Azulfidine - a medicine with antimicrobic and antiinflammatory properties. It is taken at ulcer colitis, an ulcer proctitis, a pseudorheumatism, Crohn's disease. After reception Sulfasalazinum - it is observed the normal intestinal microflora, and as result of the molecule of active ingredient breaks up to compound components: sulphapyridine and 5-aminosalicylic acid. These substances have antibacterial and antiinflammatory activity. Antiinflammatory effect of 5-aminosalicylic acid thanks to low ability to absorption is defined generally in walls of a large intestine. Sulphapyridine has generally systemic antiinflammatory effect due to better absorption.
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500mg × 30 Pills | $0.92 | $27.66 + Bonus - 4 Pills | - | Add to cart |
500mg × 60 Pills | $0.71 | $42.74 + Bonus - 4 Pills | $12.60 | Add to cart |
500mg × 90 Pills | $0.64 | $57.83 + Bonus - 7 Pills | $25.20 | Add to cart |
500mg × 120 Pills | $0.61 | $72.92 + Bonus - 7 Pills | $37.20 | Add to cart |
500mg × 180 Pills | $0.57 | $103.09 + Bonus - 11 Pills | $63.00 | Add to cart |
500mg × 270 Pills | $0.55 | $148.35 + Bonus - 11 Pills | $99.90 | Add to cart |
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Azulfidine Product Description
Drug Uses
Azulfidine is an anti-inflammatory drug with a strong immunomodulating activity. Azulfidine is effective in treatment of rheumatic diseases and bowel inflammation in children aged 6 years and older and adults.
Azulfidine pills can be indicated for:
treatment of active Crohn's Disease;
induction and prolongation of the remission of mild, moderate, or severe ulcerative colitis;
treatment of polyarticular juvenile rheumatoid arthritis;
treatment of active rheumatoid arthritis in adults, when first-line treatment with non-steroidal anti-inflammatory drugs (including salicylates) has failed.
Missed dose
If you miss a dose of the anti-inflammatory drug, take Azulfidine pills when you remember it, but not if it is the time to take the next scheduled dose. Never take a double dose of Azulfidine.
If you miss the evening dose, take Azulfidine pills immediately after waking up. However, if you remembered about the missed evening dose when you have to take the morning dose, do not double an Azulfidine dose, just return to the prescribed dosage regimen.
More Information
Azulfidine can be used as adjuvant therapy combined with corticosteroids and dietary measures in acute attacks and relapse of ulcerative colitis. Azulfidine significantly improves joint mobility in 4-8 weeks after starting application.
Therefore, in the first few months of Azulfidine use, NSAIDs and /or analgesics can be indicated to the patient to maintain the anti-arthritic effect and relieve arthritis pain.
Storage
To protect Azulfidine tablets from light and moisture, they are recommended to be kept in a dry place, in original package, at temperature not below 15°C.
Azulfidine Safety Information
Warnings
Azulfidine use should be stopped if the patient during the anti-inflammatory therapy experiences symptoms of or have been diagnosed with kidney abnormalities, liver diseases, hematological disorders, infectious diseases, or severe allergies. For early diagnosis of potential risk factors in the first months of Azulfidine use, the patients may be advised to periodically undergo blood tests, urinalysis, and other laboratory and diagnostic tests.
Disclaimer
Information about Azulfidine is provided for informational purposes only and not intended to substitute the consultation with the gastroenterologist and/or rheumatologist. The online pharmacy shall assume no responsibility for any loss, omissions, or damage caused by as a result of using the information about this anti-inflammatory and immunomodulating drug.
Azulfidine Side Effects
Azulfidine may cause loss of appetite, fatigue and nausea in the first days of the inflammatory therapy. The long-term application of Azulfidine may cause weight loss, headache, or vomiting in about 30% of patients.
Some men may complain of the decreased ejaculate volume because of Azulfidine use. Approximately 3% of patients, after Azulfidine intake, may experience allergy and haematological disorders. High daily doses of Azulfidine are most likely to cause adverse gastrointestinal effects comparing to minimal maintenance doses of Azulfidine.
