Citalopram Brown
Citalopram Brown Uses, Dosage, Side Effects, Food Interaction and all others data.
Citalopram Brown is an orally administered selective serotonin reuptake inhibitor (SSRI) with a chemical structure unrelated to that of other SSRIs, tricyclic, tetracyclic or other available antidepressant agents. The mechanism of action of Citalopram Brown as an antidepressant is presumed to be linked to potentiation of serotonergic activity in central nervous system resulting from its inhibition of CNS neuronal reuptake of serotonin (5-HT).
Citalopram Brown belongs to a class of antidepressants known as selective serotonin reuptake inhibitors (SSRIs). It has been found to relieve or manage symptoms of depression, anxiety, eating disorders and obsessive-compulsive disorder among other mood disorders. The antidepressant, anti-anxiety, and other actions of citalopram are linked to its inhibition of CNS central uptake of serotonin . Serotonergic abnormalities have been reported in patients with mood disorders. Behavioral and neuropsychological of effects of serotonin include the regulation of mood, perception, reward, anger, aggression, appetite, memory, sexuality, and attention, as examples. The onset of action for depression is approximately 1 to 4 weeks. The complete response may take 8-12 weeks after initiation of citalopram .
In vitro studies demonstrate that citalopram is a strong and selective inhibitor of neuronal serotonin reuptake and has weak effects on norepinephrine and dopamine central reuptake. The chronic administration of citalopram has been shown to downregulate central norepinephrine receptors, similar to other drugs effective in the treatment of major depressive disorder. Citalopram Brown does not inhibit monoamine oxidase .
| Trade Name | Citalopram Brown |
| Availability | Prescription only |
| Generic | Citalopram |
| Citalopram Other Names | Citalopram, Citalopramum, Nitalapram |
| Related Drugs | Rexulti, sertraline, trazodone, fluoxetine, Lexapro, amitriptyline, venlafaxine, Zoloft, Cymbalta, Prozac |
| Type | |
| Formula | C20H21FN2O |
| Weight | Average: 324.3919 Monoisotopic: 324.163791509 |
| Protein binding | Citalopram, dimethylcitalopram, and didemethylcitalopram are 80% bound to plasma proteins . |
| Groups | Approved |
| Therapeutic Class | SSRIs & related anti-depressant drugs |
| Manufacturer | |
| Available Country | Portugal |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
Citalopram Brown is used for depressive illness and panic disorder. It is also used for substance abuse disorders and alcohol dependence. Citalopram Brown has also been given in variety of anxiety disorders including obsessive-compulsive disorder and social phobia. It is also effective in generalized anxiety disorder, post-traumatic stress disorder, premenstrual syndrome, idiopathic Parkinson's disease and eating disorder.
Citalopram Brown is also used to associated treatment for these conditions: Anorexia Nervosa (AN), Bulimia Nervosa, Depression, Diabetic Neuropathies, Major Depressive Disorder (MDD), Obsessive Compulsive Disorder (OCD), Panic Disorder, Post Traumatic Stress Disorder (PTSD), Premature Ejaculation, Premenstrual Dysphoric Disorder, Social Anxiety Disorder (SAD)
How Citalopram Brown works
The mechanism of action of citalopram results from its inhibition of CNS neuronal reuptake of serotonin (5-HT) . The molecular target for citalopram is the serotonin transporter (solute carrier family 6 member 4, SLC6A4), inhibiting its serotonin reuptake in the synaptic cleft .
Citalopram Brown binds with significantly less affinity to histamine, acetylcholine, and norepinephrine receptors than tricyclic antidepressant drugs . This drug has no or neglible affinity for 5-HT1A, 5-HT2A, dopamine D1 and D2, α1-, α2-, and_ β adrenergic, _histamine H1, gamma-aminobutyric acid (GABA), muscarinic, cholinergic, and benzodiazepine receptors. Antagonism of muscarinic, histaminergic, and adrenergic receptors is thought to be associated with several anticholinergic, sedative, and cardiovascular effects of other psychotropic drugs .
