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Abilify (Aripiprazole)

Abilify Information

Abilify, also referred to as Aripiprazole, is utilised in therapies for people suffering from the psychotic disorder schizophrenia. 

It is also utilised for sustaining a stable state in patients who have experienced symptom relief while taking other anti-psychotic drugs and who have been under observation for cases of health deterioration for about 6 and a half months. Bipolar Disordersare another illness where Abilify is utilised for treatment. Bipolar Disorders are also referred to as manic-depression. Abilify is approved by the Food and Drug Administration. Abilify comes in the form of tablets and can be obtained solely on prescription.

Abilify Warnings

The medicationAbilify has not been tested or deliberated with individuals under 18 years of age. Individuals allergic to Abilify, Aripiprazole or any other component of the drug, cannot follow this treatment. When following Abilify treatment, it is essential that there is no intake of alcohol during the period of the treatment. Do not breast-feed your child during the Abilify treatment. If you are expecting or are planning to have a baby, please inform your doctor. If you have suffered from fits or convulsions in the past, you should once again inform your doctor. Patients who are following treatments to control their sugar level in the blood are not advised to take Abilify as it contains sugar. Patients suffering from demential symptoms (which may consist of fall in concentration, fall in memory power) should not take Abilify.

Inform your doctor if you have previously suffered from a stroke/heart attack or have heart complications.

You should inform your doctor if you are following any other treatments or if you are taking any other drugs, especially Tegretol (carbamazepine), Fluoxetine, Ketoconazole, drugs for treating high BP, Paroxetine or Quinidine. Abilify might interfere with effectiveness of these drugs and vice versa. Also, severe side effects may occur when taking Abilify and these drugs simultaneously.

Abilify Side Effects

Abilify side effects, or side effects when utilising any anti-psychotic drug, can be of a very severe nature. You should inform your doctor immediately if you feel you are experiencing any of the following side effects.

1. Hyperglycemia – please consult your doctor in situations where it is essential for you to control your blood sugar levels. There have been cases of coma and fatal cases where patients taking Abilify experienced a rise in their blood sugar levels.

2. TD (Tardive dyskinesia) – indications of Tardive dyskinesia are muscular tremors which are anomalous or cannot be controlled.

3. Increased risks of heart attack – research and examinations carried out with older patients suffering from dementia have shown that intake of Abilify increases the risks of suffering from a stroke or heart attack

4. Effects on the mind – Abilify can affect thought processes, decision-making and motoring skills. You should not drive or utilise any dangerous equipment while taking Abilify until you know to what extent the drug affects you.

5. Dysphagia – Utilizing Abilify might cause you to have difficulties to swallow. This is also referred to as dysphagia. These difficulties might lead to suffocation. In certain cases, patients might experience aspiration pneumonia.

6. NMS (Neuroleptic Malignant Syndrome) – indications of NMS are perspiration, a confused state of mind, a considerable rise in body temperature, stiff muscles, alterations in the BP, pulse and abnormal rhythm of the heartbeat.

NMS can cause complete loss of muscle usage and malfunctions of the kidney. It can also cause death.

More frequent side effects of Abilify are:

Debility, a condition of nausea, throwing up, swellings and irritations, nervousness, difficulties in falling asleep, bowel complications, giddiness, drowsiness, headaches and an agitated stateof mind.

You should take precautions and ensure that you are not dehydrated and keep your body temperature stable.

If you start thinking of committing suicide, please inform your doctor.

Abilify Overdose

Indications of an Abilify overdose may consist of drowsiness and throwing up. If you feel you have taken an overdose of Abilify, please get in touch with your doctor as soon as possible.

If it so happens that you forget to take an Abilify dosage, do so right after you have remembered. But if you remember this when it almost time for the next Abilifydosage, do not take the dosage you missed. Continue to follow your usual Abilify dosage program.

Do not take 2 dosages simultaneously.

Abilify Usage Guidelines

Abilify comes in the form of a substance and a tablet for oral use. Abilify should be taken once daily. The medication can be administered with or without meals. It is suggested that Abilify be taken at approximately a similar time everyday. Read the instructions on your prescription thoroughly. If you have doubts as to how to take Abilify, please contact your doctor.

