Thursday, April 12, 2012

Vaginal anti-infectives


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Vaginal anti-infectives are available as creams, pessaries (tablets), gels or solutions to treat either bacterial or fungal vaginal infections. Vaginal antifungal products are used to treat vaginal thrush. Antibacterial vaginal products are used for bacterial infections such as bacterial vaginosis. Other products are used to manage irritation or minor soreness.

See also

Medical conditions associated with vaginal anti-infectives:

  • Acne
  • Bacterial Vaginitis
  • Cutaneous Candidiasis
  • Fungal Infection Prophylaxis
  • Oral Thrush
  • Perioral Dermatitis
  • Rosacea
  • Tinea Corporis
  • Tinea Cruris
  • Tinea Pedis
  • Tinea Versicolor
  • Vaginal Yeast Infection

Drug List:

Saturday, April 7, 2012

Miscellaneous topical agents


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Topical agents are used locally, where the medicine is applied on the area being treated. For example creams, ointment and lotions are applied topically on the skin. Eye drops are instilled directly into the eyes.


The miscellaneous topical agents listed here are mostly agents used topically to treat skin conditions.

See also

Medical conditions associated with miscellaneous topical agents:

  • Acne
  • Actinic Keratosis
  • Allergic Urticaria
  • Alopecia
  • Anal Itching
  • Atopic Dermatitis
  • Back Pain
  • Basal Cell Carcinoma
  • Burning Mouth Syndrome
  • Burns, External
  • Bursitis
  • Cold Symptoms
  • Cutaneous T-cell Lymphoma
  • Dandruff
  • Dermatitis
  • Dermatologic Lesion
  • Dermatological Disorders
  • Diabetic Nerve Damage
  • Diaper Rash
  • Dry Skin
  • Eczema
  • Epicondylitis, Tennis Elbow
  • Eyelash Hypotrichosis
  • Herpes Simplex
  • Hirsutism
  • Hyperhidrosis
  • Inflammatory Conditions
  • Kaposi's Sarcoma
  • Melasma
  • Mucositis
  • Muscle Pain
  • Nasal Congestion
  • Osteoarthritis
  • Pain
  • Period Pain
  • Perioral Dermatitis
  • Peripheral Neuropathy
  • Persisting Pain, Shingles
  • Photoaging of the Skin
  • Pityriasis rubra pilaris
  • Pruritus
  • Psoriasis
  • Raynaud's Syndrome
  • Rheumatoid Arthritis
  • Seborrheic Dermatitis
  • Skin Cancer
  • Tendonitis
  • Tinea Versicolor
  • Wound Cleansing

Drug List:

fidaxomicin


fye-dax-oh-MYE-sin


Commonly used brand name(s)

In the U.S.


  • Dificid

Available Dosage Forms:


  • Tablet

Chemical Class: Macrolide


Uses For fidaxomicin


Fidaxomicin is used to treat adults with Clostridium difficile-associated diarrhea (CDAD).


Fidaxomicin belongs to the class of medicines known as macrolide antibiotics. It works by killing bacteria or preventing their growth. However, fidaxomicin will not work for colds, flu, or other virus infections.


fidaxomicin is available only with your doctor's prescription.


Before Using fidaxomicin


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For fidaxomicin, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to fidaxomicin or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of fidaxomicin in the pediatric population. Safety and efficacy have not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of fidaxomicin in the elderly.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of fidaxomicin. Make sure you tell your doctor if you have any other medical problems, especially:


  • Infection, systemic—Should not be used to treat systemic infections.

Proper Use of fidaxomicin


Take fidaxomicin only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.


You may take fidaxomicin with or without food.


To help clear up your infection completely, keep using fidaxomicin for the full time of treatment, even if you begin to feel better after a few days. If you stop using fidaxomicin too soon, your infection may return.


Dosing


The dose of fidaxomicin will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of fidaxomicin. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage form (tablets):
    • For Clostridium difficile-associated diarrhea (CDAD):
      • Adults—200 milligrams (mg) two times a day for 10 days.

      • Children—Use and dose must be determined by your doctor.



Missed Dose


If you miss a dose of fidaxomicin, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using fidaxomicin


It is very important that your doctor check your progress after you finish taking fidaxomicin. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it.


If your symptoms do not improve within a few days after you start fidaxomicin or if they become worse, check with your doctor.


