Wednesday, 30 December 2015

Zyloprim (Allopurinol)

Fast Escrow Refills Reviews 11:40 , , , , , , No comments :



Zyloprim is mostly prescribed to patients suffering from or prone to:

Zyloprim Information
Zyloprim, with the generic name of Allopurinol, works by repressing the production of uric acid in the body.
Zyloprim Indications
  • Gout
  • Increased levels of uric acid caused by cancer treatments
  • Kidney stones caused by high levels of uric acid
Have a talk with your physician before deciding to take Zyloprim especially if you have kidney or liver disease. You may be given a lower dosage or may need to undergo specific monitoring during the treatment period.
Zyloprim belongs to a class of drugs called FDA Pregnancy Category C. This entails that its effects to an unborn fetus is not certain. It is therefore suggested to see your doctor if you are pregnant before taking this drug.
Nursing mothers are also advised to consult their doctor prior to taking Zyloprim as this passes into breast milk and may be unsafe for the breastfeeding baby.


Zyloprim must be taken exactly as directed by your doctor. If there is any instruction in the label that appears unclear to you, ask your doctor, nurse, or pharmacist.

Each dose is taken with a full glass of water on a full stomach. To lessen the chance of kidney stone formations, it is recommended to drink 8 to 10 full glasses (8-ounce glasses) of fluid a day.
Unless directed by your doctor, Zyloprim must not be double dosed. If you miss a dose, take it as soon as you remember as long as it is not almost time for the next scheduled dose. Otherwise, forego missed dose and proceed with the next one.
If symptoms of over dosage are suspected, consult your doctor for the proper medical action.
Zyloprim Side Effects
Stop usage of Zyloprim and seek medical attention if you experience any of the following adverse conditions:
  • Allergic reactions such as difficulty in breathing, closing of the throat, swelling of the lips, tongue, face, or hives
  • Blood in the urine or painful urination
  • Rashes
  • Eye irritation
  • Fever, chills, or joint aches
  • Severe nausea or vomiting
Minor side effects that are more likely to occur include:
  • Upset stomach or diarrhea
  • Headache, dizziness or drowsiness
  • Acute attack of Gouty Arthritis
In any of the cases mentioned above, continue use of Zyloprim and inform your doctor. For other side effects not listed that are particularly causing discomfort or pain, tell your doctor right away.
Inform your doctor if you need to take ampicillin (Principen, Omnipen) or Amoxicillin (Amoxil, Augmentin, Trimox, Wymox) while under treatment with Zyloprim as this may likely result to having rashes. Also tell your doctor if you are taking Thiazide diuretics such as hydrochlorothiazide (Hydrodiuril, Hygroton, HCTZ), chlorothiazide (Diuril, others), chlorthalidone (Thalitone, others), orindapamide (Lozol). Diuretics may increase the amount of Zyloprim in the blood.
Other drugs may also have adverse interactions with Zyloprim, such as:
  • Azathioprine (Imuran)
  • Mercaptopurine (Purinethol)
  • Drugs used to cure cancer
  • Cyclosporine (Sandimmune, Neoral)
  • Chlorpropamide (Diabinese)
  • Warfarin (Coumadin)
  • Theophylline (Theochrone, Theolair, Theo-Dur)
If you are taking any of the above medications, inform your doctor. You may need to undergo special monitoring or may be given dosage adjustments.
Always have a talk with your doctor prior to taking other prescribed or over-the-counter medicines, including herbal products, while under treatment with Zyloprim.
Buy Zyloprim through our Online Pharmacy or at any Canada Pharmacy selling online prescriptions.
In some countries ZYLOPRIM may also be known as: Allopurinol, Alloprin, Alositol, Blemimol, Caplenal, Dabroson, Epidropal, Gichtex, Hexanurat, Miniplanor, Progout, Takanarumin, Xanturat, Zyloric, Alfadiman, Puritenk, Allohexal, Allosig, Capurate, Gewapurol, Alpuric, Docallopu, Labopurinol, Talol, Apurol, Milurit, Allo-Efeka, Allo, Allobeta, Unizuric, Xanurace, Zurim, Uriconorme, Allo-Urik 

Benuryl (Probenecid)

Fast Escrow Refills Reviews 11:37 , , , , , , No comments :
Benuryl is a drug bearing the generic name Probenecid. Benuryl reduces the amount of uric acid in the body by causing more uric acid to be passed out in your urine.