Dosage
Citalopram Brown dosage
Depressive illness 20 mg daily as a single dose in the morning or evening; increased ifnecessary to maximum 60 mg daily (Elderly maximum 40 mgdaily).Panic disorder Initially 10 mg daily, increased to 20 mg after 7 days; usual dose 20-30 mg daily; maximum 60 mg daily (Elderly maximum 40 mgdaily).
Side Effects
SSRIs are less sedating and have fewer antimuscarinic and cardiotoxic effects than tricyclic antidepressants. However, side-effects may be seen, includes gastro-intestinal effects (nausea, vomiting, dyspepsia, abdominal pain, diarrhoea, constipation), anorexia with weight loss, palpitations, tachycardia, postural hypotension, cough, confusion, impaired concentration, amnesia, urinary retention, sweating, movement disorders, urticaria, anaphylaxis, arthralgia, myalgia and photosensitivity.
Toxicity
Oral (Human) LD: 56 mg/kg Intraperitoneal (Mouse) LD50: 179 mg/kg
Acute toxicity
Symptoms of toxicity include dizziness, sweating, nausea, vomiting, tremor, somnolence, and sinus tachycardia. Rarely, symptoms included amnesia, confusion, coma, convulsions, hyperventilation, cyanosis, rhabdomyolysis, and ECG changes (including QTc prolongation, nodal rhythm, ventricular arrhythmia, and extremely rare cases of cardiac torsade de pointes) may occur. Acute renal failure has been a rare occurrence .
In cases of overdose, establish and maintain the airway to ensure adequate ventilation and oxygen delivery. Due to the large volume of distribution of citalopram, forced diuresis, dialysis, hemoperfusion, and exchange transfusion are unlikely to be of benefit. Gastric evacuation by lavage and use of activated charcoal should be considered. Careful observation and cardiac and vital sign monitoring are advised, in addition to supportive care. With the large volume of distribution of citalopram, forced diuresis, dialysis, hemoperfusion, and exchange transfusion are unlikely to be of benefit .
Pregnancy
This drug is categorized as pregnancy category C. In animal reproduction studies, citalopram has been shown to have adverse effects on embryo/fetal and postnatal development, which includes teratogenic effects when given at doses higher than human therapeutic doses. There are no sufficient and well-controlled studies in pregnant women; therefore, citalopram should be used during pregnancy only in cases where the potential benefit justifies the possible risk to the fetus .
Pregnancy-Nonteratogenic Effects
Neonates exposed to celexa and other SSRIs or SNRIs, late in the third trimester, have undergone complications requiring prolonged hospitalization, respiratory support, and parenteral feeding. Complications such as these can arise immediately upon delivery .
Nursing Mothers
Citalopram Brown is excreted in human breast milk. There have been two reports of infants demonstrating high levels of somnolence, reduced feeding, and weight loss associated with breastfeeding from a mother taking citalopram. In one specific case, the infant was reported to recover completely after the discontinuation of citalopram. In the second case, no follow-up information was available for assessment. The decision whether to continue or discontinue either nursing or celexa should consider the risks of citalopram exposure for the infant versus the benefits of celexa treatment for the mother .
Precaution
Caution should be taken in patients with epilepsy, concurrent electroconvulsive therapy, history of mania, cardiac disease, diabetes mellitus, angle-closure glaucoma, history of bleeding disorders, hepatic and renal impairment. Abrupt withdrawal of Citalopram Brown should be avoided.
Interaction
Ketoconazole, Itraconazole or Macrolide antibiotics and Citalopram Brown co-administration decreases the metabolism of Citalopram Brown. Omeprazole and Citalopram Brown co-administration might decrease the clearance of Citalopram Brown.
Food Interaction
- Avoid alcohol.
- Avoid St. John's Wort.
- Take with or without food. The absorption is unaffected by food.