If initial doses of Azulfidine cause serious gastrointestinal effects, the patient is recommended:
- To stop taking Azulfidine pills (resume them within 5-7 days after withdrawal).
- To cut the daily dose of Azulfidine in half (followed by gradual increase in the dose within 2-3 days).
- To switch ordinary Azulfidine pills to Azulfidine EN-tabs (medications with sustained-release active ingredient).
Starlix - an oral synthetic hypoglycemic drug. A medicine based on nateglinide for the treatment of diabetes, which helps to control blood sugar levels. This medicine helps your body to react better to the insulin produced by your pancreas.
Starlix is used in conjunction with diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus.
Furosemide - «Loopback" diuretic; causes quickly coming, severe and short-term diuresis. Has natriuretic and chloro effects, increases clearance of K+, Ca2+, Mg2+. It is taken at edematous syndrome, cirrhosis, diseases of kidneys, heavy course of arterial hypertension and hypercalcemia.
Capoten suppresses activity of angiotensin-converting-enzyme therefore angiotensin-I turns into angiotensin II - substance which has strong vasoconstrictive action. Capoten reduces secretion of Aldosteronum in suprarenal cortex, at the same time the delay of sodium and water in an organism decreases. Capoten slows down process of bradykinin destruction and promotes increase of E2 prostaglandin, and also nitrogen oxide that causes vasodilating action. Thanks to these effects it is decreased the increased arterial pressure, the general peripheric resistance decreases, pressure in the right auricle, in a small circle of blood circulation decreases and cordial emission increases.
A semi-synthetic antibiotic from the macrolides group for oral administration. The list of indications includes: infections of the upper and lower respiratory tract (pharyngitis, bronchitis, pneumonia, bacterial infection in COPD, panbronchiolitis, bronchiectasis), respiratory tract (tonsillitis, sinusitis, otitis media), skin and soft tissues (erysipelas, phlegmon, furuncles, folliculitis, impetigo, pyoderma), urinary tract (urethritis, endometritis, cervicitis, vaginitis, including sexually transmitted infections, except gonorrhea), oral cavity (periodontitis), bones (periostitis, chronic osteomyelitis); scarlet fever, diphtheria, whooping cough, trachoma, migratory erythematous rash, brucellosis.
Forxiga is the drug produced in the form of tablets. Tablets belong to SGLT2 inhibitors. Its main purpose is to reduce the level of blood sugar. It helps the kidney to remove glucose from the organism and excrete it during urination. It also helps to lose weight. Patients use the tablets to treat type II diabetes and get rid of the additional weight that is the result of the health disorder. The drug can be taken alone as a monotherapy or as an additional treatment. It doesn’t fit people with diabetes I.
The antifungal agent which has activity against dermatophytes, yeasts, dimorphic fungi and eumycetes. It is also active against staphylococci and streptococci. The therapeutical indications of the drug include: mycoses of the gastrointestinal tract, eyes, genital organs, chronic recurrent vaginal candidiasis, dermatomycosis, onychomycosis, Candida, folliculitis, dermatophytosis, systemic fungal infections (blastomycosis, candidiasis, paracoccidioides, coccidioidomycosis, cryptococcosis, histoplasmosis, hromomikoz, sporotrichosis, paronychia, fungal sepsis, fungal pneumonia); leishmaniasis; tinea versicolor, prevention of fungal infections in patients with a high risk of their development. The mechanism of action is inhibition of fungal membrane ergosterol synthesis and the violation of the cell wall permeability.
It has a direct influence on muscles, mainly of arterial vessels over nitric receptor situated in blood vessels. Its active component is transformed into oxide in smooth muscles that effect prompts the activity of guanylate cyclases. It is crucial for the creation of cyclic guanosine monophosphate (relaxation mediator). The drug influence the processes in the central vascular system and heart activity. The nature and force of the influence of nitroglycerin on the cardiac organ and vessels depend on the cooperation of essential actions.