Benuryl Indications
Benuryl is used to treat gout and Gouty Arthritis. Benuryl is also used to increase the effectiveness of some antibiotics.
Other than those listed in this medication guide, Benuryl may also be used for other purposes not listed in this medical guide.
Before taking this medication, tell your doctor if you have:
  • Allergic reactions to Benuryl
  • Kidney disease
  • Poor kidney function
  • Kidney stones
  • Stomach ulcer
  • Blood problems
  • Salicylate therapy
You may require a lower dose or special monitoring during treatment or you may not be able to take Benuryl if you have any of the conditions listed above.
Benuryl is in the FDA pregnancy category B, meaning it is not expected to harm an unborn baby. If you are pregnant, do not take Benuryl without first talking to your doctor.
It is not known whether Benuryl will harm a nursing baby. Prior to taking Benuryl talk to your doctor if you are breast-feeding a baby.
Children younger than 2 years of age should be not approved of Benuryl for use.
Take each dose of Benuryl with a full glass of water. Drink at least 8 to 10 full glasses of fluid every day to reduce the risk of kidney stone formation unless your doctor tells you not to. Take Benuryl with food or with an antacid to lessen stomach upset. Consult your doctor if nausea, vomiting, or loss of appetite is severe or persistent.
Take Benuryl exactly as instructed by your doctor. Ask your pharmacist, nurse, or doctor to explain to you if you do not understand the directions on your prescription bottle.
Seek urgent medical attention.
Symptoms of a Benuryl overdose include:
  • Nausea
  • Vomiting
  • Seizures
  • Coma
  • Death
Take the missed dose as soon as you recall. Skip the dose you missed and take only your next regularly scheduled dose if it is almost time for your next dose. Do not take a double dose of Benuryl.
Stop taking Benuryl and seek emergency medical attention if you experience any of the following serious side effects:
  • Difficulty in breathing
  • Closing of your throat
  • Swelling of your lips, tongue, or face
  • Hives
  • Blood in your urine
  • Pain when you urinate
  • Rash
Less serious side effects may be more likely to occur. Continue to take Benuryl and talk to your doctor if you experience:
  • Mild nausea
  • Vomiting
  • Loss of appetite
  • Headache
  • Dizziness
  • Sore gums
  • Flushing
  • Acute Gouty Arthritis attack
Other side effects not listed here may also occur. Talk to your doctor if you suspect other side effects that seem unusual or especially troublesome to you.

Arthrexin (Indomethacin)

Fast Escrow Refills Reviews 11:30 , , , , 1 comment :
Arthrexin (Indomethacin)

Arthrexin Information

Arthrexin, with the generic name of Indomethacin, is a highly effective non-steroidal anti-inflammatory medicine with marked analgesic and antipyretic properties.

Arthrexin Indications

Arthrexin is specially formulated to treat conditions such as:
  • rheumatoid arthritis
  • Osteoarthritis
  • Degenerative joint disease of the hip
  • Ankylosing spondylitis
  • Acute Gouty Arthritis
  • Acute musculoskeletal disorders (such as bursitis, tendonitis, synovitis, tenosynovitis, capsulitis of the shoulder, sprains and strains)
  • Low back pain (lumbago)
  • Fever (as a short term adjustment to a specific therapy)
  • Inflammation, pain, trismus, and swelling following dental procedures
  • Inflammation, pain, and swelling following orthopaedic surgical procedures and non-surgical procedures associated with reduction and immobilization of fractures or dislocations
  • Pain and associated symptoms of primary dysmenorrhea

