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Zoloft Description:
Sertraline hydrochloride is an orally administered selective serotonin reuptake
inhibitor (SSRI) antidepressant. It is prescribed for depression and a number
of anxiety disorders, including social anxiety disorder (SAD), post-traumatic
stress disorder (PTSD), panic disorder, obsessive-compulsive disorder (OCD),
and premenstrual dysphoric disorder (PMDD) in adults over age 18. As well,
it is approved for OCD in children and adolescents aged 6-17.
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The FDA approved the drug, manufactured by Pfizer, for depression in 1992,
for OCD in 1996, for PMDD in 2002, and for SAD in 2003.
Classification:
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SSRI
Clinical Pharmacology:
The mode of action of Zoloft is believed to be linked to its inhibition of
CNS neuronal uptake of serotonin. Clinical trials at relevant doses in humans
have demonstrated that sertraline blocks the uptake of serotonin into human
platelets.
The chronic use of sertraline was found in animals to down-regulate brain
norepinephrine receptors, as with other drugs for treating depressive
disorder (MDD). Sertraline does not inhibit monoamine oxidase.
Indications and Dosage:
Sertraline is indicated for the treatment of MDD in adults. The efficacy of
the drug in treating a major depressive episode was established in six- to
eight-week trials of adult outpatients whose diagnoses corresponded to the
DSM-III category of MDD.
A major depressive episode implies a prominent and relatively persistent depressed
or dysphoric mood that usually interferes with day-to-day functioning (nearly
every day for at least 2 weeks). An episode should include at least 4 of the
following symptoms: change in sleep habits, change in appetite, psychomotor
agitation or retardation, loss of interest in usual activities or decreased
sex drive, increased fatigue, feelings of worthlessness or guilt, slowed thinking
or impaired concentration, and suicidal thoughts or behavior.
The initial dose of Zoloft should be administered for MDD and OCD at a dose
of 50mg/day, once daily.
For panic disorder, PTSD and SAD, treatment should be initiated with a dose
of 25mg/day, once daily. After one week, the dose should be increased to 50mg/day,
once daily.
Patients not responding to 50mg/day may benefit from increases up to a maximum
of 200mg/day. Given the rapid elimination half-life of Zoloft (24 hours), changes
in dosage should not occur at intervals of less than 1 week.
In patients suffering from PMDD, initial treatment should begin with a dose
of 50mg/day, either daily throughout the menstrual cycle or limited to the
luteal phase of the cycle, depending on the doctor’s assessment. Those
not responding to the 50mg/day treatment, benefit may be seen with increases
(at 50mg increments/menstrual cycle) up to 150mg/day when dosing throughout
the menstrual cycle, or 100mg/day when dosing during the luteal phase of the
menstrual cycle. If a 100mg/day dose has been established with luteal phase
dosing, a 50mg/day titration step for three days should be utilized at the
beginning of each luteal phase dosing period.
Zoloft should be given once a daily, either in the morning or evening.
In children and adolescents, Zoloft should be initially administered with
a 25mg/day dose in children ages 6-12, and a once daily dose of 50mg for adolescents
age 13-17. Patients not responding may benefit from dose increases up to a
maximum of 200mg/day. For children with OCD, their generally lower body weights
should be taken into consideration when increasing the dosage, in order to
avoid excess dosing. Given the 24 hour elimination half-life of sertraline,
dose changes should not occur at intervals of less than 1 week.
Zoloft Side Effects and Interactions:
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Zoloft can have a number of adverse side effects, including asthenia (a feeling
of weakness without an actual loss in strength), diarrhea, gas, headache, indigestion,
pain, rash, sore throat, tingling sensations, vomiting, problems with vision,
insomnia, gastrointestinal disturbances, confusion, dizziness, tremors, delayed
ejaculation in men (anorgasmia), and decreased sex drive. It can induce mania
or hypomania in a small percentage of individuals. It has also been known to
cause minor weight loss.
