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Celexa

Generic Celexa is a high-quality medication which is taken in treatment of depression, panic disorder, premenstrual dysphoric disorder in women, social phobia, alcoholism, eating disorders. Generic Celexa acts by balancing your brain.

Other names for this medication:
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Also known as:  Citalopram.

Description

Generic Celexa is a perfect remedy in struggle against depression. Its target is to treat panic disorder, premenstrual dysphoric disorder in women, social phobia, alcoholism, eating disorders. Generic Celexa acts by balancing your brain.

Generic name of Generic Celexa is Citalopram.

Celexa is also known as Citalopram, Cilo, Cipramil, Citrol, Seropram, Recital, Zetalo, Celepram, Ciazil, Zentius, Cipram.

Brand name of Generic Celexa is Celexa.

Dosage

Take Generic Celexa tablets and liquid form orally with or without food.

Do not crush or chew it.

Take Generic Celexa once a day at the same time.

If you want to achieve most effective results do not stop taking Generic Celexa suddenly.

Overdose

If you overdose Generic Celexa and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of reach of children.

Side effects

The most common side effects associated with Celexa are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Generic Celexa if you are allergic to Generic Celexa components.

Do not take Generic Celexa if you are pregnant, planning to become pregnant, or are breast-feeding.

Do not take it if you are under 18. For elderly patient there is a special dosage.

Be careful with Generic Celexa if you suffer from or have a history of liver or kidney disease; heart attack; seizures; bipolar disorder; epilepsy; suicidal thoughts, drug dependence.

Be careful with Generic Celexa if you take lithium (such as Eskalith, Lithobid); blood thinner (warfarin (such as Coumadin)); naratriptan (such as Amerge), almotriptan (such as Axert), zolmitriptan (such as Zomig), rizatriptan (such as Maxalt), frovatriptan (such as Frova), sumatriptan (such as Imitrex); carbamazepine (such as Tegretol); other antidepressants such as imipramine (such as Tofranil), fluoxetine (such as Sarafem, Prozac), amitriptyline (such as Elavil), escitalopram (such as Lexapro), paroxetine (such as Paxil), sertraline (such as Zoloft), fluvoxamine (such as Luvox), nortriptyline (such as Pamelor); cimetidine (such as Tagamet), MAOI (monoamine oxidase inhibitor) (phenelzine (such as Nardil), isocarboxazid (such as Marplan), selegiline (such as Emsam, Eldepryl), tranylcypromine (such as Parnate), rasagiline (such as Azilect), medicines which cause sleepiness.

Avoid alcohol.

Be careful! Taking Generic Celexa you can become suicidal.

It can be dangerous to stop Generic Celexa taking suddenly.

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To evaluate the economic impact of implementing a sertraline (Zoloft--Pfizer) tablet-splitting program on the Nebraska Medicaid program based on the change in total and per-member-per-month (PMPM) prescription drug costs and to identify any real or perceived problems with tablet splitting using switches among selective serotonin reuptake inhibitors (SSRIs) as a proxy indicator.

70 mg celexa

Background: Cataplexy is a disabling component of the narcolepsy tetrad that is sometimes resistant to standard treatment.Case reports: Three of our patients with narcolepsy, including one who had post-traumatic narcolepsy, suffered from intractable cataplexy with failure of treatment with established drugs due to unacceptable side-effects.Results: We explored the use of citalopram (Celexa), the newest and most specific of the serotonin reuptake inhibitors, and were successful in treating cataplexy without significant side-effects. Stimulant drugs remained necessary for controlling symptoms of excessive drowsiness.Conclusions: Citalopram was effective in relieving the symptoms of resistant cataplexy in out patients.

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All 14,520 patients who received an SSRI during the study period, including 5,466 patients who received at least one prescription for sertraline.

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In this article, we explore the accelerated penetration of generic antidepressants in the United States market following the availability of generic citalopram and sertraline. Analysis suggests that overall, generic penetration into the antidepressant market has grown from approximately 41 percent in January 2004 to over 73 percent in January 2010. Similar trends are uncovered when branded and generic prescriptions are analyzed by specialty.

celexa recommended dosage

None.

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Deconstruction of court documents revealed that protocol-specified outcome measures showed no statistically significant difference between citalopram and placebo. However, the published article concluded that citalopram was safe and significantly more efficacious than placebo for children and adolescents, with possible adverse effects on patient safety.

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Serum spiked with the aforementioned antidepressants, along with their corresponding isotopically labeled internal standards was subjected to protein precipitation. Samples were injected onto a TFC column for on-line solid phase extraction and a Hypersil Gold C18 column for chromatographic separation. Detection was achieved using a TSQ Vantage mass spectrometer. Assay validation followed FDA bioanalytical guidelines.

