Wednesday, April 3, 2019

Ginalgin

Description overdue on 26/11/2014

  • Latin name: Ginalgin
  • ATC code: G01AF20
  • Active substance: Metronidazole, hlorhinaldolu
  • Manufacturer: "ISN Polfa Rzeszow" S.A., Poland
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  • Composition
  • Product form
  • Pharmacological action
  • Pharmacodynamics and pharmacokinetics
  • Indications
  • Contraindications
  • Side effects
  • Candles Ginalgin, instructions for use (method and dosage)
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • During pregnancy (and lactation)
  • Analogs
  • Reviews
  • Price, where to buy

 Ginalgin

Composition

One tablet has active substances metronidazole   of 250 mg hlorhinaldolu   of 100 mg.

Excipients: lactose monohydrate, anhydrous citric acid, sodium starch glycolate (ultramilopektin), rice starch, magnesium stearate, polyethylene glycol 6000.

Product form

Vaginal tablets (2 blisters in a package of 5 pieces in blister).

Pharmacological action

The drug has antibacterial, antibacterial, antifungal, antiprotozoal and trihomonatsidnoe action.

Pharmacodynamics and pharmacokinetics

The preparation includes the active antiprotozoal and antimicrobial substance belonging to 5-nitro-imidazoles , A broad spectrum of action.

Metronidazole   almost completely metabolized in the liver to form inactive derivatives. Poluvyvoda period of 8 hours. Mostly excreted in the urine.

Hlorhinaldolu   in intravaginal application absorbed slightly.

Indications

Candles Ginalgin used in infectious and inflammatory vaginopathy .

Contraindications

The drug should not be taken if:

  • hypersensitivity to metronidazole   and other derivatives nitroimidazole ;
  • hepatic insufficiency ;
  • organic lesions of the central nervous system (including, if epilepsy );
  • are hypersensitive hlorhinaldola ;
  • blood diseases;
  • leukopenia   (including history);
  • incoordination;
  • pregnancy ;
  • breast-feeding .

Side effects

When applying Ginalgin tablets may have the following side effects:

  • rash . itchy skin . hives ;
  • allergic reactions;
  • diarrhea   or constipation . vomiting , Pain in the abdomen spastic character, decreased appetite , Dryness of the mouth, metallic taste in the mouth, taste alteration, nausea ;
  • leukocytosis   or leukopenia . dizziness . headache ;
  • irritation or burning sensation of the penis with a partner;
  • development Candida in the vagina   After discontinuation of the drug;
  • frequent urination ;
  • white, thick vaginal discharge   mucous character with low odor or no;
  • irritation, pain, burning sensation and itching in the vagina.

Occasionally urine may be colored in brown and red.

Candles Ginalgin, instructions for use (method and dosage)

According to the instructions on Ginalgin, the drug is used vaginally - one tablet is administered, preferably in the evening before going to sleep, deep into the vagina for a period of 7 to 10 days. Treatment should start on day 2-4 after menstruation.

Overdose

Data on overdose are not available. If the drug was accidentally received orally, once held gastric lavage   and appointed by means of a enterosorbentnymi properties.

Cooperation

At the same time Ginalginom not recommended to drink alcohol and medicines that contain ethanol . metals . iodine   and antiseptic agents.


Candles can not be used in conjunction with drugs that contain disulfiram   (interval should not be less than two weeks).

Ginalgin increases the risk of rupture Latex contraceptives   (including Condom   and diaphragms ).

Terms of sale

Ginalgin available on medical prescription.

Storage conditions

The drug should be stored at a temperature of from 15 to 25 ° C in a dry place.

Shelf life

Subject to all rules of the drug can be stored up to three years.

Pregnancy

During pregnancy and lactation the drug can not be used.

Analogs Ginalgina

Match code ATC 4th level:
  •  Ginalgin  Lomeksin
  •  Ginalgin  Ornidazole Vero
  •  Ginalgin  Clione-D 100
  •  Ginalgin  Neo-Penotran
  •  Ginalgin  Gyno-Pevaril
  •  Ginalgin  Livarol
  •  Ginalgin  Ginezol
  •  Ginalgin  Antifungol
  •  Ginalgin  Candide
  •  Ginalgin  Ginofort
  •  Ginalgin  Trichopolum
  •  Ginalgin  Flagyl

By analogues of the drug are:

  • Clione ;
  • Metromizol ;
  • Metromikon ;
  • Neo-Penotran ;
  • Pulsiteks .

Reviews Ginalgine

Average rating Ginalgina in various forums - 3.8 out of 5 balls.

According to the reviews of candlelight Ginalgin plus Ginalgina lies in its wide range of action, because, as a rule, when a infection of the vagina , Connected to the main bacteria and other microorganisms. The effectiveness of this drug is not very high, but its use is rarely causes any side effects.

The price of candles Ginalgin

Price Ginalgina in Ukraine is on average from 40 to 100 hryvnia.

In Russia, the average price is 235 rubles Ginalgina.

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Klimaktoplan

Description overdue on 11/28/2014

  • Latin name: Klimaktoplan
  • ATC code: G02CX
  • Active substance: Sepia D2, Sanguinaria D2, Cimicifuga D2, Lachesis D5, Ignatia D3
  • Manufacturer: «DH UNION» for Arzneimittel GmbH & Co. KG. KG, Germany
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  • Composition
  • Product form
  • The pharmacological action of the drug
  • Pharmacodynamics and pharmacokinetics
  • Indications
  • Contraindications
  • Side effects
  • Instructions on Klimaktoplan (Dosage and Administration)
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • Cautions
  • During pregnancy (and lactation)
  • Analogs
  • Reviews
  • Price, where to buy

 Klimaktoplan

Formulation

Cimicifuga . Sepia . Sanguinaria . Lachesis   25 mg each.