Do not take any medicine to treat diarrhea without first checking with your doctor. Diarrhea medicines may make the diarrhea worse or make it last longer. If you have any questions about this or if mild diarrhea continues or gets worse, check with your doctor.


fidaxomicin Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


Less common
  • Abdominal or stomach pain

  • bloating

  • bloody or black, tarry stools

  • chills

  • confusion

  • constipation

  • cough

  • drowsiness

  • fever

  • loss of appetite

  • lower back or side pain

  • muscle tremors

  • nausea

  • painful or difficult urination

  • pale skin

  • rapid, deep breathing

  • restlessness

  • severe constipation

  • shortness of breath

  • sore throat

  • stomach cramps

  • troubled breathing with exertion

  • ulcers, sores, or white spots in the mouth

  • unusual bleeding or bruising

  • unusual tiredness or weakness

  • vomiting

  • vomiting of blood or material that looks like coffee grounds

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Less common
  • Abdominal or stomach distension or tenderness

  • acid or sour stomach

  • belching

  • blurred vision

  • difficulty with swallowing

  • dry mouth

  • excess air or gas in the stomach or intestines

  • flushed, dry skin

  • fruit-like breath odor

  • full feeling

  • heartburn

  • increased hunger

  • increased thirst

  • increased urination

  • indigestion

  • itching skin

  • passing gas

  • rash

  • stomach discomfort or upset

  • sweating

  • troubled breathing

  • unexplained weight loss

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: fidaxomicin side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More fidaxomicin resources


  • Fidaxomicin Side Effects (in more detail)
  • Fidaxomicin Dosage
  • Fidaxomicin Use in Pregnancy & Breastfeeding
  • Fidaxomicin Drug Interactions
  • Fidaxomicin Support Group
  • 0 Reviews for Fidaxomicin - Add your own review/rating


  • Fidaxomicin Professional Patient Advice (Wolters Kluwer)

  • Fidaxomicin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Dificid Prescribing Information (FDA)

  • Dificid Consumer Overview



Compare fidaxomicin with other medications


  • Clostridial Infection

Decapeptyl SR 11.25mg





Decapeptyl SR 11.25 mg for injection



triptorelin




Indication: Advanced Prostate Cancer



Information For The Patient


Please read this leaflet carefully. It provides some information about your medicine.


If you have any questions please ask your doctor. The name of your medicine is Decapeptyl SR 11.25 mg. Its active ingredient is triptorelin. Each vial contains 15 mg triptorelin (as acetate). There is an extra amount in the vial to make sure you receive the required dose of 11.25 mg. The formulation contains a lactide-glycolide copolymer, mannitol, polysorbate 80 and carmellose sodium.



Decapeptyl SR 11.25 mg is a powder for suspension for injection and the suspension will be made up with the suspension vehicle just before injection. The suspension vehicle contains mannitol in water.


This pack contains one vial of Decapeptyl SR 11.25 mg, one ampoule of suspension vehicle containing mannitol in water, one syringe and two needles. It is for single use only.




What is Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is a slow release formulation of triptorelin with an action lasting for 3 months. Triptorelin is a decapeptide, an analogue of GnRH. It lowers the levels of the male hormone testosterone in the body.


The instructions for preparing the injection are given overleaf. Your doctor or nurse will make up the injection and give it to you.




Who makes Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is manufactured by



Ipsen Pharma Biotech

Signes

France


The Product Licence holder is



Ipsen Ltd

190 Bath Road

Slough

Berkshire

SL1 3XE

UK




What is Decapeptyl SR 11.25 mg used for?


For the treatment of advanced prostate cancer.




Is there any reason for not being given Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg may not be suitable for you if you have experienced any of the following:


  • back pain or tingling ('pins and needles') in your hands and feet

  • if you had an allergic reaction to triptorelin, any other ingredients of Decapeptyl SR 11.25mg or to a similar type of drug (GnRH analogues)

Your doctor will know if the medicine is suitable for you. Consult your doctor if you are concerned.




Do I need to take any other medicines?


Your doctor may wish to give to you another medicine at the same time. This medicine will help to stop the increase in some symptoms which may occur at first. During the first month of therapy your doctor may want to monitor your condition carefully.




Tell your doctor if:


You think your symptoms have worsened or changed. Tell him if you are having more pain or if you are having difficulty in passing water. He will be able to decide if any changes are needed to your treatment. If you are taking any other medicines, tell your doctor about them.