For adults, the suggested Abilify dosage is of 10mg or 15mg to be taken daily. Usually, your doctor will wait for a period of 2 weeks before changing the dosage.

Abilify should be taken as instructed by the doctor. Do not change your dosage without consulting your doctor and do not discontinue usage even if there is an improvement in your condition. Abilify controls the symptoms of schizophrenia but is not a permanent cure.

Storing Abilify

The medication Abilify should be stored at room temperature.

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Anafranil (Clomipramine HCL)

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What is Generic Anafranil (Clomipramine HCL)?

Generic Anafranil (Clomipramine HCL) is a tricyclic antidepressant. It affects chemicals in the brain that may become unbalanced.Generic Anafranil(Clomipramine HCL) is used to treat symptoms of obsessive-compulsive disorder (OCD) such as recurrent thoughts or feelings and repetitive actions.Generic Anafranil (Clomipramine HCL) may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Generic Anafranil (Clomipramine HCL)?

Do not use this medication if you have recently had a heart attack, or if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Do not use Generic Anafranil(Clomipramine HCL) if you are allergic to it or to similar drugs such as amitriptyline (Elavil, Etrafon), amoxapine (Ascendin), desipramine (Norpramin), doxepin (Sinequan), imipramine (Janimine, Tofranil),nortriptyline (Pamelor), protriptyline (Vivactil), or trimipramine (Surmontil). 

You may have thoughts about suicide when you first start taking an antidepressant, especially if you are younger than 24 years old. Your doctor will need to check you at regular visits for at least the first 12 weeks of treatment.Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself. 

What should I discuss with my healthcare provider before taking Generic Anafranil (Clomipramine HCL)?

Do not use this medication if you are allergic to Generic Anafranil (Clomipramine HCL) or to similar drugs such as amitriptyline (Elavil, Etrafon), amoxapine (Ascendin), desipramine (Norpramin), doxepin (Sinequan), imipramine (Janimine, Tofranil), nortriptyline (Pamelor), protriptyline (Vivactil), or trimipramine (Surmontil). 

Do not use Generic Anafranil (Clomipramine HCL) if you have recently had a heart attack, or if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take Generic Anafranil (Clomipramine HCL) before the MAO inhibitor has cleared from your body. 

Before taking Generic Anafranil (Clomipramine HCL),

 tell your doctor if you are allergic to any drugs, or if you have:heart disease or a history of heart attack, stroke, or seizures;bipolar disorder (manic-depression), schizophrenia or other mental illness;kidney or liver disease; overactive thyroid or adrenal gland tumor (pheochromocytoma);glaucoma; orproblems with urination.If you have any of these conditions, you may not be able to use Generic Anafranil (Clomipramine HCL), or you may need a dosage adjustment or special tests during treatment.

You may have thoughts about suicide when you first start taking an antidepressant, especially if you are younger than 24 years old. Tell your doctor if you have worsening symptoms of depression or suicidal thoughts during the first several weeks of treatment, or whenever your dose is changed.Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits for at least the first 12 weeks of treatment.

How should I take Generic Anafranil (Clomipramine HCL)?

Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Your doctor may occasionally change your dose to make sure you get the best results from this medication. Follow the directions on your prescription label.Take Generic Anafranil (Clomipramine HCL) with food to reduce stomach upset. If you need to have any type of surgery, tell the surgeon ahead of time that you are taking Generic Anafranil (Clomipramine HCL). 

You may need to stop using the medicine for a short time.Do not stop using Generic Anafranil (Clomipramine HCL) without first talking to your doctor. You may need to use less and less before you stop the medication completely. It may take up to 4 weeks of using this medicine before your symptoms improve. For best results, keep using the medication as directed. Talk with your doctor if your symptoms do not improve after 4 weeks of treatment. 

Store Generic Anafranil (Clomipramine HCL) at room temperature away from moisture and heat. 

What happens if I miss a dose?

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Generic Anafranil (Clomipramine HCL) can be fatal. Symptoms may include fast or uneven heart rate, extreme drowsiness, confusion, agitation, vomiting, blurred vision, sweating, muscle stiffness, increased or decreased urination, swelling, shortness of breath, blue lips or fingernails, feeling light-headed, fainting, seizure (convulsions), or coma. 