Less common or rare side effects reported include acne, breast pain or enlargement,
fainting, double vision, dry or painful eyes, lightheadedness when standing
from a sitting or supine position, difficulties breathing, allergic reaction,
altered taste sensation, back pain, changeable emotions, difficulty swallowing,
cold clammy skin, cataracts, chest pain, fever, fluid retention, flushing,
increased salivation, increased libido, inability to stay seated, hearing problems,
frequent urination, hair loss, heart attack, general malaise, hot flushes,
low blood pressure, migraine, kidney failure lack of coordination, nasal inflammation,
hemorrhoids, hiccups, glaucoma, lack of sensation, light sensitivity, increased
salivation, inflammation of the penis, depersonalization (an “unreal” feeling),
abnormal dreams/thoughts, hallucinations, paranoia, rapid mood swings, tooth-grinding,
worsening of depressive symptoms, memory loss, nosebleed, increased urination
at night, ringing in the ears, racing heartbeat, rectal hemorrhage, respiratory
infection, skin inflammation or eruptions, edema of the wrists or ankles, irregular
heartbeat, twitching, yawn, sleepwalking and vaginal hemorrhage or discharge.
Due to the fact that sertraline is tightly bound to plasma protein, the use
of Zoloft in patients taking another drug which is tightly bound to protein,
such as digitoxin or warfarin, may cause a shift in plasma concentrations potentially
resulting in an adverse effect. Conversely, adverse effects can result from
displacement of protein bound Zoloft in other tightly bound drugs.
Patients taking sertraline should not drink alcohol during treatment. Over-the-counter
(OTC) remedies should be used with caution. Though none is known to interact
with Zoloft, interactions remain a possibility.
Concomitant use of Zoloft with other drugs may produce an increase , decrease
or alteration in the effects of either drug. It is especially important to
consult your physician before combining sertraline with the following:
- Cimetidine (Tagamet)
- Diazepam (Valium)
- Digitoxin (Crystodigin)
- Flecainide (Tambocor)
- Lithium (Eskalith, Lithobid)
- MAOIs (Nardil, Parnate)
- Other serotonin-boosting drugs like Prozac or Paxil
- Other antidepressants
such as Serzone and Elavil
- Propafenone (Rythmol)
- Warfarin (Coumadin)
- Sumatriptan (Imitrex)
- Tolbutamide (Orinase)
If you are taking the oral concentrate form of Zoloft, do not take disulfiram
(Antabuse).
Information for Parents and Kids:
Zoloft’s effects during pregnancy have not been adequately studied.
For women who are pregnant or may become pregnant, the drug should only be
taken during pregnancy if a clear need is established. It is unknown whether
Zoloft is found in breast milk, and thus, caution should be exercised when
using Zoloft during breastfeeding.
Pregnant women exposed to Zoloft (and other SSRIs or SNRIs) late in the third
trimester have developed complications requiring prolonged hospitalization,
respiratory support, and tube feeding. When treating pregnant women with Zoloft
in their third trimester, the physician should carefully weigh the potential
risks and benefits of treatment. The doctor may consider tapering Zoloft dosage
in the third trimester.
In June 2003, the UK banned sertraline for use in children under 18 after
studies indicated a link to increasing suicidal rates. Similar concern has
been expressed widely in the US, where only fluoxetine (another SSRI) has been
officially banned by the FDA for treating depression in minors. However, because
the antidepressant-suicide link is correlational, researchers do not know if
the increased risk of suicide for those taking antidepressants occurs because
the drugs make people suicidal, if suicide occurs because the drugs un-depress
people enough to motivate them to actually commit suicide (a popular theory),
or because of a third, as yet unknown factor.
Safety and efficacy of sertraline has not been established for children under
6 years of age.
Warnings and Precautions:
Individuals with MDD (both adult and pediatric) may experience worsening of
their depression and/or the development of suicidal ideation and behavior or
unusual changes in behavior, whether or not they are using antidepressants.
There has long been concern that antidepressants may have a role in inducing
worsening of depression and the emergence of suicidality in certain patients.
Antidepressants increased the risk of suicidal thoughts and action in short-term
studies in children and adolescents with MDD and other psychiatric ailments.
All pediatric patients taking antidepressants for any indication should be
closely observed for clinical worsening, suicidality, and unusual changes in
behavior, especially during the initial stages of treatment, or at times of
dose changes, either increases or decreases.