Arthrexin Warnings/Precautions

Have a talk with your doctor before deciding to take Arthrexin. Inform your doctor if you have any of the conditions below:
  • Hypersensitivity to any ingredient of Arthrexin
  • Acute asthma attacks
  • Urticaria
  • Rhinitis as precipitated by acetylsalicylic acid or other non-steroidal anti-inflammatory agents
  • Active peptic ulcer
  • Recurrent history of gastrointestinal ulceration
  • Proctitis or recent rectal bleeding
It may not be advisable to take Arthrexin if you are suffering from any of the above ailments.
Arthrexin belongs to a class of drugs known as FDA Pregnancy Category D. This entails that it may affect the development of an unborn fetus. In case you are pregnant or planning to be while under treatment with Arthrexin, inform your doctor immediately.
Arthrexin is known to pass into breast milk. Nursing mothers are therefore advised to see their doctor before taking this drug.
Necessary precautions are informed to elderly patients as they are more prone to having side effects.
This drug is not recommended for use by children below 2 years or age.

Arthrexin Intake Instructions

Arthrexin must be taken as directed by your doctor. If there is any instruction that appears unclear to you, ask your doctor, nurse, or pharmacist.
Recommended dosage is 50 mg to 200 mg daily in divided doses and is adjusted to the patient’s response or tolerability to the medicine.

Arthrexin Missed Dose

Unless directed by your doctor, Arthrexin must not be double dosed. If you happen to miss a dose, take it as soon as you remember as long as it is not almost time for the next scheduled dose. Otherwise, skip missed dose and proceed with the next.

Arthrexin Overdose

Over dosage to suppositories are rare. However, should you experience any of the symptoms below, seek medical help:
  • Nausea
  • Vomiting
  • Intense headache
  • Dizziness
  • Mental confusion
  • Disorientation or lethargy
  • Paresthesias
  • Numbness
  • convulsions

Arthrexin Side Effects

If you feel any of these adverse reactions, see you doctor immediately for the proper medical attention:

  • headache, dizziness, lightheadedness
  • depression, vertigo, and fatigue (including malaise and listlessness)
  • mental confusion, anxiety
  • syncope
  • drowsiness
  • convulsions
  • coma
  • peripheral neuropathy
  • muscle weakness or involuntary muscle movements
  • insomnia
  • psychic disturbances (such as depersonalization, psychotic episodes
  • paresthesis, dysarthria, aggravation of epilepsy and parkinsonism
  • nausea
  • anorexia
  • vomiting
  • epigastric distress
  • abdominal pain, constipation, or diarrhea
  • Ulcerative Colitis, Stomatitis, gastritis, flatulence, bleeding from the sigmoid colon, regional ileitis
  • jaundice and hepatitis (though very rare)
  • oedema, elevation of blood pressure, trachychardia, chest pain, arrhythmia, palpitations, hypotension, congestive heart failure, BUN elevation, haematuria
  • hypersensitivity reactions (such as pruritus, urticaria, angiitis, skin rashes, others)
  • haematologic reactions (such as leucopenia, petechiae or ecchymosis, others)
  • blurred vision, diplopia, orbital and periorbital pain
  • tinnitus, hearing disturbances and deafness (rare)
  • proteinuria, nephritic syndrome, interstitial nephritis, and renal insufficiency (including renal failure)
  • vaginal bleeding, hyperglycaemia, glycosuria, hperkalaemia, flushing and sweating, epistaxis, ulcerative Stomatitis, breast changes, or gynercomastia
  • for suppositories, effects include: tenesmus, proctitis, rectal bleeding, burning, pain, discomfort, itching
For other possible side effects not mentioned that are particularly causing discomfort, tell your doctor at once.

Arthrexin Drug Interactions

Inform your doctor if you are taking any of the medications below before deciding to take Atropine:
  • acetylsalicylic acid and other salicylates
  • diflunisal
  • anticoagulants
  • Probenecid
  • Methotrexate
  • cyclosporine
  • lithium
  • diuretics
  • digoxin
  • antihypertensive medications
  • phenylpropanolamine
Have a talk with your doctor before deciding to take other prescribed or over-the-counter medicines while under treatment with Arthrexin.

