Klonopin Withdrawal.
Klonopin withdrawal step by step
procedure. Klonopin withdrawal. Withdrawal from Klonopin no
longer needs to be grueling and suffering from the Klonopin
withdrawal side effects can be a thing of the past. You are
now on The Road Back web site, we are a non-profit, located
in the United States, offer assistance for free and most
importantly we show you what you can do right now for
Klonopin withdrawal without the need to purchase a book.
Klonopin Withdrawal
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.
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.
The web site
you are on now, The Road Back, offers information on
how to get off Klonopin and reduce Klonopin
withdrawal side effects. Many of you taking Klonopin
were prescribed Klonopin for anxiety, general
anxiety disorder, panic attacks, and possibly for
other reasons.
The Road Back
is a member of California Association of Alcoholism & Drug
Abuse Counselors (CAADAC). Since 1999, The Road Back has
helped thousands of people off Klonopin and has helped as many people that
wanted to stay on Klonopin reduce the side effects of taking
this medication. The Road Back is the largest outpatient
drug withdrawal program in the world. We are based in the
United States, with additional locations in Europe and the
United Kingdom.
Spend a minute or two and read an e-mail we received
November 10, 2014.
“Jim, here is my
testimonial. Feel free to use however you wish.
God bless you! WARNING: KLONIPIN IS A VERY ADDICTIVE
AND DANGEROUS DRUG SIDE EFFECTS can be serious
and harmful to overall health. WITHDRAWAL from this
drug is dangerous and might very well kill you
This is what any physician should be
required to advise patients upon prescribing Klonopin. I
began my journey to Hell a little over 6 years ago while
going through a nasty divorce. I was experiencing
major anxiety, panic attacks, and insomnia. These
symptoms did improve. However, over the years I
developed hypertension and steadily gained weight which I
had never had a problem with. I began taking
Lisinopril for the hypertension.
I made the decision to go off of the
Klonopin after seeing my gynecologist and discussing these
issues with her. She said that she felt the K was the
culprit. I asked how to taper, she told me to talk to
my family doctor who prescribed it to me. I was not
told of the horrible withdrawal so I didn't think it would
be a big deal. I began tapering....and did a complete
taper within a month. I had been taking 1 mg 3X daily
for 6+ years.
At first I did not attribute my
symptoms to the withdrawal. It was subtle at first,
smells and the taste of food was very strange. Hands
and feet numb and tingling. Unable to carry a train of
thought and to complete a task. I googled withdrawal
from Klonopin. I was shocked at what I read. I
prayed that I would not experience any of it.....and really
did not think this would happen to "me". Little did I
know that I had just begun my descent into Hell.
I do not feel that I can adequately
convey the nightmare. You just about have to go
through it to know what it is like. There are exceptions, as
Jim is proof of. I thank God for his dedication to
overcoming addiction and The Road Back. I will get
into this a little later.
Here is a list of what I experienced,
not in order and not to the degree of each symptom, there is
really no way to do so: major anxiety and panic attacks,
insomnia, hot/cold spells, severe sweating, no appetite,
sensitivity to noise/ light/ movement, pain in extremities,
blurred vision, ringing in ears, fullness in head,
vertigo, high bp even on lisinopril, increased heart rate,
confusion, disorientation, de-realization,
depersonalization, detachment. I was completely unable
to function.
About two weeks into this horror, my
daughter visited and started researching online. She
found The Road
Back program. I was willing to try
anything. My husband placed an order for the Neuro
Endure Mini. Of course it would be a few days to
receive it which doesn't seem long. But when you are
living a minute to minute nightmare it is a very long time.
And I was not certain it would even work. I was at the
end of my rope. I had not slept in 4 consecutive days
and nights. My heart rate was 130+ constantly. I
felt like I was going to die. My husband thought that
since I had read about these withdrawal symptoms that
somehow I should miraculously be "alright", bc it was
"normal" and I would eventually be okay. He told me to
"get a grip". I began to cry, uncontrollably.
And scream...it seemed as though it was not even coming from
me. I did not even feel human, I felt like an alien.
I could not take anymore.
My husband drove me to the ER. I
was terrified that I would be committed to the psyche ward.