Also the Klimaktoplana include inert substances talc, wheat starch, lactose monohydrate, magnesium stearate.

Product form

Valium pills in a gray blister pack of 60, 100 pcs., In a cardboard box

The pharmacological action of the drug

Homeopathic remedy relieves symptoms of complex physical and mental nature, characteristic of pre-, peri- and post-menopausal period. Has an estrogen-like effect, affecting the hypothalamic-pituitary-ovarian That causes a decrease in the secretory function of the anterior lobe pituitary Producing luteinizing hormone .

Decrease of gonadotropins   It ensures the elimination of vegetative-vascular disorders ( nervous irritability . headache . tides . tachycardia . dizziness ) And psycho-emotional states, developing on the background of a simultaneous sharp decline in production estrogen   and increase secretion luteinizing   and follicle stimulating hormone .

Pharmacodynamics and pharmacokinetics

The active ingredients have a complex effect on the body:

  • Cimicifuga   affects hypothalamus , Arresting nervous excitement, depression and feelings of tides.
  • Sepia   normalizes the endocrine function of the pituitary gland, adrenal cortex and ovaries, thereby eases headaches, reduces sweating.
  • Ignatia   normalizes mental condition, relieves general weakness, excessive sweating, pain in the head and flow.
  • Sanguinaria   effective in hot flashes Which are accompanied by palpitations, feeling a rush of blood to the face and headaches by type migraine .
  • Lachesis   has a positive impact on vasomotor disturbances and neurological disorders, relieves the feeling of inner restlessness, insomnia.

Indications

It is used as monotherapy and combined treatment menopausal syndrome   when:

  • tides ;
  • increased sweating ;
  • itching ;
  • nervous tension ;
  • depressive states ;
  • anxiety ;
  • palpitations;
  • dizziness ;
  • insomnia .

For replacement therapy medication Klimaktoplan not intended.

Contraindications

  • hypersensitivity to the drug in the composition;
  • under the age of 18 years.

Side effects of the drug

Allergic reactions, gastrointestinal disturbances (rarely).

Instructions on Klimaktoplan (Dosage and Administration)

The drug is administered orally (hold until resorption) 1-2 tablets for thirty minutes before a meal or after a meal in half an hour, three times per day. The duration of the appointed doctor individually.


Instructions for use Klimaktoplana H   similar.

Overdose

Expressed disturbances of an overdose are not marked.

Cooperation

Interactions with other drugs have been identified. The drug does not preclude the use of other drugs.

Terms of sale

OTC.

Storage conditions

Store at temperatures not above 25 ° C in a dry place inaccessible to children.

Shelf life

4 years.

Cautions

Perhaps a rare temporary deterioration. In such a case, you should stop taking the drug and consult a doctor. In the absence of therapeutic effect within two months of receiving the drug should be abolished and replaced by other drugs prescribed by a doctor.

The effectiveness of the drug, as well as any homeopathic remedy, can have a negative impact receiving stimulants: strong tea, coffee, alcohol.

During pregnancy and lactation

The preparation is not intended for reception at pregnancy   and in lactation .

If during pregnancy Pre-menopausal   the drug should be stopped or taken in the presence of clear indications to estimate the expected benefit to the mother and the risk to the fetus.

Analogs of the drug

Match code ATC 4th level:
  •  Klimaktoplan  Mamoklam
  •  Klimaktoplan  Tazalok
  •  Klimaktoplan  Ovarium Compositum
  •  Klimaktoplan  Gynoflor E
  •  Klimaktoplan  Klimadinon
  •  Klimaktoplan  Klimadinon Uno
  •  Klimaktoplan  Klimalanin
  •  Klimaktoplan  Cyclodynon

On a set of active ingredients unique homeopathic remedy. Structural analogues of the main active ingredient Klimaktoplan not.

Analogs of the pharmacological effect (for the treatment of menopausal and menopausal status): Abyufen . Soyfem . Saguenay . Klimadinon . Klimaksan homeopathic . Klimodien ; Remens . Femoston ; Estrozhel   and several others.

Reviews and Klimaktoplane Klimaktoplane H

Reviews Women

Analyzing the responses of patients to the Internet, we can draw the following conclusions: most of them the positive impact of the drug - reducing the intensity of hot flashes, decrease irritability, improved night's sleep, a decrease in heart rate. However, some women complain of lack of effect, many of them say unstable or short-term effect (first observed improvement, and after a while the symptoms are renewed). Often there are complaints about the disappearance of the tides, but the emergence of tachycardia That causes them to change the drug. Quite a lot of complaints about the weight gain in the range of 3-5 kg.

Doctors about Klimaktoplane and Klimaktoplane H

According to gynecologists drug in the majority of patients it has an effect already in the first month of its receipt. But, in practice, many patients with the instructions of the drug, which reduces the effect.

Price Klimaktoplana where to buy

Price in Moscow pharmacies varies from 350 - 445 rubles / packaging in pharmacies in Ukraine Kiev - 89 - 115 hryvnia / packing. Cost Klimaktoplana H   It is in the same range.

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Esmiya

Description overdue on 11/26/2014

  • Latin name: Esmya
  • ATC code: G03XB02
  • Active substance: Ulipristal (Ulipristal)
  • Manufacturer: Gedeon Richter (Hungary)
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  • Composition
  • Product form
  • Pharmacological action
  • Pharmacodynamics and pharmacokinetics
  • Indications
  • Contraindications
  • Side effects
  • Esmiya, instructions for use
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • Cautions
  • Analogs
  • Babies
  • During pregnancy (and lactation)
  • Reviews
  • Price, where to buy

 Esmiya

Composition

One tablet formulation comprises 5 mg Esmiya ulipristal acetate   - The active ingredient.