Buy Arthrexin

Buy Arthrexin through our Online Pharmacy or at any Canadian Pharmacy selling online prescriptions.
In some countries ARTHREXIN may also be known as: Agilex, IM 75, Indotex, Klonametacina, Arthrexin, Indocid PDA, Flexidin, Indo, Indocollyre, Indohexal, Indomelan, Indoptol, Liometacen, Luiflex, Ralicid, Dolcidium, Agilisin, Metacidil, Novo-Methacin, Nu-Indo, Flexono, Rhodacine, Elmetacin, Indobene, Chrono-Indocid, Vonum Cutan, Indo-paed, Indocolir, Indomet-ratiopharm, Mobilat Akut Indo, Rheubalmin Indo, Dolcispray, Fortathrine, Hastel, Itapredin, Reumacid, Reumadolor, Indocollirio, Catlep, Infree, Antalgin, Artaxol, Draxil, Indocarsil, Labymetacyn, Italon, Soltacina, Autritis, Methocaps, Nisaid, Aliviosin, Artrinovo, Flogoter, Indolgina, Indonilo, Neo Decabutin, Indono, Inflamate, Inthacine, Metindo, Satogesic, Cevimin 

Thursday, 10 December 2015

Keppra (levetiracetam)

Fast Escrow Refills Reviews 05:46 , , , , , , No comments :
Keppra is used to treat partial onset seizures in adults and children who are at least 1 month old.
It is also used to treat tonic-clonic seizures in adults and children who are at least 6 years old, and myoclonic seizures in adults and children who are at least 12 years old.



INSTRUCTIONS
Take Keppra exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Your doctor may occasionally change your dose to make sure you get the best results.

Keppra is usually taken twice per day. Take the medicine at the same time each day. You may take Keppra with or without food.

Measure liquid medicine with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.
Do not crush, chew, or break a controlled release, delayed-release, or extended-release tablet. Swallow it whole. Breaking the pill may cause too much of the drug to be released at one time.

Use Keppra regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.

Do not stop using Keppra without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using this medicine suddenly. You may need to use less and less before you stop the medication completely.

Seizures are often treated with a combination of different drugs. Use all medications as directed by your doctor. Read the medication guide or patient instructions provided with each medication. Do not change your doses or medication schedule without your doctor's advice. .

Wear a medical alert tag or carry an ID card stating that you take Keppra. Any medical care provider who treats you should know that you take seizure medication.

To be sure Keppra is not causing harmful effects, your kidney function may need to be tested. Visit your doctor regularly.
If you missed a dose - take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


DOSAGE
Important Administration Instructions

Keppra is given orally with or without food. The Keppra dosing regimen depends on the indication, age group, dosage form (tablets or oral solution), and renal function.

Prescribe the oral solution for pediatric patients with body weight ≤ 20 kg. Prescribe the oral solution or tablets for pediatric patients with body weight above 20 kg.

When using the oral solution in pediatric patients, dosing is weight-based (mg per kg) using a calibrated measuring device (not a household teaspoon or tablespoon).
Keppra tablets should be swallowed whole. Keppra tablets should not be chewed or crushed.
Pediatric Patients
·         1 Month To < 6 Months
Treatment should be initiated with a daily dose of 14 mg/kg in 2 divided doses (7 mg/kg twice daily). The daily dose should be increased every 2 weeks by increments of 14 mg/kg to the recommended daily dose of 42 mg/kg (21 mg/kg twice daily). In the clinical trial, the mean daily dose was 35 mg/kg in this age group. The effectiveness of lower doses has not been studied.
·         6 Months To < 4 Years
Treatment should be initiated with a daily dose of 20 mg/kg in 2 divided doses (10 mg/kg twice daily). The daily dose should be increased in 2 weeks by an increment of 20 mg/kg to the recommended daily dose of 50 mg/kg (25 mg/kg twice daily). If a patient cannot tolerate a daily dose of 50 mg/kg, the daily dose may be reduced. In the clinical trial, the mean daily dose was 47 mg/kg in this age group.
·         4 Years To < 16 Years
Treatment should be initiated with a daily dose of 20 mg/kg in 2 divided doses (10 mg/kg twice daily). The daily dose should be increased every 2 weeks by increments of 20 mg/kg to the recommended daily dose of 60 mg/kg (30 mg/kg twice daily). If a patient cannot tolerate a daily dose of 60 mg/kg, the daily dose may be reduced. In the clinical efficacy trial, the mean daily dose was 44 mg/kg. The maximum daily dose was 3000 mg/day.