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Retrospective study of prescription claims before and after the tablet-splitting program was implemented.

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Active Pharmaceutical Ingredients (APIs) are released into aquatic ecosystems through discharged sewage wastewater. Antidepressants are among those APIs often detected in wastewater effluent and have been recently reported to cause foot detachment from the substrate in freshwater snails. We tested the effects of four commonly prescribed antidepressants {fluoxetine ("Prozac"), fluvoxamine ("Luvox"), venlafaxine ("Effexor"), and citalopram ("Celexa") on adhesion to the substrate in five species of marine snails, three from the Pacific coast (Chlorostoma funebralis, Nucella ostrina, Urosalpinx cinerea) and two species from the Atlantic coast (Tegula fasciatus and Lithopoma americanum) of North America representing three different gastropod families. All antidepressants tested induced foot detachment from the substrate in all snail species in a mainly dose-dependent manner (p < 0.04-0.00000001). The lowest LOECs (lowest observed effect concentration) for antidepressants and snails were recorded for Lithopoma in 43.4 μg/L (100 nM) fluvoxamine and Chlorostoma in 157 μg/L (500 nM) venlafaxine and 217 μg/L (500 nM) fluvoxamine. The trochids and turbinids were 2-10× more sensitive to the antidepressants than the muricids. Latency to detachment was also dose dependent, with the fastest average times to detach seen in Chlorostoma and Lithopoma (7.33 and 13.16 min respectively in 3.13 mg/L venlafaxine). The possible physiological mechanisms regulating antidepressant-induced foot detachment in marine snails and the possible ecological consequences are discussed.

celexa drug classification

In August 2011, the U.S. Food and Drug Administration issued a drug safety communication that the antidepressant drug citalopram (Celexa®) should not be used at dosages greater than 40 mg per day (or greater than 20 mg per day for patients 60 and older) because higher doses have been associated with abnormal heart rhythms. Clinical studies using citalopram in patients with cardiac disease and in older patients do not confirm such a risk. The major metabolite of citalopram is demethylcitalopram, which is subsequently metabolized to the minor metabolite didemethylcitalopram (DDCT). High DDCT concentrations have been associated with QT interval prolongation in beagle dogs. Therapeutic drug monitoring study data suggest that routine or even high oral doses of citalopram are unlikely to result in cardiotoxic concentrations of the DDCT metabolite. Based on evidence taken from a wide variety of studies, the citalopram dose limitations described in the safety announcement do not have strong clinical justification.

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Using two years (2011-2012) of usage logs from UpToDate, we measured the volume of searches related to medical conditions with significant burden in the United States, as well as the seasonal distribution of those searches. We quantified the relationship between searches and resulting page views. Using a large collection of online mainstream media articles and Web log posts we also characterized the uptake of a Food and Drug Administration (FDA) alert via changes in UpToDate search activity compared with general online media activity related to the subject of the alert.

celexa dosage information

The development and validation of this TFC-MS/MS method allow for the robust and high-throughput quantification of commonly prescribed antidepressants.

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celexa dosage 2016-03-04

Drugs take effect at different times in different individuals. Consequently, researchers seek to examine how the timing of the biological response to Glucotrol And Alcohol drugs may be affected by factors such as gender, genotypes, age, or baseline symptom scores.

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In the central nervous system (CNS) and in the periphery, specific proteins (transporters) are responsible for the regulation of the synaptic concentrations of the major monoamine neurotransmitters, noradrenaline (NE), serotonin (5-HT) and dopamine (DA). Several reports have shown that the expression of these transporters within the CNS may be altered in patients with certain neurodegenerative or neuropsychiatric disorders. Therefore, in the CNS the monoamine transporters are major targets for existing and developmental drugs. The best known drugs targeting these transporters are the selective 5-HT reuptake inhibitors (SSRIs) (e.g. citalopram, Celexa) that are Neurontin 4800 Mg most frequently used in the treatment of clinical depression. Selective NE reuptake inhibitors (NRIs) have also found use for the treatment of depression and other conditions such as attention deficit hyperactivity (ADHD) disorder. Given that the NE transporter (NET) is also a binding site for cocaine and drugs of abuse, there is a great need for a probe to assess the densities of NET in vivo by brain imaging with either positron emission tomography (PET) or single photon emission tomography (SPET). PET in particular has the potential to measure NET densities quantitatively and with high resolution in the human brain in vivo. The quality of a PET image depends crucially on the radioligand used in the emission measurement. Commonly used radionuclides in PET radioligands are carbon 11 (t(1/2) = 20.4 min) and fluorine-18 (t(1/2) = 109.8 min). This review specifically summarizes the present status of the development of (11)C- or (18)F-labeled ligands as tools for imaging NET in brain with PET in support of neuropsychiatric clinical research and drug development.