Kamagra Effervescent - a cutting-edge invention in a pharmacological niche when one has given an idea to release the ED Generic in the form of instant polos that turn an ordinary drinking water into a marvelous orange juice drink. This format permits one to perceive the intake of the pharmaceutical as a real pleasure.
Kamagra - a pharmaceutical remedy for the readiness of a male sexual organ for a sex, provided by the generics maker named Ajanta, perceptibly balances the male aplomb and is one of the best replacements of Viagra.
Florinef is a brand name of Fludrocortisone. It is a corticosteroid produced to treat adrenogenital syndrome (also called Apera-Galle syndrome), Addison's disease, orthostatic hypotension, cerebral salt wasting syndrome, and adrenal insufficiency. The drug replenishes the deficiency of hormones of the adrenal cortex. 1 tablet contains 0.1 mg of fludrocortisone acetate. It participates in the metabolism, including mineral and carbohydrate one. The drug causes the retention of sodium ions and promotes the excretion of potassium.
Blocks the final stage of HCl secretion, reducing basal and stimulated secretion, regardless of the nature of the stimulus. Prescribed for gastric ulcer and duodenal ulcer in acute phase, erosive-ulcerative esophagitis, reflux esophagitis, Zollinger-Ellison syndrome, stress ulcers of the gastrointestinal tract; eradication of Helicobacter pylori within a combination therapy, non-ulcer dyspepsia.
An antimicrobial bactericide - synthetic derivative of nitroimidazole. Used in urethritis, vaginitis, intestinal amoebiasis, liver amoebiasis, giardiasis.
is given to patients for treating severe acne that do not respond to other medicines
Etodolac - has an anti-inflammatory, analgesic, antipyretic effect. The medicine is prescribed in case of rheumatoid arthritis, ankylosing spondylitis, arthrosis with pain syndrome and restriction of movements, acute and chronic osteoarthritis.
Elavil - antidepressive medicine. Renders also some analgesic, H2-histamineblocking and antiserotonin action, promotes elimination of bedwetting and reduces appetite. It is taken at Depressions (especially with anexiety, agitation and sleep disorders, including children's age, endogenous, involutional, reactive, neurotic, medicinal, at organic lesions of a brain, alcoholic abstinence), schizophrenic psychoses, mixed emotional frustration, behavior disorders, night enuresis, nervous bulimia, chronic pain syndrome.
Antibiotic with antitumor activity obtained from the Streptomyces caespitosus fungus. It inhibits DNA synthesis, in high concentrations it inhibits the synthesis of protein and RNA. Has a relatively weak immunosuppressive activity.
The drug therapeutic indications include: esophageal cancer, stomach cancer, pancreatic cancer, liver cancer, cancer of the bile ducts, cancer of the colon and rectum, breast cancer, cervical cancer, endometrial cancer, vulvar cancer, non-small cell lung cancer, mesothelioma, cancer of the renal pelvis and ureter, bladder cancer, prostate cancer, malignant tumors of the head and neck, chronic myelocytic leukemia.
It is a combined drug with a fixed solution of dosages of active substances -lisinopril and amlodipine. The first one is a blocker of the enzyme peptidyl. The second hormone activates the discharge of aldosterone by the cortex. ACE restriction leads to reduced absorption of angiotensin.
Since the mechanism is based on the inhibition of the aldosterone and chemosin systems. The pill reduces an arterial pressure in people with high tension as well.
Phenergan is an antiallergic, topical anesthetic, antihistamine, antipruritic, antiemetic, hypnotic, sedative on the basis of Prometnazine.
Female Viagra - women's viagra. Active component Sildenafil citrate, 100 mg which is a part of Women's Viagra at the same time is an active inhibitor of phosphodiesterase (PDE-5) which increases a blood stream to generative organs that promotes blood-impregnation of vulvar lips and the woman's clitoris. In parallel activity of mucous glands increases, providing lubricant in vagina. As a result, a woman gets a natural orgasm and lack of dryness in vagina at sexual intercourse. Drug duration - up to 5 hours. It is necessary to take Female Viagra - women's viagra in a dosage no more than 100 mg (1 tablet) a day and in 30-50 minutes prior to the planned sexual intercourse.
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