I feared that the doctor would not understand (who
could???)! Thankfully I was wrong. After I had
somehow been talking for quite some time, he finally looked
me in the eye. I did not think I had gotten through to
him. He disclosed that his son had been addicted to K
and was hospitalized for seizures. I was relieved and
terrified at the same time. He reassured me that I was
most likely past the seizure stage. He said that
kicking the K would be the hardest thing I have ever done in
my life but that it would be so worth it. He did ask
me if I wanted to go back on the K, that the majority of ppl
could not make it through withdrawal and went back on the
drug. I will admit that I had thought about it......I
somehow found the courage to say NO. He was concerned
about my bp which was 157/124 P132 upon entering hospital.
But he did not want to address it just yet as he felt is was
a result of withdrawal. He prescribed a 20 day of
Lunesta for sleep. I actually slept for the first time
in days. Thank God for this doctor.
I thought that maybe since I had gotten
some sleep that my symptoms would improve. I was
wrong. I thought about Neuro Endure Mini and began an
agonizing wait. I would sit outside and wait for the
delivery, afraid that I would miss it. I was a bit
skeptical as I had the misconception that anything that
wasn't prescribed by a doctor was worthless. But yet I was
desperate and this man Jim Harper really seemed to know his
stuff. I finally received my NEM and had to restrain
myself to only take the recommended amount.
I had corresponded with Jim/The Road
Back on occasion. This was my lifeline. He
suggested keeping a journal to monitor my reactions and I
did. I am very thankful for this as now that I am
better it is a little difficult for me to remember how
debilitated I really was.
After only a few days I increased to 2
capsules 3X daily. On about day five, I began to catch
glimpses of "Jill". Very brief but still........it was
a start. I also began taking the JNK 3 capsules daily,
as well as Omega 3, vitamin E and biotin. It was a
slow and steady progression at first, but praise God I am
happy to report that I am feeling human again. I have
control again! I know without a doubt that these
supplements work! It seems like years ago that I first
contacted Jim. Hard to believe it has only been about
three months. Most with this degree of withdrawal
report at least a year. I do not think I could have
endured that. Occasionally I have a bad day, and I
found that even 1 glass of wine would set me back. I
avoid all alcohol. My bp and heart rate have returned
to normal! I no longer take Lunesta and I am able to sleep.
I am enjoying the things that brought me joy years ago.
I am discovering new and exciting things about myself.
I want to encourage anyone going
through withdrawal to Klonopin or other Benzo drugs to give
The Road Back a try. The information and support is
FREE. The supplements saved my life. I read some
reviews about the supplements being expensive.
Hello???????? I would have paid anything to be better,
even rehab. The ER doctor told me that his son had
been to rehab several times to no avail. I cannot
confirm or deny rehab treatment as I have not had it.
But I can tell you that the supplements are a mere fraction
of the cost of rehab. I will continue with the NEM
until I feel that I am completely well.
I hope that my experience will help
others that find themselves in this hellish nightmare.
I could never thank Jim Harper enough. God bless him
and The Road Back program.”
Jill A/North Carolina
If you are
already reducing Klonopin we know you are looking for relief
from the Klonopin withdrawal side effects and you want
relief fast. If you have already stopped Klonopin, the need
of assistance is no different and relief needs to come
quickly for you. You are not alone with these feelings and
Klonopin withdrawal symptoms.
You can click
How to Start located on the top
navigation line and read all chapters of How
to Get Off Psychoactive Drugs Safely for free. You can even
send us an e-mail to
books@theroadbackprogram.com
and we will e-mail you a pdf copy of the book for free.
If you are outside of the United States or Canada
Click Here for
distributors in or near your country.
Clonazepam
Brand name (Klonopin and Rivotril)
Pharmacology
Anticonvulsant
Clonazepam's pharmacological profile is similar to other
anxiolytic/sedative benzodiazepines. Its basic
anticonvulsive properties are also similar to those of other
diazepines. Clonazepam is capable of suppressing the spike
and wave discharge in absence seizures (petit mal) and
decreasing the frequency, amplitude, duration and spread of
discharge in minor motor seizures.
Clonazepam is well absorbed orally with maximum blood
concentrations occurring in 1 to 2 hours. Clonazepam is
metabolized by the liver to inactive metabolites, which are
excreted mainly in the urine. Less than 0.5% of a dose is
excreted in the urine unchanged and from 9 to 27% of a dose
may be excreted in the feces. The half-life of the parent
compound varies from approximately 18 to 50 hours.
Indications
Alone or as an adjunct in the management of myoclonic and
akinetic seizures and petit mal variant (Lennox-Gastaut
syndrome). May also be of some value in patients with
absence spells (petit mal) who have failed to respond to
succinimides.