How many injections will I need?


You will be given one injection every three months. Your doctor will decide for how long you need treatment.




Where will I be injected?


The injection will usually be given in your buttock.




What shall I do if I miss an injection?


As soon as you realise that you have missed an injection, contact your doctor. He will then be able to give you your next injection.




What will happen if I stop taking Decapeptyl SR 11.25 mg?


You may experience a worsening of your symptoms such as more pain, hot flushes, difficulty in passing water.




Which side effects can Decapeptyl SR 11.25 mg have?



Prostate cancer:
Decapeptyl SR 11.25 mg can cause unwanted side effects such as hot flushes, impotence, less desire for sex, bone pain, back pain, numbness or tingling sensations in lower limbs, pain or difficulty in passing water. These effects usually occur during the first month of treatment.


Less common side effects are temporary increase of blood pressure, breast enlargement, sleeplessness, changes in mood or personality, vertigo and dizziness.


The following side effects have been observed rarely: allergic reactions (rash, inflammation and itching), dry mouth or watering mouth, inflammation of veins, headache, recurrence of asthma, fever, sweating, stomach ache, feeling or being sick, weight gain, slight hair loss, blurred or abnormal vision and pain/hardened tissue at the injection site.


If any side effect is troublesome, or causes you concern, you should tell your doctor.




Further information


Keep your medicine out of the reach and sight of children.


Do not store above 25ÂșC and keep the container in the outer carton, to protect from light.


Do not use after the expiry date shown on the box.




Date of the last revision of this leaflet


November 2009.




Product Licence Numbers



Decapeptyl SR 11.25 mg PL Number: 06958/0016.


Suspension vehicle PL Number: 06958/0019.


Decapeptyl is a registered trademark.





Indication: Endometriosis



Information For The Patient


Please read this leaflet carefully. It provides some information about your medicine.


If you have any questions please ask your doctor. The name of your medicine is Decapeptyl SR 11.25 mg. Its active ingredient is triptorelin. Each vial contains 15 mg triptorelin (as acetate). There is an extra amount in the vial to make sure you receive the required dose of 11.25 mg. The formulation contains a lactide-glycolide copolymer, mannitol, polysorbate 80 and carmellose sodium. Decapeptyl SR 11.25 mg is a powder for suspension for injection and the suspension will be made up with the suspension vehicle just before injection. The suspension vehicle contains mannitol in water.


This pack contains one vial of Decapeptyl SR 11.25 mg, one ampoule of suspension vehicle containing mannitol in water, one syringe and two needles. It is for single use only.




What is Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is a slow release formulation of triptorelin with an action lasting over 3 months. Triptorelin is a decapeptide, an analogue of GnRH. It lowers the levels of the oestrogens and progesterone in the body.


The instructions for preparing the injection are given overleaf. Your doctor or nurse will make up the injection and give it to you.




Who makes Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is manufactured by



Ipsen Pharma Biotech

Signes

France


The Product Licence holder is



Ipsen Ltd

190 Bath Road

Slough

Berkshire

SL1 3XE

UK




What is Decapeptyl SR 11.25 mg used for?



Decapeptyl SR 11.25 mg is used for the treatment of endometriosis.




Is there any reason for not being given Decapeptyl SR 11.25 mg?


You should not be given Decapeptyl SR 11.25 mg if you are pregnant, trying to become pregnant, or breastfeeding. Decapeptyl SR 11.25 mg may not be suitable for you if you are suffering from a disease which affects the strength of your bones. Also, it may not be suitable for you if you have had an allergic reaction to triptorelin, to any of the ingredients of Decapeptyl SR 11.25 mg or to a similar type of drug (GnRH analogues). Your doctor will know if the medicine is suitable for you. Consult your doctor if you are concerned.




Do I need to take any other medicines?


During the course of your treatment with Decapeptyl SR 11.25 mg, and for at least 3 months after the last injection, your doctor may recommend you use a barrier method of contraception such as the condom or diaphragm (cap). This will ensure that you do not become pregnant whilst being treated with Decapeptyl SR 11.25 mg. Oral contraceptives (the 'pill') should not be taken when receiving Decapeptyl SR 11.25 mg. Your doctor may wish to give you additional treatment to reduce thinning of the bones. During the first month of therapy your doctor may want to monitor your condition carefully.