What should I avoid while taking Generic Anafranil (Clomipramine HCL)?

Avoid drinking alcohol. It can cause dangerous side effects when taken together with Generic Anafranil (Clomipramine HCL). Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, medicine for seizures, or other antidepressants). They can add to sleepiness caused by Generic Anafranil (Clomipramine HCL).Grapefruit and grapefruit juice may interact with Generic Anafranil (Clomipramine HCL). 

Discuss the use of grapefruit products with your doctor before increasing or decreasing the amount of grapefruit products in your diet.Generic Anafranil (Clomipramine HCL) can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid exposure to sunlight or artificial UV rays (sunlamps or tanning beds). Generic Anafranil (Clomipramine HCL) can make your skin more sensitive to sunlight and sunburn may result. Use a sunscreen (minimum SPF 15) and wear protective clothing if you must be out in the sun. 

Side effects of Generic Anafranil (Clomipramine HCL) 

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.Call your doctor at once if you have any of these serious side effects: chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;sudden numbness or weakness, especially on one side of the body;sudden headache, confusion, problems with vision, speech, or balance;feeling light-headed, fainting;fever, confusion, muscle stiffness, sweating, fast or uneven heartbeats;pale skin, easy bruising or bleeding, unusual weakness; orurinating more than usual.

Less serious side effects may be more likely to occur, such as:

nausea, vomiting, stomach pain, loss of appetite, constipation or diarrhea;dry mouth, unpleasant taste;increased appetite, weight changes;feeling anxious, restless, dizzy, drowsy, or tired;blurred vision, trouble concentrating;sleep problems (insomnia), nightmares;blurred vision;increased sweating; ordecreased sex drive, impotence, or difficulty having an orgasm.

What other drugs will affect Generic Anafranil (Clomipramine HCL)?

If you are using any of these drugs, you may not be able to use Generic Anafranil (Clomipramine HCL), or you may need dosage adjustments or special tests during treatment.There are many other medicines that can interact with Generic Anafranil (Clomipramine HCL). Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor. Keep a list with you of all the medicines you use and show this list to any doctor or other healthcare provider who treats you.

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Mycin (Erythromycin)

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BENZAMYCIN GEL

Benzamycin Gel Information

Benzamycin Gel is an effective remedy for the severe forms of acne. A therapy with this medical product can be accompanied by a treatment trial with other acne medical products. This medicine is a mixture between a drying (keratolytic) agent and a macrolide antibiotic. Both these ingredients are well known for their antibacterial effect. Thus, a therapy with Benzamycin Gel is so effective due to its peeling, antibacterial and drying effects.

Benzamycin Gel Indications

Benzamycin Gel should be prescribed to individuals who present the signs of the most severe types of acne. Your personal health care provider will tell you whether you should use this medicine in combination with any other acne drugs.

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Benzamycin Gel Warnings

A therapy with this medicine (Benzamycin Gel) is not recommended in the case of patients who are suffering from an Allergic Reaction to any of the active components of this medicine. In order to check whether you are hypersensitive or not to some of the most important components of Benzamycin Gel, you might have to undergo a set of clinical evaluations (allergy tests). Patients who are suffering from any blood medical conditions, or from any type of liver problems, ought to avoid starting a therapy with this medicine. Your personal health care provider will have to look for an alternative therapy method in such cases, as Benzamycin Gel is not the best therapy option for them.

This medication has been designed for external use only. It is very important to use this drug only on the affected skin areas. If you accidentally happen to let a small amount of this medication come into direct contact with your eyes, with the inside of your mouth and / or nose, on your lips, and so on you should immediately rinse that area with plenty of water. This medicine (Benzamycin Gel) must not be applied on open wounds, lesions, sunburns, irritated skin areas, or broken skin. If you personal health care provider has advised you to complete your therapy with Benzamycin gel with an adjacent treatment trial with 

another acne medical product, we strongly advise you to wait for at least 60 minutes before you are allowed to apply the other medication. Most patients who have followed a therapy with this medicine stated that they were able to see the improvements that were due to their therapy after a month or even two months. However, if your symptoms have not improved at all after 3 months of therapy, we advise you to stop your treatment and seek your physician’s professional guidance.