For Keppra tablet dosing in pediatric patients weighing 20 to 40 kg, treatment should be initiated with a daily dose of 500 mg given as twice daily dosing (250 mg twice daily). The daily dose should be increased every 2 weeks by increments of 500 mg to a maximum recommended daily dose of 1500 mg (750 mg twice daily).

For Keppra tablet dosing in pediatric patients weighing more than 40 kg, treatment should be initiated with a daily dose of 1000 mg/day given as twice daily dosing (500 mg twice daily). The daily dose should be increased every 2 weeks by increments of 1000 mg/day to a maximum recommended daily dose of 3000 mg (1500 mg twice daily).


Partial Onset Seizures
Adults 16 Years And Older

In clinical trials, daily doses of 1000 mg, 2000 mg, and 3000 mg, given as twice-daily dosing were shown to be effective. Although in some studies there was a tendency toward greater response with higher dose [see Clinical Studies], a consistent increase in response with increased dose has not been shown.

Treatment should be initiated with a daily dose of 1000 mg/day, given as twice-daily dosing (500 mg twice daily). Additional dosing increments may be given (1000 mg/day additional every 2 weeks) to a maximum recommended daily dose of 3000 mg. Doses greater than 3000 mg/day have been used in open-label studies for periods of 6 months and longer. There is no evidence that doses greater than 3000 mg/day confer additional benefit.
Myoclonic Seizures In Patients 12 Years of Age and Older With Juvenile Myoclonic Epilepsy
Treatment should be initiated with a dose of 1000 mg/day, given as twice-daily dosing (500 mg twice daily). Dosage should be increased by 1000 mg/day every 2 weeks to the recommended daily dose of 3000 mg. The effectiveness of doses lower than 3000 mg/day has not been studied.


Primary Generalized Tonic-Clonic Seizures
Adults 16 Years And Older
Treatment should be initiated with a dose of 1000 mg/day, given as twice-daily dosing (500 mg twice daily). Dosage should be increased by 1000 mg/day every 2 weeks to the recommended daily dose of 3000 mg. The effectiveness of doses lower than 3000 mg/day has not been adequately studied.


Pediatric Patients Ages 6 To< 16 Years
Treatment should be initiated with a daily dose of 20 mg/kg in 2 divided doses (10 mg/kg twice daily). The daily dose should be increased every 2 weeks by increments of 20 mg/kg to the recommended daily dose of 60 mg/kg (30 mg/kg twice daily). The effectiveness of doses lower than 60 mg/kg/day has not been adequately studied. Patients with body weight ≤ 20 kg should be dosed with oral solution. Patients with body weight above 20 kg can be dosed with either tablets or oral solution. Only whole tablets should be administered.


Adult Patients With Impaired Renal Function
Keppra dosing must be individualized according to the patient's renal function status.
STORAGE
Store Keppra at room temperature away from moisture, heat, and light.
Side effects
·         Get emergency medical help if you have any of these signs of an allergic reaction to Keppra: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, irritable, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Call your doctor at once if you have a serious side effect such as:
·         hallucinations, unusual thoughts or behavior;
·         bruising, severe tingling, numbness, pain, muscle weakness;
·         feeling very weak or tired;
·         fever, chills, body aches, flu symptoms, sores in your mouth and throat;
·         problems with walking or movement;
·         the first sign of any skin rash, no matter how mild; or
·         severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.
Less serious Keppra side effects may include:
·          mild dizziness or drowsiness;
·         mild tired feeling;
·         loss of appetite; or
·         stuffy nose.
This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect.