Tell your doctor if:


You think your symptoms have worsened or changed. Tell him if you have an abnormal bleed during your course of treatment. He will be able to decide if changes are needed to your treatment. If you are taking any other medicines, tell your doctor about them.




How many injections will I need?


You will be given one injection every three months for up to six months. Only one course of treatment with Decapeptyl SR 11.25 mg (two injections) should be given.




Where will I be injected?


The injection will usually be given in your buttock.




What shall I do if I miss an injection?


As soon as you realise that you have missed an injection, contact your doctor. He will then be able to give you your next injection.




What will happen if I stop taking Decapeptyl SR 11.25 mg?


You may experience a return of your symptoms such as painful periods and pain during sexual intercourse.




Which side effects can Decapeptyl SR 11.25 mg have?


At the start of treatment, you may experience a worsening of symptoms (pelvic pain, painful periods) even though the treatment is producing a favourable effect. These symptoms normally disappear after the first or second week.


The most common side effects during treatment are hot flushes, sweating, vaginal dryness, less desire for sex, painful intercourse and irregular menstrual bleeding during the first month of treatment. After stopping treatment it may be some time before your periods return. You may also have sleeplessness, headaches or mood changes. Temporary pain, reddening or swelling at the injection site may occur.


Other less common side effects which may occur include breast pain, muscle cramps, painful joints, weight gain, feeling or being sick, stomach pain or discomfort, feelings of weakness, temporary increase of blood pressure, blurred or abnormal vision, rash, swelling, slight hair loss.


This type of medicine can cause a small loss of calcium from the bones (thinning of the bones). A partial recovery of this loss may occur when treatment is stopped.


If any side effect is troublesome, or causes you concern, you should tell your doctor.




Further information


Keep your medicine out of the reach and sight of children.


Do not store above 25ÂșC and keep the container in the outer carton, to protect from light.


Do not use after the expiry date shown on the box.




Date of the last revision of this leaflet


November 2009.




Product Licence Numbers



Decapeptyl SR 11.25 mg PL Number: 06958/0016.


Suspension vehicle PL Number: 06958/0019.


Decapeptyl is a registered trademark.





Indication: Precocious Puberty



Information For The Patient


Please read this leaflet carefully. It provides some information about your medicine.


If you have any questions please ask your doctor. The name of your medicine is Decapeptyl SR 11.25 mg. Its active ingredient is triptorelin. Each vial contains 15 mg triptorelin (as acetate). There is an extra amount in the vial to make sure you receive the required dose of 11.25 mg. The formulation contains a lactide-glycolide copolymer, mannitol, polysorbate 80 and carmellose sodium.



Decapeptyl SR 11.25 mg is a powder for suspension for injection and the suspension will be made up with the suspension vehicle just before injection. The suspension vehicle contains mannitol in water.


This pack contains one vial of Decapeptyl SR 11.25 mg, one ampoule of suspension vehicle containing mannitol in water, one syringe and two needles. It is for single use only.




What is Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is a slow release formulation of triptorelin with an action lasting for 3 months. Triptorelin is a decapeptide, an analogue of GnRH. It lowers the levels of the hormone testosterone, oestrogens and progesterone in the body.


The instructions for preparing the injection are given overleaf. Your doctor or nurse will make up the injection and give it to you.




Who makes Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg is manufactured by



Ipsen Pharma Biotech

Signes

France


The Product Licence holder is



Ipsen Ltd

190 Bath Road

Slough

Berkshire

SL1 3XE

UK




What is Decapeptyl SR 11.25 mg used for?


For the treatment of precocious puberty (onset before 8 years in girls and 9 years in boys).




Is there any reason for not being given Decapeptyl SR 11.25 mg?



Decapeptyl SR 11.25 mg may not be suitable for you if you have experienced the following:


  • if you had an allergic reaction to triptorelin, any other ingredients of Decapeptyl SR 11.25 mg or to a similar type of drug (GnRH analogues).

Your doctor will know if the medicine is suitable for you. Consult your doctor if you are concerned.




How many injections will I need?


You will be given one injection every three months. Your doctor will decide for how long treatment should be continued.




Where will I be injected?


The injection will usually be given in your buttock.




What shall I do if I miss an injection?


As soon as you realise that you have missed an injection, contact your doctor. He will then be able to give you your next injection.