Up to nearly 33% of the patients in some studies have shown
a loss of anticonvulsant activity, often within the first 3
months of clonazepam administration. In some cases, dosage
adjustment may re-establish efficacy.
Contraindications
Significant liver disease, narrow angle glaucoma,
sensitivity to benzodiazepines.
Warnings
Pregnancy:
Recent reports indicate an association between the use of
anticonvulsant drugs and an elevated incidence of birth
defects in children born to epileptic women taking such
medication during pregnancy. The incidence of congenital
malformations in the general population is regarded to be
approximately 2%; in children of treated epileptic women
this incidence may be increased 2 to 3 fold. The increase is
largely due to specific defects, e.g., congenital
malformations of the heart, and cleft lip and/or palate.
Nevertheless, the great majority of mothers receiving
anticonvulsant medications deliver normal infants.
Data are more extensive with respect to phenytoin and
phenobarbital, but these drugs are also the most commonly
prescribed anticonvulsants. Some reports indicate a possible
similar association with the use of other anticonvulsants,
including trimethadione and paramethadione. However, the
possibility also exists that other factors, e.g., genetic
predisposition or the epileptic condition itself may
contribute to or may be mainly responsible for the higher
incidence of birth defects.
Anticonvulsants should not be discontinued in patients in
whom the drug is administered to prevent major seizures,
because of the strong possibility of precipitating status
epilepticus with attendant hypoxia and risk to both the
mother and the unborn child. With regard to drugs given for
minor seizures, the risk of discontinuing medication prior
to or during pregnancy should be weighed against the risk of
congenital defects in the particular case and with the
particular family history.
Epileptic women of childbearing age should be encouraged to
seek professional counsel and should report the onset of
pregnancy promptly to their physician. Where the necessity
for continued use of antiepileptic medication is in doubt,
appropriate consultation might be indicated.
In a reproductive study in rabbits, clonazepam
administration was associated with an increased incidence of
cleft palate and other anomalies at 2 dose concentrations.
Accordingly, clonazepam should be used in women of
childbearing potential only when the expected benefits to
the patient warrant the possible risk to a fetus.
Lactation:
Mothers receiving clonazepam should not breast feed their
infants.
Children:
Because of the possibility that adverse effects on childhood
physical or mental development could become apparent only
after years, a risk-benefit consideration of the long-term
use of clonazepam is important in pediatric patients.
Precautions
Although simultaneous administration of several
anticonvulsants may be considered with clonazepam, such
combined therapy may result in an increase of central
depressant adverse effects. In addition, the dosage of each
drug may be required to be adjusted to obtain the optimum
effect.
Abrupt withdrawal of clonazepam particularly in those
patients on long-term, high dose therapy, may precipitate
status epilepticus. Therefore, as with any other
anticonvulsants, gradual withdrawal is essential when
discontinuing clonazepam. While clonazepam is being
gradually withdrawn, the simultaneous substitution of
incremental doses of another anticonvulsant may be
indicated.
A paradoxical increase in seizure activity or the appearance
of new seizure types has occurred in a very few patients
during clonazepam treatment. When used in patients in whom
several different types of seizures coexist, clonazepam may
increase the incidence or precipitate the onset of
generalized tonic-clonic seizures (grand mal). These
phenomena may require the addition of appropriate
anticonvulsants or an increase in their dosages. The
concomitant use of valproic acid and clonazepam may produce
absence status.
Occupational Hazards:
Caution patients receiving clonazepam against engaging in
hazardous occupations requiring complete mental alertness,
such as operating machinery or driving a motor vehicle.
They also should be warned against the concomitant use of
alcohol and other CNS depressant drugs.
The CNS depressant action of benzodiazepines may be
potentiated by other drugs such as alcohol, narcotics,
barbiturates, nonbarbiturate hypnotics, anxiolytics,
phenothiazines, thioxanthene and butyrophenone antipsychotic
agents, MAO inhibitors and tricyclic antidepressants.
Benzodiazepines have produced habituation, dependence and
withdrawal symptoms similar to those noted with barbiturates
and alcohol. Therefore, patients who may be prone to
increasing the dose of drugs on their own initiative should
be under careful monitoring when receiving clonazepam.
Periodic liver function tests and blood counts are
recommended during long-term clonazepam therapy.
Clonazepam and its metabolites are excreted by the kidneys;
to avoid excessive accumulation, exercise caution in
administering the drug to patients with impaired renal
function.
