Beacon of Hope – Life-Saving Drugs in the Darkness

A psychedelic storm is brewing. You have taken MDMA, DMT, psilocybin, and a mysterious compound called kanna.

You and your friends are on a spiritual journey to access higher levels of consciousness, reunite with your inner self. During this trip, you are equipped with harm reduction kits. These kits contain clean needles, offering a glimmer of hope in the darkness of addiction; condoms, safeguarding the body; and naloxone, life-saving overdose antidote.

Temozolomide
Temozolomide (pronounced tem-oh-zohlo-mide) is an antineoplastic drug used to treat specific types of brain cancer (such as glioblastoma multiforme, or GBM) in patients whose tumors have recurred after previous treatment or who have not responded to other treatments. It is also being studied in other types of cancer. Temozolomide belongs to a group of medicines called alkylating agents. It interferes with the growth of cancer cells by blocking the formation of DNA molecules. Because normal body cells can also be affected, side effects may occur.

The mechanism by which Temozolomide manufacturer works is not fully understood. However, it is thought that the drug prevents cancer cells from producing DNA by preventing them from attaching to other molecules on which they depend for survival. The drug is converted to an active molecule in the cell, MTIC, which then methylates DNA on the N7 position of guanine (N7-MeG), the N3 position of adenine (N3-MeA), and the O6 position of guanine (O6-MeG). The methylated DNA prevents cellular repair mechanisms from correcting the damaged DNA, causing the cells to die.

A recent clinical trialExit Disclaimer found that temozolomide significantly improves survival in patients with recurrent GBM when combined with cisplatin and docetaxel. The combination reduced the median time to progression by more than three months. The findings were published in The New England Journal of Medicine. In another study, a combination of temozolomide and thalidomide (an antineoplastic that inhibits cell division) improved survival in patients with recurrent GBM. The combination reduced the median time to progression to less than four months, and increased objective responses (such as complete response or partial response) to 25 per cent.

When administered orally, temozolomide comes as capsules that are taken by mouth on a set schedule, usually once per day at bedtime. It should be swallowed whole and on an empty stomach (1 hour before or 2 hours after a meal) to help prevent nausea. It is important to take the medication at the same time each day, and not to miss doses.

Before starting temozolomide, it is important to tell the doctor about any allergies or other medical conditions, including liver or kidney problems or bleeding issues. It is also important to tell the doctor if the patient has any infections or is receiving any other medications, including antiepileptics. Temozolomide can make the patient more susceptible to infection, so it is important that patients avoid contact with people who have contagious diseases such as flu or measles.

Gefitinib
Gefitinib is an oral medication that works to stop cancer cells from growing in order to treat advanced non-small cell lung cancer (NSCLC). It may be given alone or with other treatments such as surgery, radiation, and chemotherapy. It is important to tell your doctor if you have other medical conditions before starting Gefitinib manufacturer.

This drug works by inhibiting the epidermal growth factor receptor tyrosine kinase, which causes cancerous cells to grow and divide too quickly. This drug is typically used in patients whose tumors have specific types of EGFR mutations, which have been identified by genetic testing. Your oncologist will test your tumor for these abnormalities before prescribing this medication.

Although gefitinib is a powerful drug that can achieve tumor regressions in NSCLC, it has a number of serious side effects. One of these is pulmonary toxicity, which can cause symptoms such as shortness of breath and coughing up blood. This complication can be fatal if not treated quickly.

Symptoms of pulmonary toxicity usually start at about two weeks after the beginning of treatment and are rapidly progressive. They often resemble those of atypical interstitial lung disease (ARDS) and are characterized by diffuse bilateral pulmonary opacifications. Gefitinib is more likely to cause pulmonary toxicity in older adults, women, smokers, and those with preexisting underlying pulmonary fibrosis.

Patients with a history of esophageal or colon cancer are also at increased risk of gastrointestinal and genital tract complications, including bowel obstructions. In addition, patients with liver or kidney disease are at greater risk of hepatotoxicity. This medication can also cause other serious side effects, such as liver failure.

Gefitinib is available in tablet form and should be taken by mouth once daily. Follow the directions on your prescription label carefully and ask your doctor or pharmacist to explain any part you do not understand. Take gefitinib exactly as directed. You may be given gefitinib through a nasogastric tube, but ask your doctor if this is safe for you. You will need to have frequent blood tests while taking this drug. These will check your levels of certain blood cells and how well your liver and kidneys are working.

