Healthcare Archives - Uni Chem

1200px-Cortisol2.svg.png
30/Nov/2020

Overview

Hydrocortisone a naturally occuring corticosteroid used princially for its anti-inflammatory and immunosuppressive actions or as a hormone replacement therapy. Used to reduce swelling and inflammation. Hydrocortisone used in a variety of disorders including allergic conditions, respiratory conditions, blood disorders, digestive problems, eyes, skin, and rheumatic disorders etc.

Primary Characteristics

Hydrocortisone Natural origin and belongs to Steroid. It belongs to Glucocorticoid agonist pharmacological group on the basis of mechanism of action and also classified in Adrenal Cortical Steroids pharmacological group. The Molecular Weight of Hydrocortisone is 362.50.

Its pKa is 13.81.

Indications

Hydrocortisone primarily indicated in conditions like Adrenal insufficiency, Anaphylactic reactions, Apthous ulcers, Atopic eczema, Collagen disease, Congenital adrenal hyperplasia, Contact allergic dermatitis, Discoid eczema, Flexural psoriasis, Graft rejection, Hypercalcaemia, Infantile eczema. Inflammation, Irritant dermatitis, Itching, Joint inflammation, Perineal trauma, Seborrheic dermatitis, Shock, Soft tissue inflammation, Status asthmaticus, Ulcerative protocolitis, and can also given in adjunctive therapy as an alternative drug of choice in Anaphylactic shock, Insect bites and Otitis externa, Sunburn, Ulcerative colitis.

Pharmacokinetics

Oral absorption of Hydrocortisone found to be 100% . Volume of distribution found to be 0.4-0.7 l/kg and plasma protein binding  >90%. Presystemic metabolism noted to be 37% ±37 and metabolism reported extensively via liver. Renal Excretion accounts for major and plasma half life is 6-120 min.

Mechanism of action

The short term effects of corticosteroids are decreased vasodilation and permeability of capillaries, as well as decreased leukocyte migration to sites of inflammation.[A187463] Corticosteroids binding to the glucocorticoid receptor mediates changes in gene expression that lead to multiple downstream effects over hours to days.

Glucocorticoids inhibit neutrophil apoptosis and demargination, inhibit phospholipase A2. which decreases the formation of arachidonic acid derivatives and  inhibit NF-Kappa B and other inflammatory transcription factors, they promote anti-inflammatory genes like interleukin-10.

Lower doses of corticosteroids provide an anti-inflammatory effect, while higher doses immunosuppressive. High doses of glucocorticoids for an extended period bind to the mineralocorticoid receptor, raising sodium levels and decreasing potassium levels.

Side Effects

The severe or irreversible adverse effects of Hydrocortisone, which give rise to further complications include Convulsions. GI bleeding, Telangiectasia, Striae, Glaucoma, Cataract, Pancreatitis. Hypersensitivity reactions, Osteoporosis, Psychosis, Increased intracranial pressure, Growth retardation, Glucose intolerance, Epidermal thinning, Vertebral fractures, Avascular necrosis, Papilloedema, Opthalmic fungal or viral disease, Dendritic corneal ulcers. Thromboembolic disorder, Long bone fractures, Hypokalemic alkalosis, Reduced visual function, Tendon rupture, Intestinal perforation, Opportunistic infections, Addisonian crises, Adrenal atrophy, Increased IOP (intraocular pressure) and Subcutaneous atrophy.

Hydrocortisone produces potentially life-threatening effects which include Anaphylactoid reactions, Addisonian crises, CHF, Opportunistic infections and Acute pancreatitis, GI hemorrhage. which are responsible for the discontinuation of Hydrocortisone therapy.

The signs and symptoms that produced after the acute overdosage of Hydrocortisone include hypomagnesaemia, Adrenal suppression and Hyperkalemia.

The symptomatic adverse reactions produced by Hydrocortisone more or less tolerable and if they become severe. they treated symptomatically, these include Insomnia, Irritation, Allergic reactions, Itching, Burning, Depression, Weight gain, Acne, Euphoria, Menstrual irregularity. Also Perioral dermatitis, Cushingoid facies, Mood swings, Dryness, Local hypopigmentation and Stinging.

Warning / Precautions

Hydrocortisone used with caution in patients with active tuberculosis infection of respiratory tract or in untreated fungal, bacterial or systemic viral infections. Corticosteroids should only be used systemically with great caution in the presence of congestive heart failure (CHF), recent myocardial infraction (MI). Hypertension, diabetes mellitus, epilepsy, glaucoma, hypothyroidism, liver failure, osteoporosis and peptic ulceration or renal impairment. Children may at increase risk of some adverse effects, corticosteroid causes growth retardation and prolonged use rarely justified. Passive immunization recommended to non-immune patients who do come in contact with chickenpox or measles.

Live vaccine not given to patients receiving high dose systemic and corticosteroid therapy nor for atleast 3 months afterwards. killed vaccine or toxoids may be given, although the response may attenuated. During prolong treatment with corticosteroids, patients examined regularly. sodium intake need to be reduced and calcium and potassium supplement may be necessary. Patient should carry cards given full details of their corticosteroid therapy. Avoid and use during pregnancy. Use nasal steroids with caution until healing has occurred. Donot take Hydrocortisone if you allergic to it. Donot exceed recommended dose. Avoid getting this medication in your eyes. Caution required in children.