Dilantin (phenytoin)

Fast Escrow Refills Reviews 05:44 , , , , , , No comments :
Dilantin (phenytoin)
Dilantin Information
Dilantin is approved for use as an anti-seizure medication (anticonvulsant), especially to prevent tonic-clonic (grand mal) seizures and complex partial seizures (psychomotor seizures). It may be used alone or with Phenobarbital or other anticonvulsants.



Dilantin Warnings
Dilantin can increase the metabolism (elimination) of many drugs, reducing their concentrations in the body. Drugs that may be affected include: digoxin, carbamazepine, clonazepam, corticosteroids (e.g.prednisone), cyclosporine, disopyramide, doxycycline, estrogens, felodipine, levodopa, lidocaine, methadone, mexiletine, oral contraceptives, paroxetine, quinidine, tacrolimus, theophylline, phenobarbital, and warfarin. Dilantin can interact with these drugs not only when it is added to therapy but also when it is discontinued. In the latter case, the concentration of the other drugs may increase. Dilantin's metabolism may be affected by other drugs. Drugs that can reduce the amount of Dilantin in the body include rifampin and phenobarbital. Drugs that increase Dilantin concentrations include Amiodarone, chloramphenicol,cimetidine, disulfiram, fluconazole, fluoxetine, isoniazid (INH), omeprazole, and paroxetine. Thus, measuring levels of Dilantin in the blood may be necessary when patients begin or discontinue other medications. There appears to an increased risk of malformations and birth defects in women taking Dilantin . Thus Dilantin should be used in pregnancy only if the physician feels that the potential benefit outweighs the risk. Dilantin is secreted into breast milk. Nursing is not recommended for persons taking Dilantin .

Dilantin Side effects
Many varied adverse effects can occur during Dilantin therapy including dizziness, drowsiness, difficulty focusing (vision), unsteady gate, tiredness, abnormal involuntary movements, nausea, vomiting, constipation, abdominal pain, and loss of appetite. Children and young adults can develop overgrowth of the gums during long-term therapy which requires regular treatment by a dentist. Good oral hygiene and gum massage may reduce the risk. Rashes can occur in between 1 in 20 and 1 in 10 persons; some may be severe. Also, dark coloration of the skin may develop Dilantin can produce unusual growth of hair in some patients. This reaction most commonly affects the arms and legs but can also affect the trunk and face; it may be irreversible. Various lymph node reactions have been reported with Dilantin therapy. Lymph nodes may swell up, sometimes painfully. Dilantin may cause serum glucose to rise. Thus, blood sugar should be monitored closely when Dilantin is administered to patients with diabetes. Dilantin can potentially injure the liver although this is an uncommon occurrence. Dilantin can cause the platelet or white blood cell counts to drop, increasing the risk of bleeding or infection, respectively. Dilantin also can cause anemia. Because it interferes with vitamin D metabolism, Dilantin can cause weakening of the bones (osteomalacia). Dilantin can cause sexual dysfunction including decreased libido, impotence, and priapism (painful, prolonged erections).


Dilantin Overdose
If overdose is suspected, contact your local poison control center or emergency room immediately.



Wednesday, 9 December 2015

Norpress (Nortriptyline)

Fast Escrow Refills Reviews 06:46 , , , , , , No comments :
Norpress Information
The active substance of Norpress, namely Nortriptyline Hydrochloride, belongs to the tricyclic antidepressants class of medication. Its mechanism of action consists of an alteration of the chemical imbalance that may appear in parts of the patient’s brain, an imbalance that causes several physical or emotional symptoms that affect the patient’s general health condition and quality of life. Norpress has a strong positive effect on correcting this imbalance thus effectively treating these symptoms.



Norpress Indications
Norpress is typically used for the treatment of patients that suffer from depression, as it effectively treats the symptoms of this affection and improves the patients’ general condition. Apart from that, Norpress may also be successfully employed as part of the smoking cessation therapy, as it helps fight the withdrawal effects and as such may aid patients who wish to quit smoking. There are other uses for this medicine that are not listed here. If your prescriber advises you to follow a therapy course with this medicine and you are not sure why, it is best to ask him or her for more information.