What will happen if I stop taking Decapeptyl SR 11.25 mg?


Secondary sexual characteristics will reappear. In girls, periods may occur.




Which side effects can Decapeptyl SR 11.25 mg have?



Precocious puberty: Mild to moderate withdrawal bleeding (common) may occur in girls in the first month of treatment. Additional common adverse reactions may be observed such as injection site reactions and pain in the joints.


The following rare reactions have been reported: allergic reactions, headache, weight gain, increased blood pressure, blurred or abnormal vision, gastrointestinal disorders including abdominal pain and vomiting, nose bleeding, feeling unwell, muscle pain, mood disorders and nervousness.


If any side effect is troublesome, or causes you concern, you should tell your doctor. If you notice any side effects not mentioned in this leaflet, please inform your doctor or pharmacist.




Further information


Keep your medicine out of the reach and sight of children.


Do not store above 25ÂșC and keep the container in the outer carton, to protect from light.


Do not use after the expiry date shown on the box.




Date of the last revision of this leaflet


November 2009.




Product Licence Numbers



Decapeptyl SR 11.25 mg PL Number: 06958/0016.


Suspension vehicle PL Number: 06958/0019.


Decapeptyl is a registered trademark.








Thursday, April 5, 2012

Antihistamines


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Antihistamines are drugs that inhibit the action of histamine in the body by blocking the receptors of histamine. There are two types of histamine receptors H1 and H2. When H1 receptors are stimulated by histamine it may produce allergic reactions such as itching, hay fever and rash or hives.


Antihistamines treat the symptoms of allergic reactions. Some antihistamines are sedating and although some are classed as non-sedating antihistamines, they may still cause drowsiness in some people.

See also

Medical conditions associated with antihistamines:

  • Allergic Reactions
  • Allergic Urticaria
  • Allergies
  • Anaphylaxis
  • Anorexia
  • Anorexia Nervosa
  • Anxiety
  • Cluster Headaches
  • Cold Symptoms
  • Conjunctivitis, Allergic
  • Cough
  • Cushing's Syndrome
  • Dermatographism
  • Extrapyramidal Reaction
  • Eye Dryness/Redness
  • Eye Redness/Itching
  • Failure to Thrive
  • Hay Fever
  • Insomnia
  • Interstitial Cystitis
  • Light Sedation
  • Migraine
  • Motion Sickness
  • Nasal Congestion
  • Nausea/Vomiting
  • Opiate Adjunct
  • Pain
  • Pruritus
  • Rhinorrhea
  • Sedation
  • Sexual Dysfunction, SSRI Induced
  • Upper Respiratory Tract Infection
  • Urticaria
  • Vasomotor Rhinitis
  • Vertigo

Drug List:

Tuesday, April 3, 2012

Synthetic ovulation stimulants


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Synthetic ovulation stimulants are drugs that stimulate ovulation or release of ovum from the ovaries.


The drug in this category has a similar structure to estrogen. It binds to the estrogen receptors so the brain thinks there is a low level of estrogen in the body. Therefore estrogen cannot provide accurate negative feedback to the hypothalamus and gonadotropin releasing hormone (GnRH) is released. GnRH activates the pituitary gland to release follicle stimulating hormone (FSH) and luteinizing hormone (LH). FSH and LH secretion stimulates growth of ovarian follicles and subsequent release of the egg.


Synthetic ovulation stimulants are used in treating infertility in anovulatory women.

See also

Medical conditions associated with synthetic ovulation stimulants:

  • Female Infertility
  • Lactation Suppression
  • Oligospermia
  • Ovulation Induction

Drug List:

Sunday, April 1, 2012

Ophthalmic antihistamines and decongestants


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Ophthalmic antihistamines and decongestants are products designed especially so that it can be applied in the eyes to treat hay fever symptoms such as runny eyes and redness.


Antihistamines block the histamine receptors and inhibit the action of histamine, which when activated cause runny eyes, redness, itching and so on. Decongestants are sympathomimetic drugs that relieve redness in the eyes.

See also

Medical conditions associated with ophthalmic antihistamines and decongestants:

  • Conjunctivitis
  • Conjunctivitis, Allergic
  • Eye Dryness/Redness
  • Eye Redness/Itching
  • Keratitis
  • Keratoconjunctivitis
  • Pupillary Dilation
  • Seasonal Allergic Conjunctivitis

Drug List: