Therapeutic Analysis of Topical Corticosteroids & their Combination Products Available in Nigerian Market

There are several topical corticosteroid formulations (including combinations with anti-infectives) that are registered and approved for use in Nigeria. The TCS formulations are listed by their generic names only. Brand details and detailed therapeutic classifications can be found in EMDEX Print or Mobile.

Choosing topical corticosteroids (TCS)

Topical corticosteroids are widely used for a variety of inflammatory skin disorders. They suppress the inflammatory reaction and relieve symptoms, but their actions are not curative and symptoms can recur on discontinuation of therapy.

Safe and effective use of TCS requires careful consideration of the following:

  • Accurate diagnosis.
  • Choice of steroid preparation, relative potency and delivery vehicle.
  • Frequency of application and duration of treatment
  • Potential adverse effects, both local and systemic

Appropriate indications

Topical corticosteroids are generally indicated for symptomatic relief of acute and chronic skin eruptions, where anti-inflammatory, anti-allergenic and antipruritic activity is required.

Indications for TCS include contact dermatitis, eczema (atopic dermatitis), psoriasis, insect bites; symptomatic relief for burning and pruritic lesions, etc. See below for detailed listing of skin conditions that may be responsive to topical steroid therapy.

TCSs should be avoided in untreated tubercular, bacterial and fungal infections involving the skin and in certain viral diseases such as herpes simplex, chickenpox, and vaccinia due to concerns that immunosuppression may exacerbate the infection.

Dosing, frequency of application, and duration of treatment: “The Fingertip Unit Method”

A fingertip is from the very end of the finger to the first crease in the finger. The “Fingertip unit” (FTU) is a validated method of applying topical drugs in suitable safe quantities. One FTU is approximately 0.5 g, and is defined as the amount of topical steroid that can be squeezed out from a tube (with a stand-ard 5 mm nozzle) along an adult’s fingertip i.e., from the very end of the finger to the first crease of an adult’s index finger.

The frequency of application may vary with the product used and the condition being treated. Once or twice-daily application is recommended for most preparations. More frequent application is usually not needed, since the stratum corneum acts as a reservoir for these lipophilic compounds. An alter-nate day or even twice weekly application may be recommended in some chronic conditions due to this depot effect of TCS.

Duration of treatment for most conditions should not exceed 2-4 weeks, regardless of the potency of the TCS. Chronic application of topical steroids can induce tolerance and tachyphylaxis. High-potency steroids should not be used for more than three weeks continuously. If there is worsening of the le-sions or no change noticed, the product needs to be discontinued and re-evaluation of the diagnosis is indicated.

Selecting a vehicle

Topical corticosteroid preparations consist of an active ingredient and a vehicle (or solvent). In addition to being a carrier for the corticosteroid, the vehicle affects potency based on alterations of the steroid release rate and bioavailability.

The selection of vehicle depends on the type of lesions and the anatomical region. Some vehicles should be used only in certain parts of the body. Most topical corticosteroid preparations are available in several forms, including ointments, creams, gels, aerosols and lotions.

Ointments usually contain petrolatum, waxes, paraffin, propylene glycol, or mineral oil.

Preferred vehicle for Palm and Soles; nonhairy skin and also for dry or thick, hyperkeratotic lesions.

Most occlusive, provides better steroid absorption/penetration. Atopic skin conditions due to hydrating nature. Not suitable for hairy and intertriginous areas

Creams (oil-in-water emulsions) have good lubricating qualities and their ability to vanish into the skin make them cosmetically appealing.

May be used in any area of the body. Preferred vehicle for wet or weepy (exudative) lesions due to their drying effect; also for between skin folds.

Good lubricating and vanishing property, and cosmetic appeal. Generally, less potent than ointments. Suitable for use in intertriginous areas unlike ointments

Gels and lotions are the least greasy and occlusive of all topical steroid vehicles.

Gels may be used on the scalp and other hairy skin areas due to their drying & cooling qualities. Jelly-like effect makes it suitable for exudative inflammation (e.g., poison ivy) and for acne. Non-greasy and non-occlusive.

Lotions/Solutions contain alcohol, which has a drying effect on an oozing (weeping) lesion.

Preferred vehicles for the scalp and other hairy skin areas; between skin folds; moist, macerated lesions.

Easy to apply. Non-greasy and non-occlusive. Least potent topical therapies. Drying and cooling effects.

Topical corticosteroids, Combinations with antibacterials and/or antifungals

TCS combination with an anti-infective agent is indicated where the risk of infection is high or where there is an expectation that potentially dangerous numbers of bacteria or fungi will be present on the skin. The use of these combination products should be limited as some of the components can be sensitizing (e.g., Neomycin). These formulations are generally overused and sometimes, for cosmetic reasons. They allow for treatment without proper diagnosis and should be discouraged.

Recommendations for optimizing the use of topical corticosteroids

  • Children generally require a shorter duration of treatment and a lower potency steroid.
  • Prescribe for the right dermatoses, not as empiric therapy for every “rash”.
  • Use appropriate steroid formulation and potency to achieve disease control.
  • Initiate maintenance therapy with a lower potency steroid after achieving control of the acute inflammation.
  • Taper off the treatment upon complete remission of skin diseases, after prolonged therapy.
  • Limit the duration of use
  • Caution when prescribing topical steroid for certain body regions (e.g., groin, face, axillae, and flexures).
  • To be aware of the adverse effects and act immediately to counteract them.
  • When infections necessitate the addition of an antibiotic or antifungal, systemic treatment should be considered.
  • When the diagnosis is unclear or the condition is nonresponsive to standard treatment, refer to a dermatologist.

Comparison of topical corticosteroids

Ultra-high and High Potency TCS

Recommended for thick skin areas like Palm and Soles for: Atopic dermatitis (resistant); Discoid lupus; Hyperkeratotic eczema; Lichen planus; Lichen sclerosus (skin); Psoriasis; Severe hand eczema.

High-potency may also be used on the Trunk, Extremities, Scalp & Hairy skin areas for: Scalp dermatitis; Atopic dermatitis; Psoriasis, etc.

They pose the highest risk of systemic side effects. Avoid abrupt discontinuation; continuous daily use >3 weeks, and occlusive dressings.

Monitor for symptoms of adrenal suppression: weakness, weight loss, hypotension, and gastrointestinal distress.

Lower potency agents are preferred for the face, groin, armpits, or skin folds due to susceptibility to local side effects and systemic absorption

Ultra-high potency includes: Betamethasone dipropionate glycol (augmented) 0.05% Cream, Ointment, Lotion; Clobetasol 17-propionate 0.05% Cream, Ointment, Lotion; Halobetasol propionate 0.05% Ointment.

High potency includes: Amcinonide 0.1% Ointment, Cream, Lotion; Betamethasone dipropionate 0.05% Ointment, Cream, Lotion; Betamethasone valerate 0.1% Ointment; Fluocinonide 0.05% Cream, Ointment, Gel; Halobetasol propionate 0.05% Cream; Mometasone furoate 0.1% Ointment.

Moderate Potency TCS

Recommended for Trunk, Extremities, Scalp & Hairy skin areas for: Alopecia areata; Atopic dermatitis; Contact dermatitis (severe); Lichen sclerosus (vulva); Nummular eczema; Perianal inflammation (severe); Scabies (after scabicide); Seborrheic dermatitis; Severe dermatitis; Severe intertrigo (short-term); Stasis dermatitis.

Moderate to low potency agents should be used when treatment involves large body surface area.

Duration of treatment: May be used for up to 3 months when treating non-facial or non-intertriginous areas.

Occlusive dressings should be avoided.

Low Potency TCS

Recommended for thin skin areas like Face, Neck, Intertriginous or Genital areas for: Dermatitis (face, eyelids, diaper region); Intertrigo; Perianal inflammation.

These are agents of choice for children, pregnant women, elderly or for treating large areas.

