Elavil withdrawal. The most successful Elavil
withdrawal program in the world. Elavil withdrawal.
The web site you are on now, The Road Back, offers
information on how to get off Elavil, prevent Elavil
withdrawal side effects as well as eliminating
current Elavil side effects.
Elavil Withdrawal
Head symptoms? Anxiety? Insomnia? Of course you do.
You likely would prefer to cut to the chase and find
out what you can do to get relief quickly. Omega 3
Supreme TG has been formulated to help cut through
the head symptoms quickly.
Neuro Day is formulated for the daytime anxiety and
most other daytime side effects
Neuro Night for sleep and body aches
JNK Formula helps bring a gene back to balance the
medication has altered.
Go to the manufacturers web site
Click here and purchase JNK
Formula, Neuro Day and Neuro Night and then get a
couple bottles of the Omega 3 Supreme. You will
be needing the extra omega's.
The web site
you are on now, The Road Back, offers information on
how to get off Elavil, prevent Elavil withdrawal
side effects as well as eliminating current Elavil
side effects.
You will find
on this site the complete book, How to Get Off
Psychoactive Drugs Safely. Click How to
Start, located on the top navigation menu
for book. Since 1999, over
50,000 people have now used this information to get
off their antidepressant or other type of
psychoactive medication.
Withdrawal off
of Elavil does not have to be difficult and handling
current Elavil side effects can be resolved quickly.
Note: If you are taking Elavil as well as an anti-anxiety medication
(benzodiazepine), the anti-anxiety medication must
be discontinued first. If you are only discontinuing
the Elavil the Elavil must be reduced very slowly to
prevent withdrawal side effects from the
anti-anxiety drug. Elavil slows the metabolism rate
of anti-anxiety drugs and when the Elavil is removed
from the system the anti-anxiety medication will not
take as long to metabolize and this creates a
withdrawal effect from the anti-anxiety medication.
See chapter 9 on the left side of each page for
anti-anxiety medication procedures.
In May 2012,
our program made its next leap forward and at this
time; completely eliminating Elavil side effects is
not only within our grasp, it is here.
Anxiety in the
daytime, insomnia at night, the dreaded head
symptoms common with Elavil withdrawal can now be a
thing of the past.
There is quite
a bit of information on our web site and if the ill
effects from Elavil have you unable to read very
much text, we can make this very quick and simple.
These
supplements are manufactured and sold by
Neuro Genetic Solutions.
Amitriptyline
Brand name (Elavil and Endep)
Pharmacology
Antidepressant
Indications
In the drug management of depressive illness.
Amitriptyline may be used in depressive illness of psychotic
or endogenous nature and in selected patients with neurotic
depression. Endogenous depression is more likely to be
alleviated than are other depressive states. Amitriptyline,
because of its sedative action, is also of value in
alleviating the anxiety component of depression.
As with other tricyclic antidepressants, amitriptyline may
precipitate hypomanic episodes in patients with bipolar
depression. These drugs are not indicated in mild depressive
states and depressive reactions.
Contraindications
In patients who have shown prior hypersensitivity to it. It
should not be given concomitantly with a MAO inhibiting
compound. Hyperpyretic crises, severe convulsions, and
deaths have occurred in patients receiving tricyclic
antidepressant and MAO inhibiting drugs simultaneously. When
it is desired to substitute amitriptyline for a MAO
inhibitor, a minimum of 14 days should be allowed to elapse
after the latter is discontinued. Amitriptyline should then
be initiated cautiously with gradual increase in dosage
until optimum response is achieved.
This drug is not recommended for use during the acute
recovery phase following myocardial infarction and in the
presence of acute congestive heart failure.
See Pregnancy under
Warnings.
Warnings
Amitriptyline should be used with caution in patients with a
history of seizures, impaired liver function, a history of
hepatic damage or blood dyscrasias and, because of its
atropine-like action, in patients with a history of urinary
retention, or with narrow-angle glaucoma or increased
intraocular pressure. In patients with narrow-angle
glaucoma, even average doses may precipitate an attack.
There has been a report of fatal dysrhythmia occurring as
late as 56 hours after amitriptyline overdose.
Patients with cardiovascular disorders should be watched
closely. Tricyclic antidepressant drugs, including
amitriptyline, particularly when given in high doses, have
been reported to produce arrhythmias, sinus tachycardia, and
prolongation of the conduction time.
A few instances of unexpected deaths have been reported in
patients with cardiovascular disorders. Myocardial
infarction and stroke have also been reported with drugs of
this class. Therefore, these drugs should be used with
caution in patients with a history of cardiovascular
disease, such as myocardial infarction and congestive heart
failure.
Concurrent administration of amitriptyline and electroshock
therapy may increase the hazards of therapy. Such treatment
should be limited to patients for whom it is essential.
Close supervision is required when amitriptyline is given to
hyperthyroid patients or those receiving thyroid medication.
Occupational Hazards:
May impair mental and/or physical abilities required for
performance of hazardous tasks, such as operating machinery
or driving a motor vehicle.
Pregnancy:
There are no well-controlled studies in pregnant women;
therefore, in administering the drug to pregnant patients or
women who may become pregnant, the potential benefits must
be weighed against the possible hazards to mother and child.
