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Diprophos 7 mg./ 1 ml. 1 ampule

Product Code: Diprophos 7 mg./ 1 ml. 1 ampule
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Product viewed: 109

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What Diprophos is and what it is used for
Diprophos belongs to a group of medicines known as glucocorticosteroids. This group helps to alleviate inflammatory processes. They reduce swelling, redness of the itch, and allergic reactions. They are used as part of the treatment of various diseases.
Diprophas can be used as part of the treatment of various severe conditions that are affected by cortisone medications. These diseases may include diseases of the musculoskeletal system such as various forms of arthritis, bursitis, sciatica, lumbago, bone or deep tissue diseases, allergic conditions such as bronchial asthma, severe hay fever, bronchitis, drug reactions, bites - skin diseases such as inflammation, itching, urticaria (hives), hair loss, psoriasis, scarring, cystic acne or other illnesses judged by your doctor.

2. What you need to know before using Diprophos
Do not use Diprophos:

if you are allergic (hypersensitive) to betamethasone or any of the other ingredients of Dipropos;
if you are allergic (hypersensitive) to other corticosteroid-containing products;
if you suffer from coagulation disorders (clotting);
if you suffer from infectious diseases;
if you suffer from mental conditions;
if you are immunized with a live vaccine;
if you have a fungal infection.
Take special care with Dipropos:

if you are pregnant or breast-feeding;
if you suffer from diabetes or have thyroid problems;
if you have liver disease;
if you have stomach or intestinal complaints;
if you have kidney disease;
if you have seizures, heart problems or blood pressure;
if you have a loss of calcium or muscle weakness;
if you have a pre-existing psychiatric condition;
if you need a vaccination.
Other medicines and Diprophos
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Dose adjustment of these medicines may be necessary while you are being treated with Dipropos.
Similar products include certain barbiturates, antibiotics, hormonal products, diuretics or those for heart or blood disorders. Gastric or intestinal complaints are possible when corticosteroids are taken with medicines that reduce inflammation (anti-inflammatory). Be sure to tell your doctor that you are taking Dipropos if you are undergoing laboratory tests or immunization.

Using Diprophos with food and drink
Corticosteroids with alcohol may cause gastric or intestinal complaints.

Pregnancy and breastfeeding
There is no evidence of safety during pregnancy. Pregnancy should be used in consultation with a doctor.
Dipropose is not recommended for use in breast-feeding women.

Driving and using machines
It has no influence.

Important information about some of the ingredients of Dipropos
Dipropos contains benzyl alcohol, methyl- and propylparaben. Hypersensitivity reactions may occur.
Do not use in children under the age of 3 years.

3. How to use Diprophos
Dipropas is given by injection, usually by your doctor or healthcare professional.
Your doctor will determine the dose according to your individual condition.
Be sure to follow the treatment schedule specified by your doctor.

If you take more Diprofos than you should
Your doctor will make regular assessments of your condition to make sure you are taking the right dose.

If you forget to take Dipropos
Tell your treating physician.
Do not take a double dose to make up for the missed dose.

If you stop using Dipropos
After prolonged treatment, the use of this medicinal product should not be abruptly discontinued; the dose may decrease gradually, at the discretion of your doctor.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS
Like all medicines, Diprophos can cause side effects, although not everyone gets them.
Adverse reactions to Dipropos, which are similar to those reported for other corticosteroids, depend on the dose and duration of treatment.

Side effects that may occur while taking this medicine are the following:
Immune system disorders:

allergic reactions to the medicine and even shock, risk of infection.
Endocrine disorders:

menstrual cycle disorders; development of Cushing's syndrome (as a result of the higher glucocorticoid level); delayed intrauterine development of the fetus, slow growth in children; secondary disorders of the adrenal glands and pituitary glands, especially during stress, such as trauma, surgery or illness; increased blood glucose, exposure to concealed diabetes mellitus, increased insulin requirements, or oral hypoglycaemic drugs in diabetics.
Metabolism and nutrition disorders:

negative nitrogen balance due to increased protein degradation; the accumulation of adipose tissue at certain sites (lipomatosis), which can cause complications, including neurological; weight gain.
Psychiatric disorders:

mood (euphoria), depression, severe depression to psychotic manifestations; personal changes; over-irritability; insomnia.
Nervous system disorders:

convulsions, increased intracranial pressure with optic head edema, usually after treatment; vertigo; headache; tides of heat.
Eye disorders:

Lens haze (rear subcapsule cataracts); increased intraocular pressure, glaucoma, exophthalm.
Gastrointestinal disorders:

Hiccup; peptic ulcer with possible subsequent perforation and haemorrhage; pancreatitis; ballooning the abdomen; oesophageal erosions.
Skin and subcutaneous tissue disorders:

difficult healing of wounds; skin atrophy; thin and easy skin; skin haemorrhage; reddening of the face; increased sweating; suppressed skin tests reactions; reactions such as allergic dermatitis, urticaria, angioneurotic edema.
Musculoskeletal and connective tissue disorders:

muscle weakness, corticosteroid myopathy, loss of muscle mass; aggravation of myasthenic symptoms in myasthenia gravis; osteoporosis; vertebral fractures; aseptic head, shoulder and thigh bone necrosis; pathological fractures of long bones; tendon rupture; joints instability (due to repeated intra-articular application); arthritis due to microcrystalline deposition, occurrence of calcifications.
Water-electrolyte disturbances:

sodium retention, potassium loss, hypokalaemic alkalosis (loss of acidity of body fluids associated with potassium loss); fluid retention; congestive heart failure in risk patients; hypertension.
If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

5. How to store Dipropos
Store below 25 ° C.
Do not freeze.
Store in the original package in order to protect from light.
Keep out of the reach and sight of children.
Do not use Diprophos after the expiry date which is stated on the carton. The expiry date refers to the last day of that month.

6. Package Contents and Additional Information
What Diprohpos contains
The active substance is: 7 mg / ml betamethasone (as 6.43 mg betamethasone dipropionate and 2.63 mg betamethasone sodium phosphate).
The other ingredients are: disodium hydrogen phosphate dihydrate, sodium chloride, disodium edetate, polysorbate 80, benzyl alcohol, methyl parahydroxybenzoate, propyl parahydroxybenzoate, sodium carboxymethylcellulose, polyethylene glycol 3350, hydrochloric acid and water for injections.

What Diprophos looks like and contents of the pack
Diprophos suspension for injection is available in ampoules of 1 ml of 1 and 5 packs in carton.

 

 

 

 

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