Available TCS Combinations with Antibiotics

  • Betamethasone + Neomycin (Topical)
  • Hydrocortisone + Gentamicin (Topical)
  • Hydrocortisone + Neomycin (Topical)

Available TCS Combinations with Antifungals

  • Beclometasone + Clotrimazole
  • Betamethasone + Clotrimazole
  • Clobetasol + Clotrimazole
  • Dexamethasone + Clotrimazole
  • Diflucortolone + Isoconazole
  • Hydrocortisone + Miconazole (Topical)

Available TCS Combinations with Antibiotics and Antifungals

  • Beclometasone + Clotrimazole + Gentamicin
  • Beclometasone + Clotrimazole + Gentamicin + Clioquinol
  • Betamethasone + Clotrimazole + Gentamicin
  • Betamethasone + Clotrimazole + Neomycin
  • Betamethasone + Tolnaftate + Gentamicin
  • Betamethasone + Tolnaftate + Gentamicin + Clioquinol
  • Betamethasone + Tolnaftate + Neomycin + Clioquinol
  • Clobetasol + Ketoconazole + Neomycin
  • Clobetasol + Miconazole + Gentamicin
  • Clobetasone + Miconazole + Gentamicin
  • Dexamethasone + Clotrimazole + Gentamicin
  • Dexamethasone + Clotrimazole + Neomycin
  • Dexamethasone + Miconazole + Neomycin
  • Fluocinolone + Miconazole + Neomycin
  • Miconazole + Beclometasone + Neomycin
  • Miconazole + Clobetasol + Neomycin
  • Triamcinolone + Econazole + Gentamicin

Adverse effects of topical corticosteroids (TCS)

Risk factors for adverse effects

  • Duration of treatment — long-term treatment is likely to result in systemic absorption.
  • Area of the skin being treated — treating large areas of skin increases the risk of absorption.
  • Condition of the skin — absorption is greatest in thin, inflamed skin.
  • Potency of the topical corticosteroid — the greater the potency, the greater the risk of absorption.
  • Occlusion — use of topical corticosteroids under occlusion increases the risk of systemic absorption.
  • Age — children and elderly people are more susceptible to the adverse effects of topical corticosteroids because they have a thinner epidermis.

Local adverse effects

Common and mostly occur on the face, in skin folds, and in areas that are treated over the long term

  • Transient burning or stinging — this is common, especially in the first 2 days of application on untreated, inflamed skin.
  • Worsening and spreading of untreated infection.
  • Thinning of the skin (atrophy) — the skin improves over a period after stopping treatment.
  • Permanent stretch marks or striae. Most common in the groin, axillae, and inner thigh areas.
  • Allergic contact dermatitis — due to the corticosteroid or the excipients. Lower potency agents like Hydrocortisone may be more allergenic.
  • Acne (or worsening of existing acne) or rosacea. Common in the face with high potency agents.
  • Hypopigmentation — More common in the blacks. May be reversible.
  • Excessive hair growth at the site of application (hypertrichosis). Reversible.

Systemic adverse effects

Rare, but may occur more frequently in the presence of risk factors including infants and children

  • Adrenal suppression.
  • Cushing’s syndrome.
  • Hyperglycaemia
  • Growth retardation in children.

Minimizing adverse effects

  • Prescribe the least potent formulation which is fully effective (advise the person to apply it thinly to affected areas, no more than twice daily).
  • Consider prescribing an appropriate quantity of an emollient for use alongside the topical corticosteroid (for moisturizing purposes).
  • Avoid prescribing potent corticosteroids for use on the face.
  • Unless under specialist supervision, the use of potent (such as betamethasone valerate 0.1%) and very potent (such as clobetasol propionate 0.1%) topical corticosteroids, should be limited to: Use for up to 2 weeks, and No more than 50 g each week; Once–daily application is usually sufficient — maximum of twice daily.
  • Avoid using occlusive dressings with topical corticosteroids (especially on large areas of the body).
  • If a topical corticosteroid is needed for maintenance therapy, consider incorporating regular periods when they are withdrawn (for as long as possible) and emollients are used on their own.
  • If the person is using large amounts of topical corticosteroid regularly, monitor them for signs of systemic adverse effects (such as adrenal suppression) and local adverse effects (such as areas of thin skin or striae).
  • Monitor the height of children who are using large amounts of topical corticosteroid.

References

Available on request

Therapeutic Analysis of Cough & Cold Preparations Available in Nigerian Market

Flu, COVID-19, Allergies, or a Cold?

Specific treatment recommendations for the common symptoms associated with cough and cold

Productive cough:

Characterized by the presence of excessive sputum and may be associated with various underlying diseases e.g. chronic bronchitis, Tuberculosis, LVF etc.

Treatment of the underlying cause recommended e.g. with antibiotics.

Avoid antitussives as suppression of cough can be harmful

Expectorants may help to reduce sputum viscosity so bronchial secretions can be expectorated. There are 2 types:

  • Mucolytic expectorants e.g. Ambroxol, Acetylcysteine, Carbocysteine, Bromhexine.
  • Mucokinetic expectorants e.g. Sodium or potassium citrate, Ammonium chloride, Potassium iodide, Guaifenesin, Tolu balsam.

Expectorants may cause bronchospasm in patients with asthma.

Non-productive cough:

Characterized by dry, irritating cough with little or no sputum.

Suppression of cough using antitussives (e.g. Dextromethorphan, Codeine) usually indicated

May cause excessive drowsiness

Postnasal drip cough:

A combination of first-generation antihistamine (e.g. diphenhydramine, chlorphenamine) and nasal decongestant (e.g. pseudoephedrine, phenylephrine) may be indicated. Antibiotics may be added if necessary for bacterial sinusitis.

Caution when using decongestants in patients with hypertension or other cardiovascular disease.

Asthmatic cough:

Short-acting beta-agonists (SABAs e.g. Salbutamol, Terbutaline) are usually indicated. Inhaled corticosteroids may be added depending on the severity.

GERD-associated cough:

H2RA (e.g. Ranitidine, Famotidine) or PPI (e.g. Omeprazole, Pantoprazole) are the treatments of choice. Non-drug measures include elevation bedhead, light dinner, diet modification, etc.

ACE inhibitor associated cough:

Substitute ACEI with ARB (e.g. Losartan). Antitussives not useful

Nasal congestion:

Systemic decongestants (e.g. Pseudoephedrine, Phenylephrine) or nasal decongestants (e.g. Oxymetazoline, Xylometazoline) may be useful.

They act indirectly to reduce blood flow, edema and swelling in the nasal area, thereby helping to alleviate nasal congestion.

Side effects may include rebound congestion, palpitations, tachycardia, burning sensation with topical agents.

Caution in patients with cardiovascular disease especially with the systemic agents.

Saline spray or drops may be effective alternatives and should be considered first-line especially in children.

Sneezing, rhinorrhea:

First-generation antihistamines (e.g. Chlorphenamine, Diphenhydramine) can be useful in controlling runny nose due to their anticholinergic properties. Non-drowsy antihistamines (e.g. Loratadine) are also effective especially when allergy is the underlying cause

Fever, headache, sore throat:

Analgesics (e.g. Paracetamol, Ibuprofen) are generally useful.

Non-drug measures namely increased fluid intake and rest can be beneficial in most cases of cough and cold.

Therapeutic classification of compound cough & cold preparations available in Nigeria

See EMDEX Mobile App for the proprietary preparations

Analgesic-containing preparations

Analgesic with Antihistamine

  • Paracetamol + Cetirizine
  • Paracetamol + Chlorphenamine
  • Paracetamol + Diphenhydramine

Analgesic with Antihistamine & Antitussive

  • Paracetamol + Loratadine + Dextromethorphan
  • Paracetamol + Doxylamine + Dextromethorphan

Analgesic with Antihistamine & Expectorant

  • Paracetamol + Chlorphenamine + Ammonium chloride + Sodium citrate

Analgesic with Antihistamine & Vitamin C

  • Paracetamol + Chlorphenamine + Ascorbic acid

Analgesic with Decongestant & Antihistamine

  • Paracetamol + Phenylephrine + Chlorphenamine
  • Paracetamol + Caffeine + Phenylephrine + Chlorphenamine
  • Paracetamol + Caffeine + Phenylephrine + Pheniramine
  • Paracetamol + Pseudoephedrine + Chlorphenamine
  • Paracetamol + Caffeine + Pseudoephedrine + Chlorphenamine
  • Paracetamol + Pseudoephedrine + Triprolidine

Analgesic with Decongestant & Antitussive

  • Paracetamol + Phenylephrine + Dextromethorphan
  • Paracetamol + Pseudoephedrine + Dextromethorphan

Analgesic with Decongestant, Antihistamine & Vitamin C

  • Paracetamol + Caffeine + Phenylephrine + Chlorphenamine + Ascorbic acid

Analgesic with Decongestant, Antihistamine & Expectorant

  • Paracetamol + Pseudoephedrine + Chlorphenamine + Ammonium chloride

Analgesic with Decongestant, Antihistamine & Antitussive

  • Paracetamol + Pseudoephedrine + Chlorphenamine + Dextromethorphan

Compound decongestant preparations

See analgesic-containing preparations above.

