Beginning as a prescription drug for severe or chronic pain, oxycodone gradually becomes a silent addiction. The patients may experience less pain and a high, ultimately creating a desire for more medication. After the initial first week, the desire has moved from a simple want to a need. The body begins to crave more, as the patient desires to feel the high again. After the first few weeks of being addicted, the original dosage no longer helps.
 Pantoprazole belongs to proton pump inhibitors (PPIs) class of drugs. PPIs acts on parietal cell, lies with them are proton pump which secrete H+ ion and this class of drug irrepressibly inhibit proton pump and thus, decrease acid production.  Majority of studies found that all PPIs are similar in their effectiveness, over recommended treatment period.  PPIs are also proven and effective to heal any damaged inner lining of food pipe.  PPI are first line of choice in moderate to severe GERD.
Pitavastatin is slightly unstable in light and hygroscopic. Each film-coated Pitavastatin tablet contains 1.045 mg or 2.09 mg, or 4.18 mg of pitavastatin calcium, which is equivalent to 1 mg or2 mg or 4 mg, respectively of free base and the following inactive ingredients: lactose monohydrate, hypromellose, magnesium stearate,magnesium alumina meta silicate, low substituted hydroxylpropyl cellulose and film coating containing the following inactive ingredients: titanium dioxide, hypromellose, colloidal anhydrous silica and triethyl citrate. 2.2 Mechanism of Action and Pharmacology: Pitavastatin drug competitively inhibits HMG-CoA reductase enzyme, which is a rate-determining enzymeinvolved in the biosynthesis of cholesterol, in the manner of competition with a substrate sothat it inhibits cholesterol synthesis process in liver. As a result of it, the expression of LDL-receptorsand followed by the uptake of the LDL from blood to liver is accelerated,and then the plasma TCdecreases. Further, the sustained inhibition of the cholesterol synthesis in liver decreaseslevels of VLDL(very low density lipoproteins).
It is a plastic flexible ring that is inserted into the vagina which releases hormones. It is left insides the vagina for three weeks out of a four-week menstrual cycle and releases estrogen and progestin in the body (Smith source 3). When the ring is used properly, less than one percent of women experience an unintended pregnancy (Smith). Advantages of the patch reduces bone thinning and protects a woman from Pelvic inflammatory disease and an ectopic pregnancy (Smith). The patch also makes periods lighter and more regular, decreases cramps and acne, and ovarian and uterine cancer are less likely to occur but also makes a woman more vulnerable to get blood clots (Source 6).
Ambien is a non-benzodiazepine drug that acts as one by binding selectively to GABA receptors. Ambien (zolpidem) is a sedative, also called a hypnotic. Zolpidem affects chemicals in the brain that may be unbalanced in people with sleep problems insomnia). Ambien is used to treat insomnia. Nervous system side effects most frequently have included visual disturbances, ataxia, and dizziness.
The elimination half-life of Secobarbital in children is 2.7 to 13.5 hours. Secobarbital is found to have an elimination half-life of approximately 30 hours in adults. The drug has also been found to have a plasma half-life of 15 to 40 hours (mean 28 hours) in adults. Toxicity The drug is known to cause adverse reactions such as somnolence, agitation, hypoventilation, bradycardia, and headaches. Taking Secobarbital with alcohol or other CNS depressants has been shown to have the ability to increase the danger of complex behaviors and have the negative effect of producing additive CNS-depressant
4. Molecular Diagnosis Parasite nucleic acids are identified by using the polymerase chain reaction (PCR). Even though this technique may be somewhat more susceptible than microscopy, it is of restricted effectiveness for the diagnosis of acutely ill patients in the standard healthcare setting. PCR results are often not obtainable rapidly enough to be of value in establishing the diagnosis of malaria infection. PCR is mostly beneficial for verifying the species of malarial parasite after the diagnosis has been recognized by either microscopy or RDT.
It is in a class of medication called glycopetide antibiotics. Biological half-life 4h to 11 h for adult. Action: The medication acts by inhibits cell wall synthesis. It is an alternative drug for staphylococcal and streptococcal infections, including endocarditis when allergies prelude the use of penicillin and cephalosporin Indication for Use: Potentially life threatening serious infections that include bone, skin, lower respiratory tract, and c. difficile Therapeutics Dosage: Vancomycin can be administering orally or intravenously. It is usually taken 3-4 time a day for 7-10 daysThe dosage is based on the patient m medical condition and response to treatment.
It delivers the vaccine into the muscle in about a tenth of a second. Kathy Callender states that “Needleless vaccines will likely generate the most efficient results in preventing muscle pain.” Another benefit of the needleless flu shot would be the prevention of contamination. The nasal spray vaccine reduces the possibility of cross-contamination. The needleless flu shot is offered to people who dislike
People are under the impression that after receiving the flu vaccination, they can essentially get influenza, however, it is not true. The vaccine is made from an extremely weakened form of the flu virus. (10 Flue Shot Pros & Cons to Help Decide If It 's For You) Health officials are claiming that if choose to be vaccinated for the flu, they have a nasal spray that can be administered instead of having an injection and it is just as effective. Likewise, it is approved for people ages 2 to 49. (10 Flue Shot Pros & Cons to Help Decide If It 's For You) On a positive note, if in favor of becoming vaccinated, they are available at most pharmacies, grocery stores, walk in clinics and some employers are offering them.