[Moderate] GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of CNS-active agents.
Use in combination may result in additive central nervous system depression and
MANAGEMENT: Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol.
Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
Citalopram Brown Drug Interaction
Moderate: aspirin, aspirin, pregabalin, pregabalin, metoprolol, metoprolol, metoprolol, metoprolol, alprazolam, alprazolamUnknown: omega-3 polyunsaturated fatty acids, omega-3 polyunsaturated fatty acids, levothyroxine, levothyroxine, cyanocobalamin, cyanocobalamin, ascorbic acid, ascorbic acid, cholecalciferol, cholecalciferol
Citalopram Brown Disease Interaction
Major: depressionModerate: renal dysfunction, hyponatremia, liver disease, mania, platelet function, QT prolongation, seizure disorders, SIADHMinor: weight loss
Volume of Distribution
12 L/kg
Citalopram Brown is highly lipophilic and likely widely distributed throughout the body, including the blood-brain-barrier. However, its metabolite, demethylcitalopram does not penetrate the blood-brain-barrier well .
Elimination Route
Rapidly and well absorbed from the GI tract. Peak plasma concentrations occur within 4 hours of a single orally administered dose. Bioavailability is 80% following oral administration. Food does not affect absorption .
Half Life
About 35 hours .
Clearance
The systemic clearance of citalopram is 330 mL/min, with approximately 20% renal clearance .
Elimination Route
12-23% of an oral dose of citalopram is found unchanged in the urine, while 10% of the dose is found in the faeces .
Pregnancy & Breastfeeding use
PregnancyThere are no adequate and well-controlled studies in pregnant women; therefore, Citalopram Brown should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
LactationCitalopram Brown is excreted in human breast milk. So, the decision whether to continue or discontinue either nursing or Citalopram Brown therapy should take into account the risks of Citalopram Brown exposure for the infants and the benefits of Citalopram Brown treatment for the mother.
Contraindication
Citalopram Brown should not be used if the patient enters a manic phase. Concomitant use in patients taking MAO inhibitor is contraindicated. Citalopram Brown is contraindicated in patients with a hypersensitivity to this drug or any of its ingredients.
Acute Overdose
It is a very safe drug. There were no reports of fatal Citalopram Brown overdose in clinical trials involving overdoses of up to 2000 mg.
Symptoms: Dizziness, sweating, nausea, vomiting, tremor, somnolence and sinus tachycardia. Rarely, amnesia, confusion, coma, seizures, hyperventilation, cyanosis, rhabdomyolysis and ECG changes (e.g. QT prolongation, sinus bradycardia, ventricular arrhythmias, nodal rhythm, torsade de pointes and left bundle branch block).
Management: Symptomatic and supportive treatment. Maintain and ensure adequate ventilation and oxygenation. Gastric evacuation by lavage and use of activated charcoal should be considered. Frequently monitor cardiac function and vital signs.
Interaction with other Medicine
Ketoconazole, Itraconazole or Macrolide antibiotics and Citalopram Brown co-administration decreases the metabolism of Citalopram Brown. Omeprazole and Citalopram Brown co-administration might decrease the clearance of Citalopram Brown.
Storage Condition
Store at 25° C.
Innovators Monograph
You find simplified version here Citalopram Brown
Citalopram Brown contains Citalopram see full prescribing information from innovator Citalopram Brown Monograph, Citalopram Brown MSDS, Citalopram Brown FDA label
FAQ
What is Citalopram Brown used for?
It is used to treat major depressive disorder, obsessive compulsive disorder, panic disorder, and social phobia. Citalopram Brown helps many people recover from depression, and has fewer unwanted side effects than older antidepressants.
How safe is Citalopram Brown?
Citalopram Brown is safe to take for a long time. A few people may get sexual side effects, such as problems getting an erection or a lower sex drive. In some cases these can continue even after stopping the medicine. Speak to your doctor if you are worried.