Decongestant with Antihistamine

  • Phenylephrine + Chlorphenamine
  • Pseudoephedrine + Chlorphenamine

Decongestant with Antihistamine & Antitussive

  • Pseudoephedrine + Chlorphenamine + Dextromethorphan
  • Phenylephrine + Chlorphenamine + Dextromethorphan
  • Ephedrine + Promethazine + Codeine

Decongestant with Antihistamine & Expectorant

  • Ephedrine + Chlorphenamine + Ammonium chloride + Sodium citrate + Menthol
  • Ephedrine + Diphenhydramine + Ammonium chloride + Sodium citrate + Menthol
  • Ephedrine + Cetirizine + Ammonium chloride + Sodium citrate
  • Ephedrine + Cetirizine + Ammonium chloride + Sodium citrate + Menthol
  • Ephedrine + Chlorphenamine + Ammonium chloride + Sodium citrate

Decongestant with Antihistamine, Antitussive & Expectorant

  • Phenylephrine + Chlorphenamine + Dextromethorphan + Guaifenesin
  • Pseudoephedrine + Triprolidine + Codeine + Potassium guaiacolsulfonate

Compound antihistamine preparations

See analgesic- and decongestant-containing preparations above

Antihistamine with Expectorant

  • Diphenhydramine + Ammonium chloride + Ammonium bicarbonate
  • Diphenhydramine + Ammonium chloride
  • Diphenhydramine + Sodium citrate
  • Chlorphenamine + Ammonium chloride + Sodium citrate
  • Chlorpheniramine + Ammonium chloride + Sodium citrate + Guaifenesin
  • Chlorphenamine + Ammonium chloride + Sodium citrate + Ipecacuanha
  • Chlorphenamine + Ammonium chloride + Sodium citrate + Ipecacuanha + Menthol
  • Diphenhydramine + Ammonium chloride + Sodium citrate + Menthol
  • Diphenhydramine + Ammonium chloride + Menthol
  • Diphenhydramine + Sodium citrate + Menthol
  • Diphenhydramine + Sodium citrate + Menthol + Tolu
  • Chlorphenamine + Ammonium chloride + Sodium citrate + Menthol
  • Chlorphenamine + Sodium citrate + Menthol

Antihistamine with Antitussive

  • Chlorphenamine + Dextromethorphan
  • Promethazine + Pholcodeine

Antihistamine with Antitussive & Expectorant

  • Chlorphenamine + Dextromethorphan + Guaifenesin
  • Diphenhydramine + Codeine + Sodium citrate + Menthol
  • Diphenhydramine + Codeine + Ammonium chloride + Sodium citrate + Menthol
  • Diphenhydramine + Codeine + Ammonium chloride + Menthol

Antihistamine with Menthol

  • Diphenhydramine + Menthol
  • Cetirizine + Menthol

Compound mucolytic/expectorant preparations

See also above for preparations containing analgesic, decongestant or antihistamine

Antitussive with Expectorant

  • Dextromethorphan + Guaifenesin

Expectorants with Demulcents

  • Thyme + Primula
  • Squill oxymel + Ipecacuanha
  • Ammonium chloride + Ipecacuanha + Liquorice
  • Ammonium chloride + Ipecacuanha + Liquorice + Peppermint oil
  • Ipecacuanha + Honey + Glycerol
  • Ammonium chloride + Sodium citrate + Squill + Menthol
  • Sodium citrate + Ipecacuanha + Squill oxymel + Anise water + Menthol
  • Ipecacuanha + Citric acid + Honey + Glycerol

Mucolytic with Antibiotic

  • Bromhexine + Co-trimoxazole

Mucolytic with Antihistamine

  • Carbocisteine + Promethazine

Mucolytic with Antihistamine & Expectorant

  • Bromhexine + Diphenhydramine + Ammonium chloride + Menthol

Mucolytic with Antitussive & Expectorant

  • Bromhexine + Dextromethorphan + Ammonium chloride + Menthol

Mucolytic with Expectorant & Bronchodilator

  • Bromhexine + Guaifenesin + Salbutamol
  • Bromhexine + Guaifenesin + Salbutamol + Menthol
  • Bromhexine + Guaifenesin + Terbutaline + Menthol
  • Ambroxol + Guaifenesin + Salbutamol + Menthol

Other compound cough & cold mixtures

Herbal cough & cold remedies

  • Thyme + Grindelia + Pimpinella + Primrose + Rose

Glycrrhiza + Terminalia + Zingiber + Curcuma + Mentha

India bans 328 fixed-dose combination drugs

Some of these drug products are available in Nigeria

The government of India has banned the manufacture, sale and distribution of 328 combination drugs with immediate effect, describing them as “irrational” and “unsafe” drug combinations. See the A-Z list below.

According to the health ministry, there was “no therapeutic justification for the ingredients contained in the 328 FDCs and that these FDCs may involve risk to human beings”.

The All India Drug Action Network welcomed the government ban, saying “The people of India have been made the consumers of unsafe medicines for too long,”.

The president of the Indian Drug Manufacturers’ Association said the verdict would be respected

(Source: Reuters and Times of India)