Lactation:
Amitriptyline is detectable in breast milk. Because of the
potential for serious adverse reactions in infants from
amitriptyline, a decision should be made whether to
discontinue nursing or discontinue the drug.
Children:
In view of the lack of experience with the use of this drug
in the treatment of depression in children, amitriptyline is
not recommended for depressed patients under 12 years of
age.
Precautions
The potency of amitriptyline is such that addition of other
antidepressant drugs generally does not result in any
additional therapeutic benefit. Untoward reactions have been
reported after the combined use of antidepressant agents
having varying modes of activity. Accordingly, combined use
of amitriptyline and other antidepressant drugs should be
undertaken only with due recognition of the possibility of
potentiation and with a thorough knowledge of the
pharmacology of both drugs. There has been no reports of
untoward events when patients receiving amitriptyline were
changed immediately to protriptyline or vice versa.
When amitriptyline is used to treat the depressive component
of schizophrenia, activation or aggravation of existing
psychotic manifestation may occur. Likewise, manic
depressive patients may experience hypomanic or manic
episodes and hyperactive or agitated patients may become
overstimulated. Paranoid delusions, with or without
associated hostility, may be exaggerated. A reduction in
dose or discontinuation of amitriptyline may be indicated
and administration of a neuroleptic such as a phenothiazine,
be considered under these circumstances.
Seriously depressed patients should be carefully supervised.
The possibility of suicide in depressed patients remains
during treatment. Patients should not have access to large
quantities of this drug during treatment.
Discontinue the drug several days before elective surgery if
possible.
Drug Interactions:
Amitriptyline may block the antihypertensive action of
guanethidine or similarly acting compounds.
When amitriptyline is given with anticholinergic agents or
sympathomimetic drugs, including epinephrine combined with
local anesthetics, close supervision and careful adjustment
of dosage are required. Paralytic ileus may occur in
patients taking tricyclic antidepressants in combination
with anticholinergic-type drugs.
Since amitriptyline, in combination with anticholinergic
type drugs, may give rise to paralytic ileus, particularly
in elderly or hospitalized patients, appropriate measures
should be taken if constipation occurs in these patients.
Cimetidine is reported to reduce hepatic metabolism of
certain tricyclic antidepressants.
Caution is advised if patients receive large doses of
ethchlorvynol concurrently. Transient delirium has been
reported in patients who were treated with 1 g of
ethchlorvynol and 75 to 150 mg of amitriptyline.
Amitriptyline may enhance the response to alcohol and the
effects of barbiturates and other CNS depressants. Delirium
has been reported with concurrent administration of
amitriptyline and disulfiram.
Note:
Included in this listing which follows are a few adverse
reactions which have not been reported with this specific
drug. However, pharmacological similarities among the
tricyclic antidepressant drugs require that each of the
reactions be considered when amitriptyline is administered.
Behavioral:
Drowsiness, fatigue, activation of latent schizophrenia,
disorientation, confusional states, hallucinations,
delusions, hypomanic reactions, disturbed concentration,
nightmares, insomnia, restlessness, agitation, excitement,
jitteriness, anxiety, giddiness.
Neurological:
Epileptiform seizures, coma, dizziness, tremors, numbness,
tingling, paresthesias of the extremities, peripheral
neuropathy, headache, ataxia, alteration in EEG patterns,
extrapyramidal symptoms including abnormal involuntary
movements and tardive dyskinesia, dysarthria, tinnitus,
incoordination, and slurred speech.
Anticholinergic:
Urinary retention, dilatation of the urinary tract,
constipation, paralytic ileus, especially in the elderly,
hyperpyrexia, dry mouth, blurred vision, disturbance of
accommodation, increased intraocular pressure, precipitation
of latent glaucoma, aggravation of existing glaucoma, and
mydriasis.
Cardiovascular:
Quinidine-like effect and other non-specific ECG changes and
changes in AV conduction, prolonged conduction time,
asystole, hypotension, syncope, hypertension, palpitation,
arrhythmias, heart block, ventricular tachycardia,
fibrillation, myocardial infarction, stroke, unexpected
death in patients with cardiovascular disorders.
Hematologic:
Bone marrow depression, including agranulocytosis,
leukopenia, eosinophilia, purpura, thrombocytopenia.
Allergic:
Skin rash, urticaria, photosensitization, edema of the face
and tongue, itching.
Gastrointestinal:
Nausea, epigastric distress, heartburn, vomiting, hepatitis
(including altered liver function and jaundice), anorexia,
stomatitis, peculiar taste, diarrhea, parotid swelling,
black tongue may occur.
Endocrine:
Testicular swelling, gynecomastia and impotence in the male,
breast enlargement and galactorrhea in the female, increased
or decreased libido, elevation and lowering of blood sugar
levels, syndrome of inappropriate ADH (antidiuretic hormone)
secretion.
Miscellaneous:
Weakness, increased perspiration, edema, urinary frequency,
alopecia, increased appetite, weight gain, weight loss.
Withdrawal Symptoms:
Abrupt cessation of treatment after prolonged administration
may produce nausea, headache, and malaise. Gradual dosage
reduction has been reported to produce, within 2 weeks,
transient symptoms including irritability, restlessness, and
dream and sleep disturbance. These symptoms are not
indicative of addiction. Rare instances have been reported
of mania or hypomania occurring within 2 to 7 days following
cessation of chronic therapy with tricyclic antidepressants.
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