Storage Conditions

Inj, Oral Susp, Dental Paste, Cream, Oint.

Store Below 40°C. Do not Freeze. Protect from Sunlight.

Suppositories

Store at room temperature, Below 15°C or in refrigerator. Do not Freeze. Protect from Sunlight and Moisture.

Tab

Store at room temperature.

Interference in Pathology

Increases Cortisol metabolites in urine.


Ketoprofen_ball-and-stick-1200x851.png
30/Nov/2020

Overview

Ketoprofen is NSAID (non-steroidal anti-inflammatory drug). Ketoprofen a propionic acid derivative and widely used in the treatment of pateints with rheumatic diseases. It reduces fever, inflammation or swelling and relieves pain. used to treat pain, swelling and stiffness associated with arthritis. also used to treat headaches, muscle aches and dental pain. available for oral, rectal, parentral and topical administration. Chemically Ketoprofen is (R, S)-2-(3-benzoylpheny) propionicacid. It inhibits cyclooxygenase actvity with reduction in the tissue production of prostaglandins such as PGE-2 and PGF-2a.

Primary Characteristics

It is of Synthetic origin and belongs to Propionic Acid. It belongs to Cyclo-oxygenase inhibitor pharmacological group on the basis of mechanism of action and also classified in Analgesics and Anti-inflammatory Agents pharmacological group. The Molecular Weight of Ketoprofn is 254.30.

Its pKa is 4.55.

Indications

Primarily indicated in conditions like Ankylosing spondylitis, Bursitis, Gastro-oesophageal reflux disease, Gout, Lumbago, Management of cushing`s syndrome, Musculoskeletal disorders, Osteoarthritis, Pain, Rheumatic diseases, Rheumatoid and arthritis, Synovitis, Tendinitis, Tenosynovitis, and can also be given in adjunctive therapy as an alternative drug of choice in Dental pain, Dysmenorrhoea, Fever, fever, Infections, Migraine, Orthopedic manipulations.

Pharmacokinetics

Oral absorption of Ketoprofen found to be 94% ±4. Volume of distribution found to be 0.11 l/kg and plasma protien binding is 95%. Presystemic metabolism noted to be 45.5% ±4.5 and metabolism reported extensively by liver. Renal Excretion accounts for 1% (unchanged) and plasma half life is 1.5-4 hr.

Pharmacodynamics

Ketoprofen a nonsteroidal anti-inflammatory agent (NSAIA) with analgesic and antipyretic properties. Pharmacologic actions similar to those of other prototypical NSAIDs, which inhibit prostaglandin synthesis. Ketoprofen used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and alleviate moderate pain.

Mechanism of action

The anti-inflammatory effects of ketoprofen believed to be due to inhibition cylooxygenase-2 (COX-2), an enzyme involved in prostaglandin synthesis via the arachidonic acid pathway. This results in decreased levels of prostaglandins that mediate pain, fever and inflammation. Ketoprofen a non-specific cyclooxygenase inhibitor and inhibition of COX-1 thought to confer some of its side effects, such as GI upset and ulceration. Ketoprofen is thought to have anti-bradykinin activity, as well as lysosomal membrane-stabilizing action. Antipyretic effects may due to action on the hypothalamus, resulting in an increased peripheral blood flow, vasodilation, and subsequent heat dissipation.

Contraindications

Ketoprofen contraindicated in conditions like Peptic ulcer, Bronchospasm and Rhinitis, Renal insufficiency.

Side Effects

The severe or irreversible adverse effects of Ketoprofen, which give rise to further complications include Reduced GFR (glomerular filtration rate), Acute interstitial nephritis and Platelet dysfunction.

Produces potentially life-threatening effects which include Gastrointestinal hemorrhage. which responsible for the discontinuation of Ketoprofen therapy.

The signs and symptoms that produced after the acute overdosage of Ketoprofen include Hypotension, Vomiting, Bronchospasm, Drowsiness, Drowsiness, Abdominal pain and GI hemorrhage.

The symptomatic adverse reactions produced by Ketoprofen more or less tolerable and if they become severe, they can treated symptomatically, these include Vertigo, Nausea, Vomiting, Diarrhea, Constipation, Photosensitivity, Skin rash, Dyspepsia, GI upset, Bullous rash, dyspepsia and Gastric pain.

Warning / Precautions

Ketoprofen used with caution in patients with intrinsic coagulation defects and those on anticoagulant therapy. It should used with caution in patients with compromised cardiac function, hypertension other condition predisposing to fluid retention. It should be used with extra care in the presence of existing controlled infection. Perform periodic auditory (hearing) function and test during chronic therapy. Discontinue drug if skin reaction occurs. Ketoprofen not recommended in the patient who have experienced a severe Aspirin hypersensitivity reactions. IM injection administered cautiouly to patient receiving .



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