70 mg celexa 2017-07-06

Diseases and symptoms dominate UpToDate searches. Some searches result in page views of only short duration, while others consistently result in longer-than-average page views. The response to an FDA alert for Celexa, characterized by a change in UpToDate search activity, differed considerably from general online media activity Cefixime Tablets 200mg . Changes in search activity appeared later and persisted longer in UpToDate logs. The volume of searches and page view durations related to Celexa before the alert also differed from those after the alert.

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To analyze health care Imitrex 6 Mg professionals' information-seeking behavior and assess the feasibility of measuring drug-safety alert response from the usage logs of an online medical information resource.

celexa good reviews 2015-09-18

Generic agents do not require large clinical trials of safety and efficacy to enter the market, although they must demonstrate both pharmacological and bioequivalence to the brand name drug. Bioequivalence is attained when the extent of absorption of the generic falls within an FDA predefined range relative to the brand Rulide Renal Dose name drug. This potential variation in bioequivalence is not thought to be clinically meaningful, however, there are reports of a lack of therapeutic equivalence between some generic medications and the brand name. This study examines the potential risks posed by a switch from Celexa to generic citalopram. Twenty patients at an Anxiety Disorders Clinic who were unknowingly switched to generic citalopram, from Celexa (Lundbeck, Montreal, Quebec, Canada) and experienced a re-emergence of their anxiety symptoms or development of new adverse events are described in this case series report. The mean time for re-emergence of symptoms or development of adverse events was 3.4 +/- 1.6 weeks (range 0.5-8 weeks). All patients reestablished previous treatment response with a change back to Celexa in a mean time of 3.8 +/- 2.6 weeks (range 0.7-12 weeks). Given these results, it is important for clinicians to be aware of the potential for loss of treatment effect or symptom re-emergence posed by a switch to a generic agent. Randomized, double blind, controlled investigations would likely provide useful information as current bioequivalence and pharmacological equivalence do not necessarily translate into clinical equivalence.

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Thirty-three witnessed cat SSRI ingestions Actos Generic Cost .

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To evaluate the economic impact of implementing a sertraline (Zoloft--Pfizer) tablet-splitting program on the Nebraska Medicaid program based on the change in total and per-member-per-month (PMPM Risperdal Cost ) prescription drug costs and to identify any real or perceived problems with tablet splitting using switches among selective serotonin reuptake inhibitors (SSRIs) as a proxy indicator.

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Deconstruction of court documents revealed that protocol-specified Amaryl Diabetes Pill outcome measures showed no statistically significant difference between citalopram and placebo. However, the published article concluded that citalopram was safe and significantly more efficacious than placebo for children and adolescents, with possible adverse effects on patient safety.

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To evaluate a population of cats with selective-serotonin reuptake inhibitor (SSRI) toxicosis and characterize the population affected, list products ingested, the clinical signs observed, treatments performed, length of hospitalization, patient outcome, and overall prognosis.

celexa drug 2017-05-05

Serotonin (5-HT), a well-known neurotransmitter of the central nervous system, has been implicated in diverse aspects of immune regulation. Here we show that 5-HT can efficiently drive programmed cell death in established Burkitt lymphoma (BL) lines that remain faithful to the original biopsy phenotype (group 1). Group 1 BL cells cultured in the presence of 5-HT exhibited marked suppression of DNA synthesis that was accompanied by extensive apoptosis-serotonin-driven apoptosis was complete within 24 hours, was preceded by early caspase activation, and was accompanied by a decline in mitochondrial membrane potential. BL cells that had drifted to a lymphoblastic group 3 phenotype were relatively resistant to these actions of serotonin, and the forced ectopic expression of either bcl-2 or bcl-x(L) provided substantial protection from 5-HT-induced apoptosis. 5-HT receptor antagonists (SDZ205-557, granisetron, methysergide) failed to inhibit serotonin-induced apoptosis, whereas the selective serotonin reuptake inhibitors (SSRI)-fluoxetine (Prozac), paroxetine (Paxil), and citalopram (Celexa)-substantially blocked the monoamine actions. Western blot analysis showed that BL cells expressed protein for the 5-HT transporter, and transport assays confirmed active uptake of serotonin by the cells. Unlike what was suggested for neuronal cells, there was no evidence that intracellular oxidative metabolites were responsible for the 5-HT-induced programmed death of BL cells. These data indicate that serotonin drives apoptosis in biopsylike BL cells after its entry through an active transport mechanism, and they suggest a novel therapeutic modality for Burkitt lymphoma.