Norpress Warnings
Norpress may not be administered to children or adolescents, or to patients that have recently suffered from heart attack. Individuals that are allergic to any of the active or inactive substances in this drug, or to any other tricyclic antidepressants or patients that are following a treatment with MAO inhibitors may not start taking Norpress.
Other medical conditions may influence your ability to start a treatment with Norpress. You should seek the advice of your physician if you have any liver, heart or kidney disorders, seizure disorders such as epilepsy, if you have diabetes, glaucoma, or hyperthyroidism (or if you are taking any thyroid gland related medication). Patients that are pregnant or breastfeeding, patients that have sustained heavy brain damage or head trauma, patients with bipolar disorders or mania, heavy drinkers or suicidal patients may require special consideration before starting to take this drug. Electroshock therapy and medication such as stimulants or sedatives may also interfere with the possibility of starting a treatment with Norpress. You should inform your prescriber of any other medical condition you are suffering from before receiving a prescription for this pharmaceutical product.


Norpress Intake Guidelines
Your prescriber will provide you with a complete set of guidelines for taking Norpress in order to achieve the best results from the therapy. It is best that you closely follow the prescriber’s indications. If the intake guidelines you are provided differ from any of the following information, you should take the drug as advised by your doctor.
The Norpress tablets need to be taken whole, without crushing or chewing them. You may take them with food or with a full glass of water. In some situations, the prescriber may recommend you to use just half a tablet at a time – this is only possible for the 25 mg tablets. The smoking cessation treatment typically lasts for 3 to 6 months, while the treatment for depression may last much longer. You should continue taking the tablets for the full duration of the therapy, although you may experience an improvement in your condition much sooner. Do not stop taking this medicine without your prescriber’s consent.


Norpress Dosage
For smoking cessation, the usual starting Norpress dosage is of 25 mg per day increasing in time to a maximum of 75 mg to 100 mg per day. The treatment should begin two to four weeks before the date you actually stop smoking. If the drug is employed for the treatment of depression, the treatment usually consists of three to four daily intakes of 25 mg each. Elderly patients will receive a lower daily dose than the adult one, for example 25 to 50 mg. Your prescriber may advise you to use a different Norpress dose than stated above. In this case, you should take the medication dosage that you have been prescribed.


Norpress Overdose
An overdose with Norpress is often a severe condition and requires prompt medical attention. As such, if you think that you may have taken too much of the medicine you should immediately contact the local poisons center or call your personal health care professional. In severe cases you may need to go to the nearest clinic or hospital in order to receive emergency medical assistance.


Norpress Missed Dose
You should keep a strict intake schedule for your Norpress doses, as this may help reduce the chances of accidentally missing any intakes. However, if you happen to miss a dose of the medicine, it is best that you completely skip taking it. Do not attempt to make up for the missed dose by taking a larger dose of the medicine. It is recommended that you continue taking the medicine as regular, but you should inform your personal physician in order to determine if any corrective measures need to be taken.


Norpress Side Effects
Norpress may cause a number of severe adverse reactions such as fainting, fits and seizures, severe chest pain, suicidal thoughts or allergic reactions. If you experience any of these you should immediately stop taking the drug and contact a trained health care professional. Other serious side effects of this medicine include jaundice, vision disturbances, heart beat disorders, hallucinations or confusion, anxiety, agitation or a worsening of the depression. You should inform your personal physician of these and any other unwanted effects that may appear during your Norpress treatment.


Norpress Drug Reactions
Norpress may cause accidental drug reactions with other antidepressants (either tricyclic antidepressants, MAO inhibitors or SSR inhibitors), blood pressure medication, anticholinergics, sympathomimetics, thyroid medications, some heart drugs, Carbamazepine or Cimetidine. You should inform your prescriber of any other pharmaceutical products you are taking before starting your Norpress therapy.



Subscribe to: Posts ( Atom )