As auxiliary substances medicine contains: 43 mg 5 - mannitol; 93, 5 mg - microcrystalline cellulose; 4 mg - Talc; 1, 5 mg - magnesium stearate; 2, 5 mg - sodium croscarmellose.

Product form

The drug Esmiya (Esmya) comes in the form of tablets, one side of which there is engraved «ES5". One package may contain 28 or 84 tablets.

Pharmacological action

Antigestagens.

Pharmacodynamics and pharmacokinetics

The drug Esmiya (Esmya) contains a substance -   ulipristal   synthetic origin, are selective progesterone receptor modulator   and different tissue-specific selective antiprogesteronovym action.

Ulipristal is characterized by a direct effect on endometrium . For most women, the application of 5 mg daily for menstrual cycle , Including sufferers myoma , Does not occur subsequent to this cycle menstrual bleeding . Upon termination of the pills, menstrual cycle Usually recovered within a month.

The direct effect of the drug on endometrium due to some of its specific changes characteristic for this class of drugs and provoked antagonistic action progesterone receptors . In 60% of women taking ulipristal over 3 months, histological changes are weak proliferating inactive epithelium   with related asymmetry of growth and growth stroma , and cystic expansion   glands progestagenic and estrogenic impacts on epithelium . These changes are reversible with the disappearance at the end of treatment, and are not related to endometrial hyperplasia .


In 10-15% of women held therapy with ulipristala It was observed growth of the endometrium Which reached a thickening 16 mm. This thickening also independently disappears at the end of treatment and return to normal menstrual bleeding . If within 3 months after discontinuation of the drug,   thickening of the endometrium   does not come to the state standards, it is necessary to pass an additional examination in order to exclude or confirm other pathologies.

Ulipristal induces apoptosis   and oppresses cell proliferation Thereby providing a direct effect on leiomyoma Leading to their reduction.

The daily intake of 5 mg ulipristala It leads to the guaranteed inhibition of ovulation   the majority of women receiving it, confirming the maintenance of the level of progesterone   at 0, 3 ng / ml. Also, a daily intake of a given dose of the drug is partially reduced the concentration of FSH While leaving the content in the blood plasma Estradiol at the secondary level the follicular phase .

During the 3-month treatment ulipristal It has no effect on the amount of plasma ACTH . prolactin . thyroxine binding globulin .

In preclinical animal studies, while taking multiple doses, there was no threat Toxicity and genotoxicity Products for Human Use. It was noted that the death of fetuses animals when receiving doses greater than 1 mg / kg, and therefore, is not installed Safety ulipristala   towards human embryos . In small doses, which allows you to keep a pregnancy in animals, teratogenic   action was not observed. Also, according to the findings of these studies, there is no direct evidence of the effect of the drug on reproductive ability   animals and their offspring.

Clinical studies of safety and efficacy Esmii at daily doses of 5 and 10 mg, were conducted on volunteers with a female menstrual bleeding   severe, provoked uterine myoma . Compared with the group placebo It was noted clinically significant decrease in the volume of blood loss   Related menstruation , In patients receiving ulipristal , Which allows for faster effective correction of anemia Than when applied alone iron supplementation . Patients receiving group ulipristala , Lowering the amount of blood loss was comparable with the group of patients treated with Leuprorelin (GnRH agonist). In most cases resulted in a reception Esmii cessation of bleeding   during the first week of treatment (developing amenorrhea ). MRI studies in this group showed a significant a decrease uterine fibroids As compared with the group placebo . Carrying US control   at the end of treatment (Week 13), in order to establish reduce the size of uterine fibroids It showed preservation of its parameters in a group ulipristala for 25 weeks, compared with some increase in its dimensions in the group Leuprolide .

Upon receiving ulipristala in a single dose of 5 mg, a rapid absorption of the drug from reaching Cmax after 60 minutes at - 23 ± 5 14, 2 ng / ml plasma concentrations of 61, 3 31 ± 7 ng / ml. Ulipristal undergoes rapid transformation with the release pharmacologically active metabolite While after 60 minutes reached Cmax 4 9 ± 4 ng / ml and a plasma concentration of 26 ± 12 ng / ml.

When receiving 30 mg Esmii during breakfast high in fat, 45% reduction was observed Cmax, up to 3 hours and an increase in Tmax 25% increase in plasma concentrations, both the ulipristala And its metabolite Unlike fasting. With daily pill, this effect is not regarded as significant.

The plasma protein ulipristal It binds to 98% or even more.

Metabolism takes place with the participation of cytochrome P450 with the final selection di-N-demethylated metabolite .

In more output intestines less (about 10%) by the kidneys. T1 / 2 at a dose of 5 mg, about 38 hours, with an average clearance of about 100 l / h.

Indications

Pre-treatment   manifestations uterine fibroids   moderate to severe in women of reproductive age who have attained 18 years of age, duration of not more than 3 months.

Contraindications

Conducting drug therapy is contraindicated Esmiya:

  • at hypersensitivity ulipristalu to the patient or other components of the tablet;
  • at Vaginal bleeding   undiagnosed nature or for reasons unrelated to the uterine cancer ;
  • at malignancies   cervix, ovaries, uterus, mammary glands;
  • at severe bronchial asthma That is not treatable oral corticosteroids ;
  • when not reaching the age of 18 years;
  • during periods breast-feeding   and pregnancy ;
  • in the case of alleged course of therapy than 3 months (because of the lack of reliable data on the impact of ulipristala on the body, for over this period).

