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Sanjin Group
Hunan Sanjin Pharmaceutical Co., Ltd. is the sole pharmaceutical
manufacturer which pass the GMP audit about Lamotrigine raw
material and it’s finished product in China at present,.It is
aproved by clinic study that the safety,efficacy and quanlity
for Sanjin Lamotrigine as well as the imported Lamotrigine
products,but the Sanjin Lamotrigine is much more cheap than
imported one. Sanjin Lamotrigine is complying with the BP
requestment.
We
would like to make full use of our technical advantage to
cooperate with you on the Lamotrigine raw material and it’s
finish product exportation.



The information below are for reference only!
Lamotrigine
Definition
Lamotrigine is an anticonvulsant medication used in the
treatment of epilepsy. Epilepsy is a neurological disorder in
which excessive surges of electrical energy are emitted in the
brain, causing seizures. Lamotrigine is usually reserved for
difficult-to-control seizures that have not responded to other
anticonvulsant medications. In psychiatry, lamotrigine is also
indicated in the treatment of bipolar disorder
(manic-depression).
Purpose
While lamotrigine controls seizures associated with epilepsy,
there is no known cure for the disorder. Although the precise
mechanism by which lamotrigine exerts its therapeutic effect is
unknown, lamotrigine is thought to act at sodium channels in the
neuron (nerve cell) to reduce the amount of excitatory
neurotransmitters that the nerve cell releases.
Neurotransmitters are chemicals that aid in the transfer of
nerve impulses from one nerve junction to the next. With
decreased levels of these neurotransmitters, the electrical
activity in the brain that triggers seizures is reduced.
In the treatment of bipolar disorders, lamotrigine's effect upon
neurochemicals stabilizes mood, preventing sudden,
unpredictable, and severe episodes of mania and depression.
Description
For the treatment of epilepsy-related seizures, lamotrigine may
be used alone or in combination with other anti-epileptic drugs
(AEDs) or anticonvulsants. In the United States, lamotrigine is
sold under the brand name Lamictal.
Recommended dosage
Lamotrigine is taken orally, in either tablet or chewable form.
Chewable tablets may be dispersed into a liquid solution,
according to the prescribing physician's instructions.
Lamotrigine is prescribed by physicians in varying daily
dosages, usually ranging 200–900 mg per day divided into two
doses.
Beginning any course of treatment that includes lamotrigine
requires a gradual dose-increasing regimen. The safety and
effectiveness of lamotrigine in children under age 18 have not
been proven; therefore, the drug is seldom used in children.
Adults typically take an initial dose for the first two weeks
that is slowly increased over time. It may take several weeks to
realize the full benefits of lamotrigine, especially in those
patients taking lamotrigine for the treatment of bipolar
disorders.
A double dose of lamotrigine should not be taken. If a dose is
missed, it should be taken as soon as possible. However, if it
is within four hours of the next dose, then the missed dose
should be skipped. When ending a course of treatment that
includes lamotrigine, physicians typically direct patients to
gradually taper down their daily dosages over a period of
several weeks. Stopping the medicine suddenly may severely alter
mood or cause seizures to occur, even in patients taking
lamotrigine for the treatment of bipolar disorders.
Precautions
A physician should be consulted before taking lamotrigine with
certain non-prescription medications. Patients should avoid
alcohol and CNS depressants (medications that make one drowsy or
tired, such as antihistimines, sleep medications, and some pain
medications), while taking lamotrigine. Lamotrigine can
exacerbate the side effects of alcohol and some other
medications. Alcohol may also increase the risk or frequency of
seizures.
Lamotrigine may not be suitable for persons with a history of
liver or kidney disease, depressed renal functital illness,
anemia, high blood pressure, angina (chest pain), or irregular
heartbeats and other heart problems. Before beginning treatment
with lamotrigine, patients should notify their physician if they
consume a large amount of alcohol, have a history of drug use,
are nursing, pregnant, or plan to become pregnant.
Lamotrigine's safety during pregnancy has not been established.
Persons taking lamotrigine (and other AEDs or anticonvulsants)
should be aware that many AEDs and anticonvulsants cause birth
defects. Patients who become pregnant while taking any AED or
anticonvulsants should contact their physician immediately.
Side effects
Lamotrigine is generally well tolerated. However, in some
patients, lamotrigine may produce some of the traditionally mild
side effects associated with anticonvulsants. Headache, nausea,
and unusual tiredness and weakness are the most frequently
reported side effects of anticonvulsants. Other possible side
effects that do not usually require medical attention include:
mild coordination problems
mild dizziness
abdominal pain
sinus pain
sleepiness or sleeplessness
diarrhea or constipation
heartburn or indigestion
aching joints and muscles or chills
unpleasant taste in mouth or dry mouth
Many of these side effects disappear or occur less frequently
during treatment as the body adjusts to the medication. However,
if any symptoms persist or become too uncomfortable, the
prescribing physician should be consulted.