Adults with MDD or co-morbid depression in the setting of other psychiatric
conditions should be observed similarly for worsening depression and suicidality,
especially during the initial stages of drug therapy, or at times of dose changes,
either increases or decreases.
Such symptoms as agitation, anxiety, panic attacks, insomnia, irritability,
hostility/aggressiveness, impulsivity, hypomania, psychomotor restlessness
and mania have been reported in adult and pediatric patients with MDD who have
been treated with antidepressants, as well as for other indications, both psychiatric
and non-psychiatric. Though no causal link has been established between the
emergence of such symptoms and either worsening depression or the emergence
of suicidal impulses, there is concern that such symptoms may be precursors
to emerging suicidality.
If a decision is made to discontinue Zoloft treatment, the medication should
be tapered, as rapidly as is feasible, but while recognizing that abrupt cessation
may produce or be linked to certain adverse reactions.
Clinical studies of the use of Zoloft in elderly patients indicate that in
persons with MDD, there doesn’t appear to be any overall difference in
the pattern of adverse reactions to those reported by younger patients. As
with all medications, greater sensitivity of some older persons cannot be ruled
out. The only standout difference was the occurrence of urinary tract infection
in a percentage of elderly subjects.
As with other SSRIs, sertraline has been associated with cases of clinically
significant hyponatremia in the elderly.
Withdrawal:
Pre-marketing clinical experience with Zoloft did not uncover any tendency
for drug-seeking behavior, dependence or withdrawal syndrome. As with any CNS
active drug, however, physicians should carefully assess patients for history
of drug abuse and observe such individuals closely for signs of misuse or abuse
(e.g., development of tolerance, drug-seeking behavior, incrementation of dose).
Over-dosage & Contraindications:
As of 1999, of 1,027 cases of overdose involving sertraline worldwide, alone
or in conjunction with other drugs, there were 72 deaths.
Among 634 cases in which sertraline was the only drug ingested, 8 overdoses
resulted in fatal outcome, 75 completely recovered, and 27 patients experienced
sequelae (a secondary consequence or condition as a result of the overdose)
after overdosage to include decreased sex drive, alopecia, difficulty ejaculating
(men), fatigue, diarrhea, insomnia, drowsiness (somnolence) and serotonin syndrome.
The remaining 524 cases had an undetermined outcome. The most common signs
and symptoms seen with non-fatal sertraline overdose were somnolence, vomiting,
tachycardia (rapid heartbeat), dizziness, agitation, tremor and nausea.
The largest known ingestion was 13.5 grams in a patient who took Zoloft alone
and subsequently recovered. However, another patient who ingested 2.5 grams
of sertraline alone experienced a fatal outcome.
Other important adverse occurrences associated with Zoloft overdose (alone
or with other drugs) include coma, convulsions, delirium, bradycardia (unusually
slow heartbeat), serotonin syndrome, stupor, manic reaction, pancreatitis,
hallucinations, hypotension (low blood pressure), hypertension (high blood
pressure) and syncope (blackout).
In managing Zoloft overdose treatment should consist of those general measures
employed in the management of overdosage of any antidepressant.
An adequate airway should be maintained, along with oxygenation and ventilation.
Monitor cardiac rhythm and vital signs. General supportive and symptomatic
measures are also recommended. Gastric lavage with a large-bore orogastric
tube with appropriate airway protection, if needed, may be indicated if performed
soon after ingestion, or in symptomatic patients.
Activated charcoal should be administered. Due to this drug’s large
volume of distribution, forced diuresis, dialysis, hemoperfusion and exchange
transfusion are unlikely to have benefit. There are no known antidotes for
sertraline.
In managing overdosage, the possibility of multiple-drug ingestion should
be kept in mind. The physician may consider contacting a poison control center
when treating an overdose.
Concomitant use in patients taking MAOIs is contraindicated. Use of Zoloft
in conjunction with pimozide is not recommended. The drug is also contraindicated
in patients exhibiting a hypersensitivity to sertraline or any of its active
ingredients.
The oral concentration of Zoloft is contraindicated with Antabuse (disulfiram)
due to the concentrate’s alcohol content.
Generic Name: sertraline
Chemical Formula: C17H17NCl2•HCl
Routes of Administration: oral
Elimination Half Life: 26 hours
Legal Status: by prescription only
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