Rucaparib
Rucaparib (Rubraca) is an oral inhibitor of poly-ADP-ribose polymerase 1, 2, and 3 (PARP) that prevents cancer cells from repairing damaged DNA. It is an important addition to the arsenal of drugs targeting PARP in gynecologic cancers, where genetic alterations that impair DNA repair are common. It has been shown to be effective in patients with BRCA-mutated ovarian and fallopian tube cancers and a plethora of other types of gynecologic malignancies.

https://www.specialitymedz.com/product/rucaparib-manufacturer/ was approved by the FDA on April 6 as a maintenance therapy for women with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who have a platinum-sensitive tumor and who have undergone at least one prior line of chemotherapy. It joins olaparib (Lynparza) and niraparib (Zejula) as the third PARP inhibitor to be approved for this use.

The ARIEL3 trial, which examined the effectiveness of rucaparib in a subset of patients with high-grade ovarian carcinoma who had undergone previous PARP inhibitor treatment, was the first large, prospective study to show exceptional benefit among patients with recurrent ovarian cancer based on a molecular endpoint. The drug also was associated with an improved PFS in this group of patients, even when taken as a single agent.

These findings add to a growing body of evidence that PARPi therapy may benefit patients with certain tumors who have specific mutations in their BRCA genes or other genetic alterations that impair DNA repair, explains Fatima Karzai, M.D., clinic chief of the Genitourinary Malignancies Branch in NCI’s Center for Cancer Research. These patients are often excluded from clinical trials that have extensive exclusion criteria, she says.

In the ARIEL3 study, patients with a BRCA-mutated tumor were more likely to experience exceptional benefit than those with non-BRCA-mutated disease, which was the same as in earlier studies of this drug in the setting of ovarian cancer. But the differences weren’t as large as in other BRCA-mutated gynecologic cancers, and the overall PFS improvement was similar across all subsets of the population studied.

Rucaparib can cause serious side effects, including severe liver problems, and the dose should be reduced for those with hepatitis C or uncontrolled bile duct disorders. It can also affect the levels of minerals and salts in your blood, so you should drink plenty of fluids – around 2 liters (3 1/2 pints) per day – while taking it. Tell your doctor and pharmacist if you are allergic to this drug or any other medications, foods, or supplements.

Harm Reduction Kits
Harm reduction is an approach that promotes a holistic vision of human life and well-being, while also challenging stigma. It recognizes that substance use is a continuum of behaviors, seeks to eradicate the stigmatization of people who have been exposed to drug related harm, and encourages evidence-based practices. It recognizes the role of poverty, class, race, trauma and sex-based discrimination in the vulnerability of people to drug related harm and offers solutions that address those inequities.

In addition to syringes, the kits contain sterile water, cotton, a tourniquet and condoms. Originally, the kits were intended to include glass crack pipes, but because of the concern that the pipes could be used to spread blood-borne infections, they were removed from the kit.

The kits are distributed in a small hospital in Toronto, Ontario. Clinicians report that they have been very well received by patients, and they have helped to increase the willingness of clinicians to discuss harm reduction strategies with their clients. Clinicians have also reported that having the kits available has facilitated more open dialogue about drug-related harms, including overdoses and HIV-related health risks.

Toward the Heart is a non-profit organization that works to create and support harm reduction initiatives and communities. Its projects range from community-based peer engagement to advocacy work and coalition building. Its mission is to inspire and empower individuals, communities and faith groups to become active advocates for a societal change in the way we view and talk about addiction and recovery.

According to Lieutenant Nicholas Marcucio, when someone is detained at the police department, they are offered a harm reduction kit, along with literature about free recovery programs in New Haven. The kit includes a map of the city and a list of services for those who need help. Each bag has a unique identifier, which allows the police to track whether the person who receives the kit goes on to access recovery services.

The program is not without challenges, however. One challenge is the difficulty of obtaining funding for the kits. Another is the need to ensure that the naloxone and other medications are available when needed. Despite these obstacles, the program has been successful in increasing naloxone distribution and reducing overdose deaths. It has also contributed to a more positive perception of the police department.

Beacon of Hope – Life-Saving Drugs in the Darkness