Carefully:

  • renal disease and / or liver disease;
  • bronchial asthma .

Side effects

CNS:

  • emotional disturbances;
  • headache ;
  • anxiety;
  • dizziness .

Bodies of the digestive tract:

  • nausea ;
  • abdominal pain;
  • dyspepsia ;
  • flatulence ;
  • dryness of the mouth;
  • constipation .

The organs of hearing:

  • vertigo .

Respiratory system:

  • nosebleeds .

Skin and subcutaneous tissue disorders:

  • increase sweating ;
  • appearance acne ;
  • lesions of the skin.

Musculoskeletal system:

  • soreness   muscles and bones;
  • pain in the back.

Genito-urinary system and mammary glands:

  • amenorrhea ;
  • urinary incontinence;
  • thickening of the endometrium ;
  • metrorrhagia ;
  • tides ;
  • education ovarian cysts ;
  • pelvic pain;
  • soreness . increase , Tension Breast ;
  • vaginal discharge ;
  • cyst rupture   ovary.

Others:

  • weight gain;
  • fatigue;
  • swelling ;
  • asthenia .

Laboratory evidence:

  • increase of blood cholesterol and triglycerides .

In clinical trials, the most frequent adverse events, of which 10-15% occupied thickening of the endometrium In most cases their own passing after discontinuation of treatment; 12-13% - tides ; 6, 4% - headache   mild or moderate in severity; 15% - ovarian cysts , Disappear spontaneously over several weeks; uterine bleeding Which in some cases require surgery.

Esmiya, instructions for use

Instructions on Esmiyu recommends daily intake of one-time first tablet orally (inside), regardless of the meal.

Time of the first week of therapy is limited menstrual cycle . This period should start taking pills Esmiya, preferably at the same time of day.

At the time pass reception the next tablet should be taken as soon as possible, within 12 hours. If you exceed this time limit, passed the acceptance and continue the course of treatment followed by tablets at one time.

Due to the lack of experience with Esmii over time exceeding 3 months, this term is only valid for the treatment.

Overdose

Full information on the possibility of overdose Esmiya and the consequent negative manifestations, for the time being does not exist. Thoroughly aware that receiving a single 200 mg dose and 50 mg daily doses for 10 days did not result in serious or grave condition of the patient.

Cooperation

Hormonal birth control pills As well as affect Esmiya progesterone receptors   and may reduce the effects of each other, and therefore, not recommended for combined use.

Combines the reception and Esmii inhibitors of CYP3A4   moderate ( Erythromycin ) And powerful ( Nefazodone . Ritonavir . Ketoconazole ) Steps could trigger a significant increase in plasma concentration ulipristala . For this reason it is recommended to use them together. Receiving inhibitors of CYP3A4   benign not significantly affect the pharmacokinetics Esmii, and therefore does not require adjusting the dose of the latter.

Receiving inducers of CYP3A4 It leads to a decrease of the plasma content ulipristala . Therefore, concomitant use inducers of CYP3A4   powerful action ( Rifampicin . Phenytoin . Carbamazepine , Means including St. John's wort ) not recommended.

During absorption in the walls of the digestive tract ulipristal able inhibit P-gp Thereby increasing plasma concentrations of substrates of P-gp . In this regard, it is not recommended, and coadministration Esmii substrates of P-gp   ( Digoxin . Dabigatran ).

In the future clinical use Esmii may identify other drug interactions.

The patient preparing to undergo therapy with Esmii is obliged to inform your doctor about all the measures it funds as of prescription and OTC list.

Terms of sale

Pharmacies Russia to purchase the drug Esmiya required to present a doctor's prescription.

Storage conditions

Tablets Esmiya drug should be stored in the original packaging at an ambient temperature of 30 ° C.

Shelf life

When stored product shelf life is 2 years.

Cautions

The drug Esmiya may be appointed only after a thorough examination in order to confirm indications and contraindications exceptions pregnancy .

During therapy is recommended to use additional barrier methods of contraception As efficiency hormonal contraceptives   It can be reduced, as the action of the drug.

Although reliable data on the impact of renal failure   on elimination ulipristala No, I do not recommend its acceptance by patients with the disease, especially in severe form, without the supervision of a physician. These recommendations apply to patients with hepatic insufficiency   moderate to severe, as it is assumed the impact of this disease on elimination ulipristala .

Duration of therapy should not exceed 3 months.

Patients taking Esmiyu should be made aware that the effect of the drug is usually accompanied by significant reduction in menstrual blood loss   or leads to amenorrhea during 10 days of therapy. At the expiration of this period, in the case of continuing profuse bleeding , You need to see a doctor. In general, normal menstrual cycle   He returned one month after discontinuation of treatment.

The majority of patients treated with the drug Esmiya, observed anovulation . Nonetheless, fertility in therapy ulipristalom It has not been studied.

Analogs Esmii

Match code ATC 4th level:
  •  Esmiya  Zhenale
  •  Esmiya  Mifegin
  •  Esmiya  Miropriston
  •  Esmiya  Ginepriston
  •  Esmiya  Mifepristone
  •  Esmiya  Penkrofton

Analogs ulipristala belonging to one group of pharmacological and similar but not identical in the main action, represented by the following drugs:

  • Agesta ;
  • Ginepriston ;
  • Zhenale ;
  • Gynestril administration ;
  • Miropriston ;
  • Mifepreks ;
  • Mifegin ;
  • Mifepristone ;
  • Penkrofton ;
  • Mifolian .

Babies

Due to the lack of research, therapy with Esmii in patients under 18 years old are not carried out.

During pregnancy and lactation

At this time, the periods breast-feeding   and pregnancy are contraindications to therapy ulipristalom .