How does Citalopram Brown work?
Citalopram Brown work by increasing the amount of serotonin, a natural substance in the brain that helps maintain mental balance.
What are the common side effects of Citalopram Brown?
Common side effects of Citalopram Brown are include;
- nausea
- diarrhea
- constipation
- vomiting
- stomach pain
- heartburn
- decreased appetite
- weight loss
- frequent urination
- excessive tiredness
- yawning
- weakness
- uncontrollable shaking of a part of the body
- muscle or joint pain
- dry mouth
- changes in sex drive or ability
- heavy menstrual periods
Is Citalopram Brown safe during pregnancy?
Generally, these Citalopram Brown are an option during pregnancy: Certain selective serotonin reuptake inhibitors (SSRIs). SSRIs are generally considered an option during pregnancy, including Citalopram Brown and sertraline. Potential complications include maternal weight changes and premature birth.
Is Citalopram Brown safe during breastfeeding?
Several studies have shown that small amounts of Citalopram Brown are found in breast milk. There have been a few cases of sleepiness and weight loss, but in most studies no harmful effects were seen in breastfed babies.
Can I drink alcohol with Citalopram Brown?
You can drink alcohol while taking Citalopram Brown, but it may make you feel sleepy. It might be best to stop drinking alcohol until you see how the medicine makes you feel.
Can I drive after taking Citalopram Brown?
Do not drive or operate machinery until the full effects of Citalopram Brown are known as it may impair your judgment and affect your ability to drive or operate machinery.
How quickly does Citalopram Brown enter my system?
It usually takes 4 to 6 weeks for citalopram to work. Side effects such as tiredness, dry mouth and sweating are common.
When should be taken of Citalopram Brown?
You can take it with or without food. You can take Citalopram Brown at any time of day, as long as you stick to the same time every day. If you have trouble sleeping, it's best to take it in the morning.
How often can I take Citalopram Brown?
Take Citalopram Brown once a day.
How long does Citalopram Brown take to work?
It usually takes 4 to 6 weeks for Citalopram Brown to work.
How long can I take Citalopram Brown ?
Most people take Citalopram Brown for 6 months. But in some instances, a doctor may prescribe this substance for 9 months. Long-term use of antidepressants may put people at risk for type 2 diabetes, and SSRIs may cause heart rhythm abnormalities at higher doses.
Who should not take Citalopram Brown?
You should not use Citalopram Brown if you also take pimozide, as the combination can cause problems with your heart rhythm. Citalopram Brown can cause a serious heart problem. Call your doctor right away if you have chest pain, fast or pounding heartbeats, shortness of breath, and sudden dizziness. Do not use Citalopram Brown if you have used a MAO inhibitor in the past 14 days (such as isocarboxazid, linezolid, phenelzine, rasagiline, selegiline, or tranylcypromine) or have received a methylene blue injection. A fatal reaction may occur.
What happens if I miss a dose?
Take the medicine as soon as you can, but skip the missed dose if it is almost time for your next dose. Do not take two doses at one time.
What will happen If I stop taking Citalopram Brown ?
Stopping Citalopram Brown abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).
What happens if I overdose?
Citalopram Brown overdoses often have only mild to moderate symptoms, particularly with ingestions under 600 mg in adults. However, with higher doses, severe manifestations have been described, including QTc prolongation, TdP, and seizures.
Will Citalopram Brown affect my fertility?
For women, there's no firm evidence to suggest that taking Citalopram Brown will reduce your fertility. But speak to a pharmacist or your doctor if you're trying to get pregnant.
Can Citalopram Brown affects my heart ?
Taking Citalopram Brown may put you at higher risk of a serious heart rhythm change called QT prolongation, which can cause sudden death. People with slow heart rate, recent heart attack, or severe heart failure should also not take Citalopram Brown.
Can Citalopram Brown affect my kidneys?
Citalopram Brown may build up and cause more side effects in people with severe kidney disease.