We strongly recommend all patients who are interested in benefiting from the best potential effect of their therapy with Benzamycin Pak Gel, to apply only cosmetics that are water-based during their prophylaxis with this drug. Studies have shown that a prolonged therapy with this medicine increases the skin’s sensitivity to direct sunlight. In other words, patients who use this medicine on a regular basis are more prone to developing unwanted (and even severe) sunburns. We recommend all patients to take extra precautions measurements during their therapy with this medicine. Wearing protective clothing and using an effective sunscreen will protect you from an unwanted allergy to the sun.

The ingredients of this medicine (Benzamycin Gel)can lead to the appearance of unwanted bleaches. We strongly recommend all individuals who are using this product to avoid letting it come into direct contact with carpeting, fabrics or hair. The safety of Benzamycin Gel in the case of young children (patients under 12 years of age) has not been established. Ask a pediatrician for further advice regarding this matter. If you become pregnant during your therapy with this medicine you should alert your personal health care provider as soon as possible.

Benzamycin Gel Intake Guidelines

We advise you to wash your hands before applying Benzamycin Gel. Try using this medicine at regular time intervals. Ask your personal physician for further information. You should also try reading the medicine’s label. Some patients have found it quite helpful. Before applying your doses of this drug you should check to see if the medicine is not expired. Ask your pharmacist how to dispose of the unused drug.

Benzamycin Gel Dosage

Although the medicine’s pack should contain a set of detailed information about the proper dosage of Benzamycin Gel, we advise you to check the dosage instructions from the label with those of your personal physician.

Benzamycin Gel Overdose

If you feel that you might be suffering from an unwanted overdose with Benzamycin Gel, we suggest you seek professional medical care. Contact your local poison control centre as soon as you can.

Benzamycin Gel Missed Dose

A disruption in your regular Benzamycin Gel dosing schedule is not a worrying situation. In such cases you should simply use a dose of this drug as soon as you regain access to your pack.

Benzamycin Gel Side Effects

A therapy with Benzamycin Gel can lead to the appearance of: feeling of warmth; dryness; irritation; hives; peeling; itching; stinging; redness; swelling of the skin, and so on. Other severe side effects can include: excessive itching, burning, redness, extreme dryness; tenderness of the skin; severe irritation; skin sloughing, and so on.

Benzamycin Gel Drug Reactions

As very little of Benzamycin Gel is absorbed into the skin, drug interactions are unlikely to occur.

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Depakote DR (Divalproex sodium DR)

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What is Depakote DR (Divalproex sodium DR)?

Divalproex sodium affects chemicals in the body that may be involved in causing seizures.Divalproex sodium is used to treat various types of seizure disorders. Divalproex sodium is sometimes used together with other seizure medications.Divalproex sodium may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about Depakote DR (Divalproex sodium DR) ?

In rare cases, divalproex sodium has caused life-threatening liver failure, especially in children younger than 2 years old. Children may be at even greater risk for liver problems if they use more than one seizure medication, if they have a metabolic disorder, or if they have a brain disease causing mental impairment (such as Creutzfeldt-Jacob disease, Huntington disease, multiple sclerosis, or a brain injury or infection). 

Seek emergency medical attention if the person taking this medicine has nausea, vomiting, stomach pain, or loss of appetite, low fever, dark urine, clay-colored stools, or jaundice (yellowing of the skin or eyes). 

These symptoms may be early signs of liver damage. Some of these symptoms may also be early signs of pancreatitis. Divalproex sodium can cause birth defects. Do not use this medication without your doctor's consent if you are pregnant. Use an effective form of birth control, and tell your doctor if you become pregnant during treatment. 

You may have thoughts about suicide while taking this medication. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself. 

What should I discuss with my healthcare provider before taking Depakote DR (Divalproex sodium DR) ?

In rare cases, divalproex sodium has caused life-threatening liver failure, especially in children younger than 2 years old. Children of this age may be at even greater risk for liver problems if they use more than one seizure medication, if they have a metabolic disorder, or if they have a brain disease causing mental impairment (such as Creutzfeldt-Jacob disease, Huntington disease, multiple sclerosis, or a brain injury or infection). Divalproex sodium has also caused rare cases of life-threatening pancreatitis (inflammation of the pancreas). Pancreatitis can come on suddenly and symptoms may start even after you have been taking divalproex sodium for several years. Do not take divalproex sodium if you have liver disease or a urea cycle disorder. 