Reviews Esmii

Currently, treatment uterine fibroids   Esmiya with the drug has not yet reached the scale, after which it is possible to make an unambiguous conclusion about the advisability of the appointment of its mass. Reviews of doctors about the drug often cautious, although some experts say about Esmii, as a real "breakthrough" in the treatment of this disease, most doctors are positioning it as a cure for preoperative   patient in order to reducing the size of fibroids   and correction of anemia   by reducing or stopping uterine bleeding .
It is proved that, in many cases, the possibility to prepare a tablet Esmii uterus for surgery so that subsequently save reproductive function . Among the side effects, doctors usually say tides Especially at the beginning of treatment, discomfort . headache   and cyst formation That confirm the ratings of patients taking the drug.

Reviews Esmii in forums to negotiate ways and methods treatment of uterine Also mixed. Mostly women discuss failure, in their view, the effectiveness of Esmii and associated with its intake side of manifestation. Also not unimportant role in the discussion covers the cost of the drug, which today is quite high. The majority of patients treated with ulipristal They remained dissatisfied with its action and lots of side effects. In fairness it should be noted that few of them had a full course of treatment takes 3 months, and often stopped therapy at some point or another.

In summary, an unequivocal positive or negative conclusion about the drug Esmiya can be done. On the successful struggle against uterine fibroids   influenced by many factors, ranging from the time of its discovery, and the size and finishing skills and intuition of the attending physician. In any case, we hope that further experience with ulipristala It will allow him to take the appropriate niche treatment of uterine fibroids   and really show the positive results of therapy.

Price Esmii where to buy

Price Esmii pharmacies in Russia ranges from 7000 - 9000 rubles.

This drug you can buy in Moscow, about 7,500 rubles.

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Sunday, March 31, 2019

Bivalos

Description overdue on 09/26/2014

  • Latin name: Bivalos
  • ATC code: M05BX03
  • Active substance: Strontium ranelate (Strontium ranelate)
  • Manufacturer: Les Laboratoires Servier (France)
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  • Composition
  • Product form
  • Pharmacological action
  • Pharmacodynamics and pharmacokinetics
  • Indications
  • Contraindications
  • Side effects
  • Instructions for use Bivalos (method and dosage)
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • Cautions
  • Analogs
  • Babies
  • During pregnancy (and lactation)
  • Reviews
  • Price, where to buy

 Bivalos

Composition

One sachet contains 2532 milligrams of the drug Strontium ranelate hydrate   or 2000 milligrams of active substance is equivalent to anhydrous strontium ranelate . As part of the drug Bivalos contain adjuvants such as: mannitol, aspartame, and maltodextrin.

Product form

Bivalos produced in the form of pale yellow powder. The drug is used for the preparation of opaque white suspension. In one carton tend to be 7, 14, 28, 56, 84 or 100 sachets, each containing 2 grams of the active drug compound.

Pharmacological action

The drug helps to correct the metabolism of cartilage and bone.

Pharmacodynamics and pharmacokinetics

The results of the research in the face invitro (i.e., in vitro), it was found that strontium ranelate   promotes formation   bone . Besides being useful compound involved in   collagen synthesis and stimulates the production of precursors osteoblasts .

Bivalos reduces speed bone resorption Thus kupiruya the process of osteoclast differentiation . Under the influence of the drug compound the process of destruction of bone changes in the direction of its formation. One can say that the drug triggers recovery of bone tissue in the human body during osteoporosis.
In long-term therapeutic treatment (over three years), patients have an increase in the level of biochemical markers Responsible for bone formation (I C-terminal propeptide procollagen)   as well as reduced maintenance Markers Which leads to bone resorption (N-terminal and C-terminal telopeptide).


Bivalos effective in treating   postmenopausal osteoporosis in women during which increases the risk fractures . The drug has also shown excellent results when used during osteoarthritis . The active agent is involved in the development of cartilage matrix As well as the impacts on human chondrocytes Thus slowing down the process of tissue destruction. Thanks inhibition of subchondral bone resorption tissue   the drug has a positive effect on the pathophysiology of osteoarthritis .

Indications

The drug used in the treatment of:

  • Osteoporosis in the menstrual period in women for the prevention and prevention   fractures;
  • Osteoporosis hip or knee joints;
  • osteoporosis in men.

Besides Bivalos used as part of a   therapeutic treatment of fractures , eg, hip .

Contraindications

The drug is contraindicated in:

  • hypersensitivity;
  • VTE (venous thromboembolism);
  • vein thrombosis;
  • pulmonary embolism;
  • immobilization;
  • coronary artery disease;
  • artery and cerebrovascular diseases;
  • hypertension.

Besides Bivalos forbidden to use in the treatment of patients who have not yet reached 18 years of age. With extreme caution and only under medical supervision, you can use the drug to patients suffering from renal failure And when venous thromboembolism .

Side effects

During use of the drug may occur following side effects gastrointestinal tract, nervous and cardiovascular system:

  • headache;
  • convulsions;
  • impaired memory and consciousness;
  • diarrhea;
  • vomiting;
  • nausea;
  • diarrhea;
  • stomatitis;
  • mucous (eg mouth sores);
  • venous thromboembolism.

On top of that there may be different allergic reactions   when using this drug, and expressed in appearance rashes on the skin, itching, hives, dermatitis or eczema.

Instructions for use Bivalos (method and dosage)

In accordance with the instructions on Bivalos formulation intended for oral administration. Before direct use should be prepared from the powder in a sachet liquid drug suspension Which it is recommended to use at bedtime. And immediately after taking the medicine should take a horizontal position for maximum therapeutic effect.

The recommended daily dosage is 2 grams Bivalos (ie one sachet). To avoid overdose should not arbitrarily increase the dose of medication without consulting your doctor, since the course of treatment is designed for a long period of time. To prepare the suspension to dissolve one sachet Bivalos at least 1/3 cup of water.

Due to the fact that many of the foods and food supplements containing in its composition   calcium   their use should be avoided for at least two hours before taking the drug, because it reduces absorption of strontium ranelate And, consequently, its effectiveness. During the administration of the drug in patients with shortages vitamin D , and   Calcium   should be given additional medicines that will saturate the body with the necessary elements of the patient.

Overdose

Even though in excess of recommended dosages of the drug in patients rarely have side effects in overdose should still take measures to reduce absorption in the stomach of the active drug contained in the chemical composition of the drug. To do this, use milk or dairy products. In addition, it is recommended to vomit from the body to remove residues of the active compounds.

Cooperation

To avoid reducing the efficiency of BIVALOS should not be taken for at least two hours after eating milk or milk products. The same rules should be followed while using strontium ranelate and antacid drugs. It is worth noting that the efficacy antibiotics,   belonging to quinoline and tetracycline drugs Significantly reduced when concomitantly with Bivalos.

Terms of sale

Buy Bivalos a pharmacy only if you have a prescription.

Storage conditions

Although special storage conditions for the drug is not provided, it is best to store Bivalos dry and inaccessible place for children.

Shelf life

3 years.

Cautions

When using this drug in the treatment of patients with renal failure   should constantly monitor the proper functioning kidney . Since taking Bivalos can develop VTE (venous thromboembolism)   and the reasons for this phenomenon have not been installed by specialists until now, physicians should be aware of this factor in the appointment of the drug to patients at risk.

When receiving the drug may exhibit different skin reactions , eg Stevens-Johnson syndrome, drug rash, eosinophilia, epidermal necrolysis , and DRESS-syndrome . If you have symptoms of the above ailments should immediately stop using Bivalos.

As contained in the product   strontium   affects the results colorimetric Research   attendance   Potassium blood or urine, for the most accurate estimate, use other methods, such as spectrometry, atomic emission or   absorption atomic spectrometry and others.

Contained in the chemical composition Bivalos Aspartame   can provoke unwanted adverse reactions in patients phenylketonuria . The drug does not affect the ability of people to accept it, to drive vehicles or does not interfere with work with dangerous to life and health mechanisms or units.

Analogs Bivalos

Match code ATC 4th level:
  •  Bivalos  Osteogenon

The list includes the following unique Bivalos drugs:

  • Strontium ranelate ;
  • Stromos ;
  • Strait ;
  • Osteogenon ;
  • Iksdzheva .

Patients leave the various reviews Bivalos analogues, however, as on the preparation itself.

Babies

The drug is not recommended for use in the treatment of pediatric patients.

During pregnancy (and lactation)

This drug is not recommended for use in the treatment of pregnant   women. It is strictly forbidden to take during Bivalos Lactation As contained in a preparation   strontium ranelate   excreted in breast milk.

Reviews Bivalos

Although the bulk of the patients on Bivalos reviews are positive, some patients taking the drug, a negative to say about this drug. Negative feedback on the forums Bivalos still occur, albeit less frequently, and are reduced primarily to the fact that people complain about the list of contraindications and side effects of the drug.

Price Bivalos where to buy

The cost of the drug depends on the region, but you can buy it in the vast majority of pharmacies. Average price Bivalos in Ukraine (pack with 28 sachets) up to 400 UAH.

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Treatment with artrofoon

Description overdue on 10/26/2014

  • Latin name: Arthrofon
  • ATC code: L03
  • Active substance: Affinity-purified antibodies to human tumor necrosis factor alpha (FNOalfa)
  • Manufacturer: NPF Materia Medica Holding Company (Russia)
Photos of the drug
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  • Composition
  • Product form
  • Pharmacological action
  • Pharmacodynamics and pharmacokinetics
  • Indications treatment with artrofoon
  • Contraindications
  • Side effects
  • Instructions for use treatment with artrofoon (method and dosage)
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • Cautions
  • Analogs
  • Babies
  • During pregnancy (and lactation)
  • Reviews
  • Price, where to buy

 Treatment with artrofoon

Composition

The structure 1 includes 3 mg tablets antibodies FNOalfa (human), - the active substance.

Additional ingredients:

  • 267 mg - lactose;
  • 30 mg - microcrystalline cellulose;
  • 3 mg - magnesium stearate.

Product form

Valium tablets with a facet and Valium, white or cream-colored. On opposite sides of the inscription «ARTHROFON» and «MATERIA MEDICA».

In the audio pack 20, 40, 50, 75 or 100 tablets.

Pharmacological action

Anti-inflammatory, analgesic.

Pharmacodynamics and pharmacokinetics

Tablets are a treatment with artrofoon   Homeopathic medicines Exhibiting anti-inflammatory and analgesic effect and is used for the treatment of inflammatory processes   musculoskeletal system.   The treatment leads to an increase in supply of fabrics, to enhance the microcirculation and replication inhibition of inflammatory mediators. Turning to treatment with artrofoon regimens inflammatory degenerative pathologies of joints, leads to a reduction in the time course of an acute disease, but also to reduce the dosage of other drugs used in the treatment (often NSAIDs ).

Indications treatment with artrofoon

Indications allow the use of a formulation as in monotherapy (during remission primary disease), and in combination with other drugs (during exacerbation underlying disease).


More often prescribed for the treatment of treatment with artrofoon rheumatoid arthritis, osteoarthritis (including spondylarthrosis)   and other painful conditions of the joints.

Contraindications

In the absence of reliable data on the effects of treatment with artrofoon patients under 18 years of age, it is not used in this age category.

Also, a contraindication to its purpose is hypersensitivity   tablet ingredients to a patient.

Side effects

Might appear hypersensitivity reactions   the constituents of the drug.

Instructions for use treatment with artrofoon (method and dosage)

The tablets are taken orally treatment with artrofoon ( sublingually ). It recommends a single dose of two tablets under the tongue until they are completely dissolved. In order to achieve maximum efficiency you should not crush or chew the tablets. The preferred time taking the drug - morning and evening (2 times a day). Generally, therapy lasts no more than six months.

In severe pain, manual treatment with artrofoon in the first 2-4 weeks, allows 4-time receiving 2 tablets per day, with the holding of parallel treatment. When relieving pain gradually moving to the recommended dosage.

Overdose

You may experience dyspepsia Caused by members of the drug ingredients.

Cooperation

Hitherto incompatibilities with other drugs was observed.

It is possible to combine a reception   NSAIDs.

In parallel, it can be used analgesic and antiinflammatory ointment, gel or cream.

Terms of sale

Over the counter.

Storage conditions

The temperature is not above 25 ° C.

Shelf life

36 months.

Cautions

After initiation of therapy, 3-5 hours may a moderate increase in inflammation and pain That is, most often, not in need of correction regimens. In some cases, you can temporarily reduce the dose by half.

Treatment with artrofoon include lactose, and therefore, it is undesirable to prescribe to patients suffering lactase deficiency, galactose malabsorption syndrome or   glucose galactosemia.

Analogs

Match code ATC 4th level:
  •  Treatment with artrofoon  Polioksidony
  •  Treatment with artrofoon  Derinat
  •  Treatment with artrofoon  Interferon
  •  Treatment with artrofoon  Neovir
  •  Treatment with artrofoon  Nazoferon
  •  Treatment with artrofoon  Timalin
  •  Treatment with artrofoon  Viferon
  •  Treatment with artrofoon  Timogen
  •  Treatment with artrofoon  Roncoleukin
  •  Treatment with artrofoon  TSikloferon
  •  Treatment with artrofoon  Broncho-Vaks
  •  Treatment with artrofoon  Infagel
  •  Treatment with artrofoon  Uro-Vaks
  •  Treatment with artrofoon  IFN-EU-Lipint
  •  Treatment with artrofoon  IFN-EU
  •  Treatment with artrofoon  IFN-Lipint
  •  Treatment with artrofoon  Altevir
  •  Treatment with artrofoon  Algeron
  •  Treatment with artrofoon  Laferobion
  • Alflutop;
  • Bischofite;
  • Discus compositum;
  • Polikatan;
  • Sinovial;
  • Teraflex;
  • Traumeel S;
  • Hondrofleks;
  • The purpose of the T etc.

Babies

I do not recommend the appointment of treatment with artrofoon 18 years.

During pregnancy (and lactation)

Not studied the safety of therapy when treatment with artrofoon pregnancy and   Lactation . If necessary, its use should be weighed against the risk / benefit.

Reviews of treatment with artrofoon

There is no clear answer about the effectiveness and appropriateness of the destination of the drug treatment with artrofoon. Reviews of doctors who use it in their practice, divided approximately equally.

Some people watch more rapid improvement of the patient during treatment with artrofoon appointment in treatment, the effectiveness of other therapies require other drugs, and does not notice the changes of the disease, both in its application and without. Possibly, depending on the individual characteristics of each patient, as well as the placebo effect.

Treatment with artrofoon price, where to buy

The price depends on the amount of drug included in the packaging of tablets, as well as the region and the pharmacy network.

If you decide to purchase a pill treatment with artrofoon, the price of 100 pieces, on average - 250 rubles.

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Three-regolith

Description overdue on 09/15/2014

  • Latin name: Tri-Regol
  • ATC code: G03AB03
  • Active substance: Ethinyl estradiol (Ethinylestradiol), Levonorgestrel (Levonorgestrel)
  • Manufacturer: Gedeon Richter (Hungary)
Photos of the drug
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  • Composition
  • Product form
  • Pharmacological action
  • Pharmacodynamics and pharmacokinetics
  • Indications
  • Contraindications
  • Side effects
  • Instructions for use Three Regola (method and dosage)
  • Overdose
  • Cooperation
  • Terms of sale
  • Storage conditions
  • Shelf life
  • Reviews
  • Price, where to buy

 Three-regolith

Composition

Tablets include surfactants such as ethinylestradiol   and levonorgestrel .

Additional components include: talc, colloidal silicon dioxide, lactose monohydrate, corn starch, magnesium stearate.

The shell consists of sucrose, talc, titanium dioxide, macrogol 6000, red iron oxide, calcium carbonate, copovidone, colloidal silicon dioxide, povidone, carmellose sodium.

Product form

Three Regoli produced in the form of coated tablets.

Pharmacological action

Three-phase oral contraceptive.

Pharmacodynamics and pharmacokinetics

The drug belongs to a combined contraceptive drugs.

Levonorgestrel   reduces production gonadotropins , Resulting in slower and ovum matures ovulation   It does not occur.

Ethinylestradiol In turn, increases the viscosity of cervical mucus and reduces the passage of sperm into the uterus.

In addition, the three-regolith helps to normalize the menstrual cycle, as complementary level endogenous hormones .

The drug is well absorbed in the intestine upon oral administration. Processed in the intestine and liver and then eliminated via the kidneys and intestines.

Indications

The need for oral contraception. Treatment of disorders of the menstrual cycle.

Contraindications

Use of the drug is contraindicated in:

  • over the age of 40 years;
  • pregnancy   and breast-feeding ;
  • Heavyweight itching   and idiopathic jaundice   pregnant women in history;
  • gallbladder disease;
  • smoking at the age of 35 years;
  • thromboembolism   and thrombosis And predisposition thereto;
  • diabetes   severe;
  • improper fat metabolism;
  • molar pregnancy ;
  • migraine ;
  • otosclerosis   with hearing problems;
  • recent surgery;
  • deficiency of the enzyme, which is needed to digest lactose milk;
  • Hypersensitivity to the drug;
  • liver disease;
  • severe cardiovascular and cerebrovascular changes in history;
  • Vaginal bleeding   undetermined etiology;
  • sickle cell   and hemolytic anemia ;
  • malignancies;
  • chronic colitis ;
  • Marfan syndrome ;
  • phlebitis ;
  • extensive injuries.

With care, this drug should be used when:

  • asthma ;
  • Chronic venous insufficiency   the lower extremities;
  • epilepsy ;
  • small chorea ;
  • porphyria ;
  • uterine cancer ;
  • depression ;
  • diabetes in step compensation (in the absence of vascular complications);
  • multiple sclerosis ;
  • hypertension   (BP up to 160/100 mm Hg. V.);
  • tetany ;
  • mastitis ;
  • tuberculosis ;
  • lack of regular menstrual cycle during adolescence.

Side effects

Adverse effects Three Regola usually following: discomfort when using contact lenses, intermenstrual bleeding, weight changes, nausea, fluid retention, changes in libido, breast sense of tension, acne . irritability . depression , Irritability, breast pain, headache . migraine , Blurred vision, gipomenoreya . amenorrhea .


These side effects are temporary and without special treatment. In rare cases can develop tumors appear lupus erythematosus . ulcerative colitis . hepatitis . Crohn's disease . jaundice .

Furthermore, increasing the number of infrequently observed triglycerides   plasma glucose tolerance reduction, fatigue, increased blood sugar, chorea . otosclerosis . embolism   pulmonary artery thrombophlebitis   deep veins, increased blood pressure, venous thromboembolism . thrombosis , Vomiting, cholelithiasis . diarrhea . pancreatitis , Skin rashes, exudative erythema multiforme , hair loss, hives . erythema nodosum , Change vaginal secretion, chloasma The appearance of secretion from the mammary glands, fungal infections vagina.

There may be side reactions such as dizziness , Worsening epilepsy . hypertrichosis . seborrhea , A feeling of heaviness in the legs.

Instructions for use Three Regola (method and dosage)

Instructions for Three-Regoli discloses that tablets should be taken in one day at the same time. The course from the first day of menstruation and is designed for 21 days. After this has to be a break week for menstrualnopodobnoe bleeding. Then start taking the tablets again on the first package (even if the bleeding is still present). First you need to take 6 pink tablets and then - and after 5 white - 10 yellow.

The order of taking the medicine packaging specified numbers and arrows. If one pack contains 28 tablets after ingestion DY should proceed to brown (do not contain hormones), and the next course should start 28 days without interruption.

If a pill is missed (passed more than 36 hours), reliable contraceptive protection is not guaranteed. On the first and second week of the cycle in the case of the missing instructions for use Three Regola Council adopted the next day just 2 tablets.

If you missed just two pills in a row, following 2 days you need to take 2 tablets, then continue the course, as usual. When you pass on the third week of the course seven-day break is not done.

Skipping tablets does not relate to brown. They contain iron, and they are used to maintain continuity.

If the drug is prescribed for and its dosage is adjusted individually.

Overdose

At doses in excess of the patients have nausea . headache . uterine bleeding . In this case, you must consult your doctor immediately. Treatment is symptomatic, gastric lavage.

Cooperation

Caution is advised to take three-regolith in conjunction with:

  • Ampicillin . Chloramphenicol .   Penicillin . tetracyclines . Dihydroergotamine . Phenylbutazone . Rifampicin . Neomycin . sulfonamides Some anticonvulsants and tranquilizers, Ketoconazole   - May decrease the effectiveness of contraception;
  • tricyclic antidepressants . beta-blockers . Maprotiline   - Possibly increasing bioavailability and toxicity of these agents;
  • Bromocriptine   - Can reduce the effectiveness;
  • anticoagulants Derived indandiona   or coumarin   - May be necessary to monitor the prothrombin time, adjusting dosages;
  • antidiabetic medicines for oral use, Insulin   - You may need dosage adjustments;
  • hepatotoxic   It means - increased risk of increased hepatotoxicity.

Terms of sale

The drug is sold by prescription only.

Storage conditions

Means must be kept out of the reach of small children. The temperature must be below 25 0C.

Shelf life

Shelf life - 5 years.

Reviews of Tri-regolith

Birth control pills Tri-regolith get a variety of responses, as well as most other hormonal contraceptives. For some, they fit perfectly, and someone gets a lot of unwanted side effects. While most reviews of Tri-regolith is still positive. Some girls even "prescribe" it to themselves, without consulting with experts. And in most cases, problems with pregnancy after the cancellation rate was observed.

According to doctors about three-regolith is usually positive. They are often prescribed to patients for the normalization of the menstrual cycle. Doctors about three-regolith boil down to the fact that it is relatively harmless remedy for little money. However, the effect of oral contraceptive use is very individual. Some experts have neglected the need to analyze, so it also happens that the drug is not suitable for a number of indicators of patients who appointed him. This leads to undesirable side reactions. So appoint a three-regolith should be only after the relevant tests.

Price three-Regola where to buy

Price three-Regola compared with a number of similar funds is considered very affordable. That is why it is often recommended specialists. Price three-Regola in packaging designed for the tablet 21, an average of about 200 rubles.

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