. If you feel that you were not provided adequate notice of the dangerous of bone loss, you may be able to hold the provider or manufacturing company liable for damages. As in all liability cases, the victim must prove that that injury or harm was on cause on the part of the provider and that the provider was aware of the potential harm but chose not to inform the plaintiff about the danger. Especially in cases with bone loss, the harm is potentially irreversible and imperils their ability to have children or live a healthy life.

Speak with an attorney if you feel you have not been adequately warned or you feel your medical provider is liable for failing to inform you of the potential risks of using this medication.

Fen-Phen

Fen-Phen

What is Fen-Phen?
 
 
Fen-Phen is a drug combination that consists of fenfluramine and pherntermine and was used to treat obesity. It has since been withdrawn from the market. At first, the drug was found to be useful against obesity and hailed as a “diet miracle”, although patients were found to relapse after stopping treatment. Eventually the drug was found largely ineffective at helping weight loss, only improving the mood of the patient and increasing dependency on a mood altering medication.
 
 
How does Fen-Phen work?
 
 
Fenfluramine releases more serotonin into the body, tricking the body into feeling full. The downside is that the increase in serotonin has cause psychotic episodes and other undesirable mental disorders. Adding pherntermine to the fenfluramine was thought to counteract the harmful psychological effects of serotonin imbalance and this drug combination was done “off label” or unapproved by the Food and Drug Administration. Fen-Phen was intended to affect the serotonin receptor that made the patient feel full, but it also stimulated another receptor that led to problems with the heart. This is known as neurotoxcity and was unaccounted for in studies about the affect Fen-Phen has on the body.
 
 
What are the risks associated with taking Fen-Phen?
 
 
There were early indications that fenfluramine caused pulmonary hypertension or the thickening of the lungs that in turn affects proper breathing. Nonetheless, a variation of the drug, brand named Redux was approved and sold to American consumers until the FDA announced its withdrawal in 1997. There were additional concerns about the effect of the drug on heart valves with as many as 66 cases of disease in patients that had been taking fenfluramine and its variants.
 
 
What has been the liability, assessed to date?
 
 
Wyeth pharmaceuticals (now owned by Pfizer), the distributor of fenfluramine and Redux has an estimated liability of 14 billion owed to individuals that have suffered from taking Fen-Phen. There has been dispute as to the amount of individuals affected by cardiac distress by this drug with some estimates ranging as high as thirty percent. Studies have shown that individuals that have taken this drug for more than two years have a 17% increased chance of developing heart valve disease.
 
 
What should I do if I have been negatively impacted by this drug?
 
 
An electrocardiogram from a licensed healthcare provider is essential to failing a claim for your share of the settlement. Disbursement of compensation had slowed after falsified or misleading electrocardiograms were submitted for claims by doctors that were paid by law firms. An attorney can better help you determine if you are eligible for damages due to medical expenses, loss of wages and pain and anguish.