If you have any of these other conditions, you may need a dose adjustment or special tests to safely take divalproex sodium.a bleeding or blood clotting disorder;a history of head injury, brain disorder, or coma;a family history of a urea cycle disorder;a family history of infant deaths with unknown cause; orHIV or CMV (cytomegalovirus) infection.You may have thoughts about suicide while taking this medication. 

Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed.Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

How should I take Depakote DR (Divalproex sodium DR) ?

Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the instructions on your prescription label.Drink plenty of water while you are taking this medication. 

Your dose may need to be changed if you do not get enough fluids each day. To be sure this medication is not causing harmful effects, your liver function will need to be tested. It is important that you not miss any scheduled visits to your doctor.Do not stop taking the medication even if you feel better. It is important to take divalproex sodium regularly to prevent seizures from recurring. Get your prescription refilled before you run out of medicine completely. Call your doctor promptly if this medicine does not seem to be working as well in preventing your seizures. 

Do not crush, chew, break, or open a delayed-release or extended-release tablet or capsule. Swallow the pill whole. It is specially made to release medicine slowly in the body. Breaking or opening the pill would cause too much of the drug to be released at one time. You may open the divalproex sodium sprinkle capsule and sprinkle the medicine into a spoonful of pudding or applesauce to make swallowing easier. 

Swallow this mixture right away without chewing. Do not save the mixture for later use. Discard the empty capsule.Carry an ID card or wear a medical alert bracelet stating that you are taking divalproex sodium, in case of emergency. Any doctor, dentist, or emergency medical care provider who treats you should know that you are taking divalproex sodium. Store divalproex sodium at room temperature away from moisture and heat. 

What happens if I miss a dose?

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include sleepiness or drowsiness, shallow breathing, weak pulse, or loss of consciousness.

What should I avoid while taking Depakote DR (Divalproex sodium DR) ?

Avoid drinking alcohol, which can increase some of the side effects of divalproex sodium. Divalproex sodium can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid exposure to sunlight or artificial UV rays (sunlamps or tanning beds). Divalproex sodium can make your skin more sensitive to sunlight and sunburn may result. Use a sunscreen (minimum SPF 15) and wear protective clothing if you must be out in the sun. 

Side effects of Depakote DR (Divalproex sodium DR) 

Seek emergency medical attention if the person taking this medicine has nausea, vomiting, stomach pain, or loss of appetite, low fever, dark urine, clay-colored stools, or jaundice (yellowing of the skin or eyes). These symptoms may be early signs of liver damage. 

Some of these symptoms may also be early signs of pancreatitis. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. 

Call your doctor at once if you have any of these serious side effects: unexplained weakness with vomiting and confusion or fainting;easy bruising or bleeding, blood in your urine;fever, sore throat, and headache with a severe blistering, peeling, and red skin rash;fever, chills, body aches, flu symptoms;urinating less than usual;hallucinations (seeing things that aren't there);extreme drowsiness, lack of coordination; ordouble vision or back-and-forth movements of the eyes.Less serious side effects may include:mild drowsiness or weakness;diarrhea, constipation, upset stomach;depression, anxiety, or other emotional changes;changes in your menstrual periods;enlarged breasts;tremor (shaking);hair loss;weight changes;vision changes; orunusual or unpleasant taste in your mouth.

What other drugs will affect Depakote DR (Divalproex sodium DR) ?

Cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for depression or anxiety can add to sleepiness caused by divalproex sodium. Tell your doctor if you regularly use any of these medicines, or any other seizure medication.

Before taking divalproex sodium, tell your doctor if you are using any of the following drugs:topiramate (Topamax);tolbutamide (Orinase);a blood thinner such as warfarin (Coumadin);aspirin or acetaminophen (Tylenol);zidovudine (Retrovir);clozapine (Clozaril, FazaClo);diazepam (Valium);meropenem (Merrem);rifampin (Rifadin, Rimactane, Rifater); orethosuximide (Zarontin).

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