List of 328 combination drugs banned by India – September 13, 2018

  • Aceclofenac (SR) + Paracetamol
  • Aceclofenac + Paracetamol + Famotidine
  • Aceclofenac + Paracetamol + Rabeprazole
  • Aceclofenac + Zinc Carnosine
  • Acetaminophen + Guaifenesin + Dextromethorphan + Chlorpheniramine
  • Acetaminophen + Loratadine + Ambroxol + Phenylephrine
  • Acriflavine + Thymol + Cetrimide
  • Acrivastine + Paracetamol + Caffeine + Phenylephrine
  • Albuterol + Bromhexine + Theophylline
  • Albuterol + Etofylline + Bromhexine + Menthol
  • Alginic Acid + Sodium Bicarbonate + Dried Aluminium Hydroxide + Magnesium Hydroxide
  • Allantoin + Dimethicone + Urea + Propylene + Glycerin + Liquid Paraffin
  • Ambroxol + Levocetirizine + Phenylephrine + Guaiphenesin + Menthol
  • Ambroxol + Guaifenesin + Phenylephrine + Chlorpheniramine
  • Ambroxol + Salbutamol + Choline Theophyllinate + Menthol
  • Ambroxol + Salbutamol + Theophylline
  • Ambroxol + Terbutaline + Dextromethorphan
  • Ambroxol+ Guaiphenesin + Ammonium Chloride + Phenylephrine + Chlorpheniramine Maleate + Menthol
  • Ammonium Chloride + Dextromethorphan + Cetirizine + Menthol
  • Ammonium Chloride + Sodium Citrate + Chlorpheniramine Maleate + Menthol
  • Ammonium Citrate + Vitamin B 12 + Folic Acid + Zinc Sulphate
  • Amoxicillin + Cefixime + Potassium Clavulanic Acid
  • Amoxicillin + Dicloxacillin
  • Amoxicillin 250 mg + Potassium Clavulanate Diluted 62.5
  • Amoxycillin + Dicloxacillin + Serratiopeptidase
  • A moxycillin + Tinidazole
  • Ascorbic Acid + Manadione Sodium Bisulphate + Rutin + Dibasic Calcium Phosphate + Adrenochrome mono Se
  • Atorvastatin + Vitamin D3 + Folic Acid + Vitamin B12 + Pyridoxine
  • Azithromycin + Acebrophylline
  • Azithromycin + Ambroxol
  • Azithromycin + Cefixime
  • Azithromycin + Cefpodoxime
  • Azithromycin + Levofloxacin
  • Azithromycin + Ofloxacin
  • Beclomethasone + Clotrimazole + Chloramphenicol + Gentamycin + Lignocaine Ear drops
  • Beclomethasone + Clotimazole + Neomycin + lodochlorohydroxyquinone
  • Beclomethasone + Clotrimazole + Gentamicin + lodochlorhydroxyquinoline
  • Beclomethasone Diproprionate + Neomycin + Tolnaftate + lodochlorhydroxyquinoline + Chlorocresol
  • Benfotiamine + Metformin
  • Benzoxonium Chloride + Lidocaine
  • Betahistine + Ginkgo Biloba Extract + Vinpocetine + Piracetam
  • Betamethasone + Fusidic Acid + Gentamycin + Tolnaftate + lodochlorhydroxyquinoline (ICHQ)
  • Betamethasone + Gentamicin + Tolnaftate + lodochlorhydroxyquinoline
  • Betamethasone + Gentamycin + Zinc Sulphate + Clotrimoazole + Chlorocresol
  • Betamethasone + Neomycin + Tolnaftate + lodochlorohydroxyquinoline + Cholorocresol
  • Borax + Boric Acid + Naphazoline + Menthol + Camphor + Methyl Hydroxy Benzoate
  • Bromhexine + Phenylephrine + Chlorpheniramine + Paracetamol
  • Bromhexine + Cetirizine + Phenylephrine IP+Guaifenesin + Menthol
  • Bromhexine + Dextromethorphan
  • Bromhexine + Dextromethorphan + Phenylephrine + Menthol
  • Bromhexine + Phenylephrine + Chlorepheniramine Maleate
  • Caffeine + Paracetamol + Chlorpheniramine
  • Caffeine + Paracetamol + Phenylephrine + Cetirizine
  • Calcium Gluconate + Chlorpheniramine + Vitamin C
  • Calcium Gluconate + Levocetirizine
  • Cefixime + Levofloxacin
  • Cefixime + Linezolid
  • Cefpodoxime Proxetil + Levofloxacin
  • Cefuroxime + Linezolid
  • Cephalexin + Neomycin + Prednisolone
  • Certirizine + Phenylephrine + Paracetamol + Caffeine + Nimesulide
  • Cetirizine + Acetaminophen + Dextromethorphan + Phenyephrine + Zinc Gluconate
  • Cetirizine + Ambroxol + Guaiphenesin + Ammonium Chloride + Phenylephrine + Menthol
  • Cetirizine + Dextromethorphan + Ambroxol
  • Cetirizine + Dextromethorphan + Bromhexine + Guaifenesin
  • Cetirizine + Dextromethorphan + Phenylephrine + Tulsi
  • Cetirizine + Dextromethorphan + Phenylephrine + Zinc Gluconate + Paracetamol + Menthol
  • Cetirizine + Dextromethorphan + Zinc Gluconate + Menthol
  • Cetirizine + Diethylcarbamazine
  • Cetirizine + Phenylephrine + Dextromethorphan + Menthol
  • Cetirizine + Phenylephrine + Paracetamol + Ambroxol + Caffeine
  • Cetirizine + Phenylephrine + Paracetamol + Zinc Gluconate
  • Cetririzine + Nimesulide + Phenylephrine
  • Chlopheniramine Maleate + Dextromethorphan + Guaiphensin + Phenylephrine
  • Chloramphenicol + Beclomethasone + Clomitrimazole + Lignocaine
  • Chloramphennicol + Lignocaine + Betamethasone + Clotrimazole + Ofloxacin + Antipyrine
  • Chlorphaniramine + Ammonium Chloride + Sodium Chloride
  • Chlorpheniramine + Ammonium Chloride + Chloroform + Menthol
  • Chlorpheniramine + Ammonium Chloride + Noscapine + Sodium Citrate
  • Chlorpheniramine + Codeine + Sodium Citrate + Menthol Syrup
  • Chlorpheniramine + Dextromethorphan + Phenylephrine + Paracetamol
  • Chlorpheniramine + Paracetamol + Pseudoephedrine + Caffeine
  • Chlorpheniramine + Phenylephrine + Caffeine
  • Chlorpheniramine + Phenylephrine + Dextromethophan + Menthol
  • Chlorpheniramine + Phenylephrine + Paracetamol + Zink Gluconate
  • Chlorpheniramine + Terpin + Antimony Potassium Tartrate + Ammonium Chloride + Sodium Citrate + Menthol
  • Chlorpheniramine + Vasaka + Tolubalsm + Ammonium Chloride + Sodium Citrate + Menthol
  • Chlorpheniramine + Vitamin C
  • Chlorpheniramine Maleate + Ammonium Chloride + Sodium Citrate
  • Chlorpheniramine + Ammonium Chloride + Menthol
  • Chlorpromazine + Trihexyphenidyl
  • Chromium Polynicotinate + Metformin
  • Cilnidipine + Metoprolol Succinate + Metoprolol Tartrate
  • Ciprofloxacin + Fluocinolone + Clotrimazole + Neomycin + Chlorocresol
  • Ciprofloxacin + Fluticasone + Clotrimazole + Neomycin
  • Ciprofloxacin + Phenazopyridine
  • Clidinium + Paracetamol + Dicyclomine + Activated Dimethicone
  • Clindamycin + Clotrimazole + Lactic Acid Bacillus
  • Clindamycin + Telmisartan
  • Clobetasol + Gentamicin + Tolnaftate + lodochlorhydroxyquinone + Ketoconazole
  • Clobetasol + Neomycin + Miconazole + Clotrimazole
  • Clobetasol + Neomycin + Miconazole + Zinc Sulphate
  • Clobetasol + Ofloxacin + Ketoconazol + Zinc Sulphate
  • Clobetasol + Ofloxacin + Miconazole + Zinc Sulphate
  • Clobetasol Propionate + Ofloxacin + Ornidazole + Terbinafine
  • Clobetasole + Gentamicin + Miconazole + Zinc Sulphate
  • Clomifene Citrate + Ubidecarenone + Zinc + Folic Acid + Methylcobalamin + Pyridoxine + Lycopene + Selenium + Levocarnitine Tartrate + L-Arginine
  • Clotrimazole + Beclomethasone + Lignocaine + Ofloxacin + Acetic Aicd + Sodium Methyl Paraben + Propyl Paraben
  • Clotrimazole + Beclomethasone + Ofloxacin + Lignocaine
  • Clotrimazole + Ofloxaxin + Lignocaine + Glycerine and Propylene Glycol
  • Codeine + Chlorpheniramine + Alcohol Syrup
  • Codeine + Levocetirizine + Menthol
  • Combikit of 3 tablets of Serratiopeptidase (enteric c oated 20000 units) + Diclofenac Potassium & 2 tablets of D
  • Combikit of Azithromycin, Secnidazole and Fluconazole
  • Combikit of Fluconazole Tablet, Azithromycin Tablet and Ornidazole Tablets
  • Cyproheptadine + Thiamine
  • Dextrometharphan + Chlopheniramine + Ammonium Chloride+ Menthol
  • Dextrometharphan + Chlopheniramine + Ammonium + Sodium Citrate + Menthol
  • Dextrometharphan + Phenylephrine + Guaiphenesin
  • Dextromethophan + Chlopheniramine + Bromhexine
  • Dextromethorphan + Ambroxol + Ammonium Chloride + Chlorpheniramine + Menthol
  • Dextromethorphan + Ambroxol + Guaifenesin + Phenylephrine + Chlorpheniramine
  • Dextromethorphan + Bromhexine + Guaiphenesin
  • Dextromethorphan + Bromhexine + Guaiphenesin + Menthol
  • Dextromethorphan + Cetirizine
  • Dextromethorphan + Cetirizine + Guaifenesin + Ammonium Chloride
  • Dextromethorphan + Chlorpheniramine + Chlorpheniramine Maleate
  • Dextromethorphan + Chlorpheniramine + Guaiphenesin
  • Dextromethorphan + Levocetirizine + Phenylephrine + Zinc
  • Dextromethorphan + Paracetamol + Cetirizine + Phenylephrine
  • Dextromethorphan + Phenylephrine + Ammonium Chloride + Menthol
  • Dextromethorphan + Phenylephrine + Bromhexine + Guaifenesin + Chlorpheniramine
  • Dextromethorphan + Phenylephrine + Cetirizine + Paracetamol + Caffeine
  • Dextromethorphan + Phenylephrine + Cetirizine + Zinc + Menthol
  • Dextromethorphan + Phenylephrine + Guaifenesin + Certirizine + Acetaminophen
  • Dextromethorphan + Phenylephrine + Guaifenesin + Triprolidine
  • Dextromethorphan + Phenylephrine + Tripolidine + Menthol
  • Dextromethorphan + Phenylephrine + Zinc Gluconate + Menthol
  • Dextromethorphan + Tripolidine + Phenylephirine
  • Dextromethorphan + Triprolidine + Phenylephrine
  • Dextromethorphan + Bromhexine + Chlorpheniramine Maleate + Guaiphenesin
  • Dextromethorphan + Promethazine
  • Diclofenac + Paracetamol + Chlorpheniramine maleate + Magnesium Trisillicate
  • Diclofenac + Paracetamol + Chlorzoxazone + Famotidine
  • Diclofenac + paracetamol + Magnesium Trisilicate
  • Diclofenac + Paracetamol injection
  • Diclofenac + Tramadol + Chlorzoxazone
  • Diclofenac + Tramadol + Paracetamol
  • Diclofenac + Zinc Carnosine
  • Dicyclomine + Paracetamol + Domperidone
  • Diethyl Carbamazine + Chlorpheniramine + Guaifenesin
  • Diethylcabamazine Citrate + Cetirizine + Guaiphenesin
  • Diethylcarbamazine + Cetirizine + Ambroxol
  • Diphenhydramine + Guaifenesin + Bromhexine + Ammonium Chloride + Menthol
  • Diphenhydramine + Guaiphenesin + Ammonium Chloride + Bromhexine
  • Diphenhydramine + Terpine + Ammonium Chloride + Sodium Chloride + Menthol
  • Diphenoxylate + Atropine + Furazolidonee
  • Disodium Hydrogen Citrate + Paracetamol
  • Doxycycline + Serratiopeptidase
  • Doxylamine + Pyridoxine + Mefenamic Acid + Paracetamol
  • Dried Alumnium Hydroxie Gel + Prophantheline + Diazepam
  • Drotaverine + Clidinium + Chlordiazepoxide
  • Enrofloxacin + Bromhexin
  • Ergotamine Tartrate + Belladona Dry Extarct+Caffeine + Paracetamol
  • Ethylmorphine + Noscapine + Chlorpheniramine
  • Famotidine + Oxytacaine + Magaldrate
  • Flunarizine + Paracetamole + Domperidone
  • Flupentixol + Escitalopram
  • Furazolidone + Metronidazole + Loperamide
  • Gabapentin + Mecobalamin + Pyridoxine + Thiamine
  • Gentamicin Sulphate + Clotrimazole + Betamethasone + Lignocaine
  • Gentamycin + Dexamethasone + Chloramphenicol + Tobramycin + Ofloxacin
  • Glibenclamide + Metformin (SR)+ Pioglitazone
  • Gliclazide 40mg + Metformin 400mg
  • Gliclazide 80 mg + Metformin 325 mg
  • Glimepiride + Pioglitazone + Metformin
  • Glimepiride 1mg/2mg/3mg + Pioglitazone 15mg/15mg/15mg + Metformin 1000mg/1000mg/1000mg
  • Glimepiride 1mg/2mg+ Pioglitazone 15mg/15mg + Metformin 850mg/850mg
  • Glipizide 2.5mg + Metformin 400 mg
  • Glucosamine + Methyl Sullfonyl Methane + Vitamin D3 + Manganese + Boron + Copper + Zinc
  • Guaifenesin + Bromhexine + Chlorpheniramine + Paracetamol
  • Guaifenesin + Bromhexine + Chlorpheniramine + Phenylephrine + Paracetamol + Serratiopeptidase (as enteric coated granules) 10000 SP Units
  • Guaifenesin + Dextromethorphan
  • Guaifenesin + Diphenhydramine + Bromhexine + Phenylephrine
  • Heparin + Diclofenac
  • Imipramine + Chlordiazepoxide + Trifluoperazine + Trihexyphenidyl
  • Ketoconazole + Tea Tree oil + Allantion + Zinc Oxide + Aloe Vera + Jojoba oil + Lavander oil + Soa noodels
  • Ketotifen + Cetirizine
  • Ketotifen + Levocetrizine
  • Ketotifen + Theophylline
  • L-5-Methyltetrahydrofolate Calcium + Escitalopram
  • L-Arginine + Sildenafil
  • Levocetirizine + Ambroxol + Phenylephrine + Guaiphenesin
  • Levocetirizine + Ambroxol + Phenylephrine + Paracetamol
  • Levocetirizine + Dextromethorphan + Zinc
  • Levocetirizine + Montelukast + Acebrophylline
  • Levocetirizine + Paracetamol + Phenylephirine + Caffeine
  • Levocetirizine + Phenylephrine + Ambroxol + Guaiphenesin + Paracetamol
  • Levocetirizine + Ranitidine
  • Levofloxacin + Bromhexine
  • Levofloxacin + Ornidazole + Alpha Tocopherol Acetate
  • Levothyroxine + Phyridoxine + Nicotinamide
  • Lignocaine + Clotrimazole + Ofloxacin + Beclomethasone
  • Lornoxicam + Paracetamol + serratiopeptidase
  • Lornoxicam + paracetamol + Tramadol
  • Lornoxicam + paracetamol + trypsin
  • Magaldrate + Famotidine + Simethicone
  • Magaldrate + Papain + Fungul Diastase + Simethicone
  • Magaldrate + Ranitidine + Pancreatin + Domperidone
  • Mebeverine & Inner HPMC capsule (Streptococcus Faecalis + Clostridium butyricum + Bacillus mesentricus + Lactic Acid Bacillus)
  • Menthol + Anesthetic Ether
  • Metformin (SR) 500mg + Pioglitazone 5mg
  • Metformin (Sustainded Release) 500mg + Pioglitazone 15 mg + Glimepiride 3mg
  • Metformin + Atorvastatin
  • Metformin + Bromocriptine
  • Metformin + Gliclazide + Chromium Polynicotinate
  • Metformin + Gliclazide + Piogllitazone + Chromium Polynicotinate
  • Metformin + Glimepiride + Methylcobalamin
  • Metformin 1000/1000/500/500mg + Pioglitazone 7.5/7.5/7.5/7.5mg + Glimepiride 1/2/1/2mg
  • Metformin 500mg/500mg+Gliclazide SR 30mg/60mg + Pioglitazone 7.5mg/7.5mg
  • Metformin 850mg + Pioglitazone 7.5 mg + Glimepiride 1mg
  • Metformin 850mg + Pioglitazone 7.5 mg + Glimepiride 2mg
  • Metformin ER + Gliclazide MR + Voglibose
  • Metronidazole + Norfloxacin
  • Metronidazole + Tetracycline
  • N-Acetyl Cysteine + Ambroxol + Phenylephrine + Levocertirizine
  • Naphazoline + Carboxy Methyl Cellulose + Menthol + Camphor + Phenylephrine
  • Naphazoline + Chlorpheniramine + Zinc Sulphate + Boric Acid + Sodium Chloride + Chlorobutol
  • Naproxen + Paracetamol
  • Neomycin + Doxycycline
  • Nimesulide + Certirizine + Phenylephrine
  • Nimesulide + Cetrizine + Caffeine
  • Nimesulide + Diclofenac
  • Nimesulide + Dicyclomine
  • Nimesulide + Loratadine + Phenylephrine + Ambroxol
  • Nimesulide + Paracetamol + Cetirizine + Phenylephrine
  • Nimesulide + Paracetamol + Levocetirizine + Phenylephrine + Caffeine
  • Nimesulide + Paracetamol Injection
  • Nimesulide + Paracetamol Suspension
  • Nimesulide + Phenylephrine + Caffeine + Levocetirizine
  • Nimesulide + Pitofenone + Fenpiverinium + Benzyl Alcohol
  • Nimesulide + Serratiopeptidase
  • Nimesulide + Tizanidine
  • Nimorazole + Ofloxacin
  • Norfloxacin+ Metronidazole + Zinc Acetate
  • Oflaxacin + Ornidazole Suspension
  • Ofloxacin + Clotrimazole + Betamethasone + Lignocaine
  • Ofloxacin + Metronidazole + Zinc Acetate
  • Ofloxacin + Nitazoxanide
  • Ofloxacin + Ornidazole + Zinc Bisglycinate
  • Olmesartan + Hydrochlorothiazide + Chlorthalidone
  • Omepraozle + Paracetmaol+ Diclofenac
  • Oxetacaine + Magaldrate + Famotidine
  • Pantoprazole (as Enteric Coated Tablet) + Zinc Carnosine (as Film Coated Tablets
  • Paracetamol + Ambroxol + Phenylephrine + Chlorpheniramine
  • Paracetamol + Caffeine + Codeine
  • Paracetamol + Caffine + Phenylephrine + Chlorpheniramine
  • Paracetamol + Cetrizine + Caffeine
  • Paracetamol + Chlorpheniramine + Ambroxol + Guaifenesin + Phenylephrine
  • Paracetamol + Codeine + Chlorpheniramine
  • Paracetamol + Dextromethorphan + Bromhexine + Phenylephrine + Diphenhydramine
  • Paracetamol + Dextromethorphan + Chlorpheniramine
  • Paracetamol + Diclofenac + famotidine
  • Paracetamol + Disodium Hydrogen Citrate + Caffeine
  • Paracetamol + DL Methionine
  • Paracetamol + domperidone + Caffeine
  • Paracetamol + Levocetirizine + Phenylephirine + Zink Gluconate
  • Paracetamol + Levocetirizine + Pseudoephedrine
  • Paracetamol + Loratadine + Dextromethophan + Pseudoepheridine + Caffeine
  • Paracetamol + Loratadine + Phenylephrine + Dextromethorphan + Caffeine
  • Paracetamol + mefenamic Acid + ranitidine + Dicyclomine
  • Paracetamol + Pheniramine
  • Paracetamol + Phenylephrine + Chlorpheneramine + Dextromethorphan + caffeine
  • Paracetamol + Phenylephrine + Chlorpheniramine + Zinc Gluconate
  • Paracetamol + Phenylephrine + Desloratadine + Zinc Gluconate + Ambroxol
  • Paracetamol + Phenylephrine + Levocetirizine + Caffeine
  • Paracetamol + Phenylephrine + Triprolidine
  • Paracetamol + Phenylephrine + Triprolidine + Caffeine
  • Paracetamol + Prochloperazine
  • Paracetamol + Prochlorperazine Maleate
  • Paracetamol + Promethazine
  • Paracetamol + Propyphenazone + Caffeine
  • Paracetamol + Pseudoephedrine + Cetrizine
  • Paracetamol + Pseudoephedrine + Dextromethorphan + Cetirizine
  • Paracetamol + Tapentadol
  • Paracetamol+Phenylephrine+Levocetirizine+Sodium Citrate
  • Paracetamol+Pseudoephedrine+Certirizine+Caffeine
  • Permethrin + Cetrimide + Menthol
  • Phenylbutazone + sodium salicylate
  • Phenylephrine + Chlorpheniramine + Paracetamol + Bromhexine + Caffeine
  • Pholcodine + Phenylephrine + Promethazine
  • Pioglitazone 15mg + Metformin 850 mg
  • Pioglitazone 30 mg + Metformin 500 mg
  • Pioglitazone 7.5/7.5mg + Metformin 500/1000mg
  • Pseudoephedrine + Bromhexine
  • Pseudoephedrine + Cetirizine
  • Pseudoephedrine + Dextromethorphan + Cetirizine
  • Rabeprazole + Diclofenac + Paracetamol
  • Rabeprazole + Zinc + Domperidone
  • Rabeprazole + Zinc Carnosine
  • Ranitidine + Domperidone + Simethicone
  • Ranitidine + Magaldrate
  • Ranitidine + Magaldrate + Simethicone
  • Roxithromycin + Serratiopeptidase
  • Salbutamol + Aminophylline + Guaiphensin
  • Salbutamol + Bromhexine + Guaiphenesin + Menthol
  • Salbutamol + Certirizine + Ambroxol
  • Salbutamol + Choline Theophylinate + Ambroxol
  • Salbutamol + Choline Theophylinate + Carbocisteine
  • Salbutamol + Theophylline + Bromhexine
  • Salbutamol+Hydroxyethyltheophylline (Etofylline) + Bromhexine
  • Sildenafil + Estradiol Valerate
  • Tamsulosin + Diclofenac
  • Telmisartan + Metformin
  • Terbutaline + Ambroxol + Guaiphenesin + Zinc + Menthol
  • Terbutaline + Bromhexine + Etofylline
  • Terbutaline + Bromhexine + Guaiphenesin + Dextromethorphan
  • Terbutaline + Etofylline + Ambroxol
  • Terbutaline + N-Acetyl L-Cysteine + Guaifenesin
  • Terpinhydrate + Dextromethorphan + Menthol
  • Thyroid + Thiamine + Riboflavin + Phyridoxine + Calcium Pantothenate + Tocopheryl Acetate + Nicotinamide
  • Thyroxine + Pyridoxine + Folic Acid
  • Tranexamic Acid + Proanthocyanidin
  • Ursodeoxycholic Acid + Silymarin
  • Voglibose + Pioglitazone + Metformin
  • Voglibose+ Metformin + Chromium Picolinate
  • Zinc Carnosine + Magnesium Hydroxide + Dried Aluminium Hydroxide + Simethicone
  • Zinc Carnosine + Oxetacaine
  • Zinc Carnosine + Sucralfate

Human trials begin for a new antimalarial drug: a variant of Chloroquine

The first-in-human study of the new investigational antimalarial drug is being sponsored by the US National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH). This is a phase 1 trial to evaluate the safety and pharmacokinetics of single and multiple ascending doses and effect of food on the pharmacokinetics of the novel antimalarial drug in healthy adults.

The new study, led by principal investigator Michael Cohen-Wolkowiez, M.D., Ph.D., professor of paediatrics at the Duke Clinical Research Institute, is testing an investigational drug called DM1157, invented at Portland State University and developed by DesignMedix, both based in Portland, Oregon.

The novel treatment is a modified form of chloroquine, an established antimalarial drug that kills malaria parasites once they have infected human red blood cells. Many strains of Plasmodium falciparum parasites, which cause the deadliest form of malaria, are now resistant to chloroquine, and the parasites can expel the drug before it can affect them. Like chloroquine, DM1157 interferes with the parasite’s metabolism, but it also inhibits the parasite’s ability to expel the drug. Results of earlier tests in animals suggest that DM1157 could have the same safety and efficacy as chloroquine.

The primary objectives of the study are to:

  1.  assess the safety and tolerability of single doses of DM1157 at levels ranging from 9 mg to 900 mg;
  2. assess the safety and tolerability of DM1157 administered as single daily doses for 3 days at levels ranging from 150 mg to 900 mg;
  3. assess the safety and tolerability of DM1157 administered with or without food

According to the WHO estimates, about 216 million new malaria cases and 445,000 deaths occurred in 2016, primarily among children living in sub-Saharan Africa. Although several approved treatments for the mosquito-borne disease exist, increasing drug resistance among the malaria-causing parasites is diminishing their effectiveness.

DM1157 is designed to provide a cure for drug-resistant malaria and has been shown to overcome drug resistance in blood samples from patients infected with drug-resistant malaria parasites.

Further reading: ClinicalTrials.gov

Aspirin disappoints for avoiding first heart attack and stroke

By Marilynn Marchione for The Associated Press, September 5, 2018

Although it’s been used for more than a century, aspirin’s value in many situations is still unclear

Taking a low-dose aspirin every day has long been known to cut the chances of another heart attack, stroke or other heart problem in people who already have had one, but the risks don’t outweigh the benefits for most other folks, major new research finds.

Although it’s been used for more than a century, aspirin’s value in many situations is still unclear. The latest studies are some of the largest and longest to test this pennies-a-day blood thinner in people who don’t yet have heart disease or a blood vessel-related problem.

One found that aspirin did not help prevent first strokes or heart attacks in people at moderate risk for one because they had several health threats such as smoking, high blood pressure or high cholesterol.

Another tested aspirin in people with diabetes, who are more likely to develop or die from heart problems, and found that the modest benefit it gave was offset by a greater risk of serious bleeding.

Aspirin did not help prevent cancer as had been hoped.

And fish oil supplements, also tested in the study of people with diabetes, failed to help.

“There’s been a lot of uncertainty among doctors around the world about prescribing aspirin” beyond those for whom it’s now recommended, said one study leader, Dr. Jane Armitage of the University of Oxford in England. “If you’re healthy, it’s probably not worth taking it.”

The research was discussed Sunday at the European Society of Cardiology meeting in Munich. The aspirin studies used 100 milligrams a day, more than the 81-milligram pills commonly sold in the United States but still considered low dose. Adult strength is 325 milligrams.

Who’s really at risk?

A Boston-led study gave aspirin or dummy pills to 12,546 people who were thought to have a moderate risk of suffering a heart attack or stroke within a decade because of other health issues.

After five years, 4 per cent of each group had suffered a heart problem—far fewer than expected, suggesting these people were actually at low risk, not moderate. Other medicines they were taking to lower blood pressure and cholesterol may have cut their heart risk so much that aspirin had little chance of helping more, said the study leader, Dr. J. Michael Gaziano of Brigham and Women’s Hospital.

One per cent of aspirin takers had stomach or intestinal bleeding, mostly mild— twice as many as those on dummy pills. Aspirin users also had more nosebleeds, indigestion, reflux or belly pain.

Bayer sponsored the study, and many researchers consult for the aspirin maker. Results were published by the journal Lancet.

Aspirin for diabetes?

People with diabetes have a higher risk of heart problems and strokes from a blood clot, but also a higher risk of bleeding. Guidelines vary on which of them should consider aspirin.

Oxford researchers randomly assigned 15,480 adults with Type 1 or 2 diabetes but otherwise in good health and with no history of heart problems to take either aspirin, 1 gram of fish oil, both substances, or dummy pills every day.

After seven and a half years, there were fewer heart problems among aspirin users but more cases of serious bleeding, so they largely traded one risk for another.

The findings on fish oil

The same study also tested omega-3 fatty acids, the good oils found in salmon, tuna and other fish. Supplement takers fared no better than those given dummy capsules—9 per cent of each group suffered a heart problem.

“We feel very confident that there doesn’t seem to be a role for fish oil supplements for preventing heart disease,” said study leader Dr. Louise Bowman of the University of Oxford.

The British Heart Foundation was the study’s main sponsor. Bayer and Mylan provided aspirin and fish oil, respectively. Results were published by the New England Journal of Medicine.

Other studies are testing different amounts and prescription versions of fish oil, “but I can’t tell people go spend your money on it; we think it’s probably better to eat fish,” said Dr. Holly Andersen, a heart disease prevention specialist at New York-Presbyterian/Weill Cornell who was not involved in the study.

The new research doesn’t alter guidelines on aspirin or fish oil, said Dr. Nieca Goldberg, a cardiologist at NYU Langone Medical Center and an American Heart Association spokeswoman. They recommend fish oil only for certain heart failure patients and say it’s reasonable to consider for people who have already suffered a heart attack.

Source: www.canadianhealthcarenetwork.ca (login required)

Meet the Ester Cousins. Fluticasone furoate (FF) & Fluticasone propionate (FP) – different drugs with different properties

Fluticasone propionate (FP) and fluticasone furoate (FF) are both synthetic glucocorticoid drugs used in the prevention of asthma exacerbations and for the treatment of allergy symptoms and rhinitis.  Based on the assigned glucocorticoid nomenclature, both drugs consist of a common steroidal backbone (fluticasone) and the ester substituent (furoate/propionate). This naming convention wrongly suggests that these derivatives could be ester prodrugs of fluticasone. However, fluticasone 17α esters are remarkably stable and remain attached to the fluticasone backbone even during metabolism. Their pharmacological activity is mediated by the entire molecule (backbone + ester) and they share no common metabolites – neither FF nor FP is metabolised to fluticasone. FF and FP are therefore structurally different compounds with distinct properties.

The furoate and propionate moieties help to significantly increase the glucocorticoid activity of fluticasone and neither of the two is metabolised to Fluticasone (note that fluticasone base does not currently exist as a separate drug moiety). The ester group also contributes to the physicochemical characteristics of the molecule which impact solubility, dissolution rate, tissue affinity, and hence pharmacokinetic and pharmacodynamic properties. The ester derived from 2-furoic acid in FF has been shown to confer higher affinity for both nasal and lung tissue compared with FP and this translates to enhanced lung residency and once-daily efficacy for inhaled FF in asthma. The furoate has a quicker onset of action (8-24 hours) compared to the propionate (3-4 days)

Take away

FF and FP are distinct glucocorticoids and the practice of abbreviating them to fluticasone should be discouraged.

Key differences between FP & FF

  • FP nasal spray FDA approved for ages 4 and up; FF nasal spray approved for ages 2 and up
  • FP inhaled FDA approved for ages 4 and up; FF inhaled approved for ages 5 and up
  • FF has a higher affinity for both nasal and lung tissue compared with FP; this translates to enhanced lung residency and once-daily efficacy in asthma as shown by studies with inhaled FF
  • Once-daily dosing of inhaled FF vs. twice-daily FP

Available FF & FP single-entity preparations

Fluticasone furoate (Nasal spray)

  • For seasonal and perennial allergic rhinitis in patients 2 years of age and older
  • Once-daily dosing
  • Avamys® (GSK)

Fluticasone furoate (Oral inhalation)

  • For maintenance treatment of asthma in patients aged 5 years and older
  • Once-daily dosing
  • Arnuity Ellipta® (GSK)

Fluticasone propionate (Nasal spray)

  • For seasonal and perennial allergic rhinitis in patients 4 years of age and older
  • Once-daily dosing
  • Flixonase® (GSK); Flusort® (Glenmark)

Fluticasone propionate (Oral inhalation)

  • For maintenance treatment of asthma in patients aged 4 years and older
  • Twice-daily dosing
  • Flovent® (GSK)

Fluticasone propionate (Topical)

  • For treatment of corticosteroid-responsive dermatoses
  • Once or twice daily dosing
  • Cutivate® (GSK)

Source: Wiley’s The Clinical Respiratory Journal. Available from: www.ncbi.nlm.nih.gov

Higher is no longer better? Very high levels of ‘Good’ HDL Cholesterol may increase risk of heart attack and death

Very high levels of high-density lipoprotein (HDL or “good”) cholesterol may be associated with an increased risk of heart attack and death, according to research presented today at ESC Congress 2018.

Study author Dr Marc Allard-Ratick, of Emory University School of Medicine, Atlanta, US, said: “It may be time to change the way we view HDL cholesterol. Traditionally, physicians have told their patients that the higher your ‘good’ cholesterol, the better. However, the results from this study and others suggest that this may no longer be the case.”

HDL cholesterol has been considered “good” because the HDL molecule is involved in the transport of cholesterol from the blood and blood vessel walls to the liver and ultimately out of the body, thereby reducing the risk of clogged arteries and atherosclerosis. People with low HDL cholesterol have a greater risk of atherosclerosis and cardiovascular disease. But the protective effect of very high HDL cholesterol has been unclear.

This study, conducted as part of the Emory Cardiovascular Biobank, investigated the relationship between HDL cholesterol levels and the risk of heart attack and death in 5,965 individuals, most of whom had heart disease. The average age of participants was 63 years and 35% were female.

Participants were divided into five groups according to their HDL cholesterol level: less than 30 mg/dl (0.78 mmol/L), 31-40 mg/dl (0.8-1 mmol/L); 41-50 mg/dl (1.1-1.3 mmol/L); 51-60 mg/dl (1.3-1.5 mmol/L); and greater than 60 mg/dl (1.5 mmol/L).

During a median follow-up of four years, 769 (13%) participants had a heart attack or died from a cardiovascular cause. Participants with HDL cholesterol 41-60 mg/dl (1.1-1.5 mmol/L) had the lowest risk of heart attack or cardiovascular death. The risk was increased both in participants with low levels (less than 41 mg/dl) and very high levels (greater than 60 mg/dl) of HDL cholesterol, which produced a U-shaped curve when plotted graphically.

Participants with HDL cholesterol levels greater than 60 mg/dl (1.5 mmol/L) had a nearly 50% increased risk of dying from a cardiovascular cause or having a heart attack compared to those with HDL cholesterol levels 41-60 mg/dl (1.1-1.5 mmol/L).

The associations were consistent even after controlling for other risk factors for heart disease such as diabetes, smoking, and low-density lipoprotein (LDL or “bad”) cholesterol, as well as other factors linked with high HDL cholesterol such as alcohol intake, race, and sex.

The results support findings from several large population-based studies, including a recent publication which found increased cardiovascular and all-cause death when HDL cholesterol reached extremely high levels. Dr Allard-Ratick said: “Our results are important because they contribute to a steadily growing body of evidence that very high HDL cholesterol levels may not be protective, and because unlike much of the other data available at this time, this study was conducted primarily in patients with established heart disease.”

He noted that more research is needed to elucidate the mechanisms of this paradoxical association. “While the answer remains unknown, one possible explanation is that extremely elevated HDL cholesterol may represent ‘dysfunctional HDL’ which may promote rather than protect against cardiovascular disease,” he said.

Dr Allard-Ratick concluded: “One thing is certain: the mantra of HDL cholesterol as the ‘good’ cholesterol may no longer be the case for everyone.”

Source: European Society of Cardiology (ESC). Available at www.escardio.org

A New Drug ARAKODA (Tafenoquine) for Malaria Prophylaxis

The U.S. Food and Drug Administration (FDA) has approved ARAKODA (tafenoquine), an antimalarial, indicated for the prophylaxis of malaria in patients aged 18 years and older. The approved recommended dosage of ARAKODA is completion of the full course of therapy including loading, maintenance, and terminal prophylaxis regimens as follows:

  • Loading regimen: 200 mg once daily with food for 3 days before travel to a malarious area
  • Maintenance regimen: 200 mg once weekly with food 7 days after the last loading dose while in the malarious area
  • Terminal prophylaxis regimen: 200 mg one time only with food 7 days after the last maintenance dose in the week following exit from the malarious area

ARAKODA is contraindicated in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency or unknown G6PD status and when breastfeeding by a lactating woman when the infant is found to be G6PD deficient or if the G6PD status of the infant is unknown, patients with a history of psychotic disorders or current psychotic symptoms (i.e., hallucinations, delusions, and/or grossly disorganized behavior), or patients with known hypersensitivity reactions to tafenoquine, other 8-aminoquinolines, or any component of ARAKODA.

Due to the risk of hemolytic anaemia, test all patients for G6PD deficiency prior to prescribing ARAKODA, and pregnancy testing is recommended for females of reproductive potential prior to initiating treatment. Additional information regarding administration, warnings, and precautions can be found in the full prescribing information linked below.

Mechanism of Action

Tafenoquine, an 8-aminoquinoline antimalarial, is active against all the stages of Plasmodium species that include the hypnozoite (dormant stage) in the liver. Studies in vitro with the erythrocytic forms of Plasmodium falciparum suggest that tafenoquine may exert its effect by inhibiting hematin polymerization and inducing apoptotic-like death of the parasite. In addition to its effect on the parasite, tafenoquine causes red blood cell shrinkage in vitro. The molecular target of tafenoquine is not known.

Antimicrobial activity

Tafenoquine is active against pre-erythrocytic (liver) and erythrocytic (asexual) forms as well as gametocytes of Plasmodium species that include P. falciparum and P. vivax. The activity of tafenoquine against the pre-erythrocytic liver stages of the parasite, prevents the development of the erythrocytic forms of the parasite.

Resistance

A potential for development of resistance of Plasmodium species to tafenoquine was not evaluated. Studies with the erythrocytic forms of P. falciparum strains/isolates suggest a potential for cross-resistance with primaquine, an 8-aminoquinoline. Clinical relevance of such findings is not known

Drug Interactions

In vitro observations suggest the potential for increased concentrations of substrates of OCT2 or MATE transporters which may increase the risk of toxicity of these substrates. Avoid coadministration with drugs that are substrates of OCT2 or MATE transporters (e.g., dofetilide, metformin). If coadministration cannot be avoided, monitor for drug-related toxicities and consider dosage reduction, if needed, based on approved product labeling of the co-administered drug.

Use in Specific Populations

The pharmacokinetics of tafenoquine was not significantly impacted by age, sex, ethnicity, or body weight. The effect of renal or hepatic impairment on tafenoquine pharmacokinetics is unknown. If ARAKODA is administered to patients with renal or hepatic impairment, monitor for adverse reactions associated with ARAKODA.

Efficacy and Safety

Efficacy of ARAKODA was demonstrated in three double-blind, randomized, controlled studies. Additional information regarding efficacy trials can be found in the full prescribing information linked below.

The most common adverse reactions (incidence ≥ 1%) were headache, dizziness, back pain, diarrhoea, nausea, vomiting, increased ALT, motion sickness, insomnia, depression, abnormal dreams, and anxiety.

Full prescribing information available at www.accessdata.fda.gov

A New Tetracycline Antibacterial XERAVA (Eravacycline) for Complicated Intra-Abdominal Infections

The U.S. Food and Drug Administration (FDA) has approved XERAVA (Eravacycline), a fluorocycline antibacterial within the tetracycline class of antibacterial drugs, for the treatment of complicated intra-abdominal infections (cIAI) caused by susceptible microorganisms in patients 18 years of age and older.

XERAVA is not indicated for the treatment of complicated urinary tract infections (cUTI). To reduce the development of drug-resistant bacteria and maintain the effectiveness of XERAVA and other antibacterial drugs, XERAVA should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.

Susceptible microorganisms include: Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter cloacae, Klebsiella oxytoca, Enterococcus faecalis, Enterococcus faecium, Staphylococcus aureus, Streptococcus anginosus group, Clostridium perfringens, Bacteroides species, and Parabacteroides distasonis.

The approved recommended dosage of XERAVA is 1 mg/kg by intravenous infusion over approximately 60 minutes every 12 hours for a total duration of 4 to 14 days. The duration of therapy should be guided by the severity and location of infection and the patient’s clinical response. Additional information regarding dosage and administration can be found in the full prescribing information linked below.

Life-threatening hypersensitivity (anaphylactic) reactions have been reported with XERAVA.

is contraindicated for use in patients with known hypersensitivity to eravacycline, tetracycline-class antibacterial drugs, or to any of the excipients. Discontinue XERAVA if an allergic reaction occurs. The use of XERAVA may cause tooth discoloration and enamel hypoplasia, inhibition of bone growth, andclostridium difficile-associated diarrhea. Additional information regarding these important warnings can be found in the full prescribing information linked below.

Mechanism of Action (MOA) and Pharmacokinetics (PK)

  • MOA: Eravacycline disrupts bacterial protein synthesis by binding to the 30S ribosomal subunit thus preventing the incorporation of amino acid residues into elongating peptide chains.
  • General PK: Eravacycline AUC and Cmax increase proportionally over doses from 1 mg/kg to 3 mg/kg (3 times the approved recommended dosage). Accumulation is approximately 45% following the approved recommended dosage.
  • Distribution: Protein binding of eravacycline increases with increasing plasma concentrations, with 79% to 90% (bound) at plasma concentrations ranging from 100 to 10,000 ng/mL. The volume of distribution at steady-state is approximately 321 L.
  • Elimination: The mean elimination half-life is 20 hours.
  • Metabolism: Eravacycline is metabolized primarily by CYP3A4- and FMO-mediated oxidation.
  • Excretion: Following a single intravenous dose of radiolabeled eravacycline 60 mg, approximately 34% of the dose is excreted in urine and 47% in feces as unchanged eravacycline (20% in urine and 17% in feces) and metabolites.

Drug Interactions

CYP3A Inducers 

Concomitant use of strong CYP3A inducers decreases the exposure of eravacycline, which may reduce the efficacy of XERAVA. Administer XERAVA 1.5 mg/kg every 12 hours for a total duration of 4 to 14days when used concomitantly with a strong CYP3A inducer. No dosage adjustment is warranted in patients with concomitant use of a weak or moderate CYP3A inducer.

Anticoagulant Drugs 

Because tetracyclines have been shown to depress plasma prothrombin activity, patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage.

Use in Specific Populations

No clinically significant differences in the pharmacokinetics of eravacycline were observed based on age (18-86 years), sex, race, or renal impairment.

Patients with Hepatic Impairment 

In patients with severe hepatic impairment (Child-Pugh C), administer XERAVA 1 mg/kg every 12 hours on Day 1, followed by XERAVA 1 mg/kg every 24 hours starting on Day 2 for a total duration of 4 to 14 days. No dosage adjustment is warranted in patients with mild to moderate hepatic impairment (Child-Pugh A and Child-Pugh B).

Efficacy and Safety

Efficacy of XERAVA was demonstrated in two Phase 3, randomized, double-blind, active-controlled, multinational, multicenter trials in adult patients hospitalized with cIAI. Additional information regarding efficacy trials can be found in the full prescribing information linked below.

The most common adverse reactions (incidence ≥ 3%) are infusion site reactions, nausea, and vomiting.

Full prescribing information available at www.accessdata.fda.gov

FDA Approves the First One-Year Contraceptive Fully under a Woman’s Control

The U.S. Food and Drug Administration has approved Annovera® (segesterone acetate and ethinyl estradiol vaginal system), which is a combined hormonal contraceptive for women of reproductive age used to prevent pregnancy and is the first vaginal ring contraceptive that can be used for an entire year.

Description

Annovera combines a new progestin (segesterone acetate) with a widely used estrogen (ethinyl estradiol) into a single reusable ring. It is a soft, reusable flexible silicone ring (2¼ inches diameter) that can be inserted and removed by a woman herself. Left in place for 21 days and removed for 7 days, at which time the woman may experience a period (a withdrawal bleed). This schedule is repeated every four weeks for one year (thirteen 28-day menstrual cycles).

Annovera is indicated to prevent pregnancy for up to a year and does not require refrigeration, which is particularly important for distribution and use in low-resource settings. It is washed and stored in a compact case for the seven days not in use; does not require refrigeration prior to dispensing and can withstand storage temperatures up to 30°C (86°F).

Efficacy & safety considerations

The efficacy and safety of Annovera were studied in three, open label clinical trials with healthy women ranging from 18 to 40 years of age. Based on the results, about two to four women out of 100 women may get pregnant during the first year they use Annovera. Annovera has not been adequately evaluated in women with a body mass index (BMI) greater than 29 kg/m²

All hormonal contraception carries serious risks. Similar to other combined hormonal contraceptives, Annovera has a boxed warning regarding cigarette smoking and serious cardiovascular events. Women over 35 who smoke should not use Annovera. Cigarette smoking increases the risk of serious cardiovascular events from combination hormonal contraceptive use.

Annovera is contraindicated and should not be used in women with:

  • A high risk of arterial or venous thrombotic diseases;
  • Current or history of breast cancer or other estrogen- or progestin-sensitive cancer;
  • Liver tumors, acute hepatitis, or severe (decompensated) cirrhosis;
  • Undiagnosed abnormal uterine bleeding;
  • Hypersensitivity to any of the components of Annovera; and
  • Use of Hepatitis C drug combinations containing ombitasvir/paritaprevir/ritonavir, with or without dasabuvir.

The most common side effects in women using Annovera are similar to those of other combined hormonal contraceptive products and include headache/migraine, nausea/vomiting, yeast infections, abdominal pain, dysmenorrhea (painful menstruation), breast tenderness, irregular bleeding, diarrhea and genital itching.

Full prescribing information available at www.annovera.com/pi.pdf