Hypersecretion in the upper respiratory passages has at
times been a troublesome adverse reaction during clonazepam
therapy, especially in small mentally retarded children who
ordinarily have difficulty handling secretions. Treatment
with clonazepam should be instituted with caution in
patients with chronic respiratory diseases.
Adverse Effects
The most frequently occurring adverse reactions to
clonazepam are referable to CNS depression. Drowsiness
occurs in approximately 50% of patients and ataxia in
approximately 30%. In some cases, these may diminish with
time. Behaviour problems have been noted in approximately
25% of patients and increased salivation in 7%.
Others, listed by system, are:
CNS:
Alterations in behaviour, which have been variously reported
as aggressiveness, argumentative behaviour, hyperactivity,
agitation, depression, euphoria, irritability, forgetfulness
and confusion. These behavioural reactions are particularly
likely to occur in patients with a prior history of
psychiatric disturbances and are known to occur in patients
with chronic seizure disorders.
Other adverse reactions involving the CNS have included
nystagmus, unsteady gait, slurred speech, dysarthria,
vertigo, insomnia, and diplopia. Isolated reports of
akinesia, hemiparesis, tremor, hypotonia, headache and
choreiform movements have been received. Minor changes in
EEG patterns specifically low-voltage fast activity.
Gastrointestinal:
Increased salivation, nausea, vomiting, anorexia,
constipation, diarrhea, encopresis, dry mouth, increased
appetite, abdominal pain, hepatomegaly.
Genitourinary:
Rare instances of dysuria, nocturia, incontinence, urinary
retention, enuresis.
Integumentary:
Nonspecific erythematous, papular and maculopapular rashes,
swelling of the face and eyelids, urticaria, pruritus.
Hirsutism and hair loss have also been reported, but drug
relationship has not been established.
Musculoskeletal:
Muscle weakness, low back pain.
Respiratory:
Hypersecretion in the upper respiratory passages, rhinorrhea,
dyspnea, respiratory depression.
Hematopoietic:
Anemia, leukopenia (WBC below 4000/mm(3)), thrombocytopenia,
eosinophilia.
Liver function:
Slight, transient elevations of transaminase and alkaline
phosphatase.
Miscellaneous:
Palpitations, coated tongue, dehydration, fever,
lymphadenopathy, weight gain or loss, changes in libido,
gynecomastia, hallucinations, dysdiadochokinesis, coma,
aphonia.
Overdose
Symptoms:
The cardinal manifestations of overdosage are drowsiness and
confusion, reduced reflexes and coma. There are minimal
effects on respiration, pulse and blood pressure, unless the
overdosage is extreme. Patients have recovered from dosages
of up to 60 mg without special treatment. When the effects
of the drug overdosage begin to wear off, the patient
exhibits some jitteriness and over stimulation.
Treatment:
Gastric lavage may be beneficial if performed soon after
ingestion of clonazepam. Supportive measures should be
instituted as indicated: maintenance of an adequate airway,
i.v. fluids and monitoring of pulse, blood pressure and
respiration. CNS stimulants and vasopressors may be used if
necessary. Dialysis appears to be of no value.
Dosage
Must be determined individually according to clinical
response and tolerance and depends primarily on the
patient's age.
Children:
In order to minimize drowsiness, the initial dose for
infants and children (up to 10 years of age or 30 kg) should
be between 10 and 30 mcg/kg/day and should not exceed 50
mcg/kg/day given in 2 or 3 divided doses. Dosage should be
increased by no more than 250 to 500 mcg every third day
until a maintenance dose of 100 to 200 mcg/kg has been
reached, unless seizures are controlled or adverse effects
preclude further increase. Whenever possible, the daily dose
should be divided into 3 equal doses. If doses are not
equally divided, the larger dose should be given before
retiring.
Adults:
The initial adult dose should not exceed 1.5 mg/day divided
into 3 doses. Dosage may be increased in increments of 0.5
to 1 mg every 3 days until seizures are adequately
controlled or until adverse effects preclude any further
increase. Maintenance dosage must be individualized for each
patient depending upon response. A recommended adult
maintenance dose is 8 to 10 mg/day in 3 divided doses.
Dosages in excess of 20 mg/day should be administered with
caution.
The use of multiple anticonvulsants may result in an
increase of depressant adverse effects. This should be borne
in mind whenever clonazepam is added to an already existing
anticonvulsant regimen.
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