Other, uncommon side effects of lamotrigine can be serious and
may indicate an allergic reaction. Severe and potentially
life-threatening rashes have occurred during treatment with
lamotrigine, occurring approximately once in every 1,000 persons
who take the drug. In the unusual event that this rash develops,
it normally occurs within the first eight weeks of treatment. A
patient taking lamotrigine who experiences any of the following
symptoms should contact a physician immediately:
rash or bluish patches on the skin
sores in the mouth or around the eyes
depression or suicidal thoughts
mood or mental changes, including excessive fear, anxiety,
hostility
general loss of motor skills
persistent lack of appetite
altered vision
difficulty breathing
chest pain or irregular heartbeat
faintness or loss of consciousness
persistent, severe headaches
persistent fever or pain
Interactions
Lamotrigine may have negative interactions with some antacids,
antihistamines, antidepressants, antibiotics, and monoamine
oxidase inhibitors (MAOIs). Other medications such as HIV
protease inhibitors (indinavir), ritonavir (Norvir), ipratropium
(Atrovent), isoniazid, phenobarbital (Luminal, Solfoton),
nefazodone, metronidazole, acetazolamide (Diamox), propranolol (Inderal),
rifampin (Rifadin, Rimactane), and warfarin may also adversely
react with lamotrigine. Oral contraceptives (birth control
pills) may decrease the amount of lamotrigine absorbed by the
body.
Lamotrigine may be used with other seizure prevention
medications, if advised by a physician.
Resources
BOOKS
Devinsky, Orrin, M. D., Epilepsy: Patient and Family Guide, 2nd
ed. Philadelphia: F. A. Davis Co., 2001.
Weaver, Donald F. Epilepsy and Seizures: Everything You Need to
Know. Toronto: Firefly Books, 2001.
OTHER
"Lamotrigine." Medline Plus. National Library of Medicine. May
6, 2004 (June 1, 2004). http://www.nlm.nih.gov/medlineplus/druginfo/uspdi/202786.html.
"Lamotrigine." Yale New Haven Health Service Drug Guide. May 6,
2004 (June 1, 2004). http://yalenewhavenhealth.org/library/healthguide/enus/drugguide/topic.asp?hwid=multumd03809a1.
ORGANIZATIONS
Epilepsy Foundation. 4351 Garden City Drive, Landover, MD
20785-7223. (800) 332-1000. http://www.epilepsyfoundation.org.
American Epilepsy Society. 342 North Main Street, West Hartford,
CT 06117-2507. http://www.aesnet.org.
Generic Name: lamotrigine
Drug Class And Mechanism: Lamotrigine is an oral drug that is
used for treating seizures. It is chemically unrelated to other
anti-seizure drugs. The precise mechanism by which lamotrigine
exerts its anti-seizure action is not known.
Prescription: yes
Generic Available: no
Storage: Tablets should be stored at room temperature, between
15 and 30°C (59-86°F).
Prescribed For: Lamotrigine is used in combination with other
anti-seizure drugs in the treatment of some types of seizures.
It also is used alone for treating partial seizures in patients
16 years and older when converting from the anti-epileptic drug
valproate.
Dosing: The initial dose of lamotrigine in patients not taking
valproicacid (Depakote) is 50 mg once daily for two weeks,
followed by 100 mg daily given in two divided doses for two
weeks. Thereafter, the usual maintenance dose is 300 to 500 mg
daily given in two divided doses. In patients taking valproic
acid, the initial dose of lamotrigine is 25 mg every other day
for two weeks, then 25 mg once daily for two weeks, slowly
increasing the dose (by 25 to 50 mg per day) every one to two
weeks) until a dose of 100 to 150 mg daily is reached. Standard
doses of lamotrigine are given twice daily.
Drug Interactions: Lamotrigine can interact with valproic acid.
When lamotrigine is begun in patients already receiving valproic
acid, the blood concentrations of valproic acid can decrease
over a 3-week period. This may result in loss of seizure
control. The risk of severe skin rash may be increased by
combining lamotrigine with valproic acid.
There may be a higher incidence of dizziness, double vision, and
blurred vision in patients receiving carbamazepine together with
lamotrigine. The mechanism of this interaction is unclear.
Pregnancy: Damage to the fetus has been shown in some but not
all pregnant animal species given lamotrigine. There have been
no good studies in pregnant women. Physicians may choose to
prescribe lamotrigine to pregnant women if they feel the benefit
outweighs the potential risk.
Nursing Mothers: Lamotrigine is secreted into human breast milk.
Because the effects on the infant are unknown, breast-feeding
while taking lamotrigine is not recommended.
Side Effects: Severe, life-threatening rashes have occurred with
lamotrigine. The risk in children (for whom lamotrigine is not
approved) is as high as 1 in 50 to 1 in 100 patients. Rash is
rare in adults, but the risk is increased if the dose is
increased faster than recommended or if patients also are taking
valproic acid. Nearly all reported rashes have occurred within 2
to 8 weeks of starting therapy. Patients taking lamotrigine
should report any rash to a physician immediately.
Related Links on MedicineNet.com
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