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Fluvoxamine


Luvox (Fluvoxamine Maleate Tablets) Side Effects, Interactions

8.18.2017 | Victoria Miers

Fluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI) belonging to the chemical series, the 2-aminoethyl oxime ethers.

The reactions in OCD studies with a two-fold increase in rate compared to reaction rates in OCD and depression studies were: asthenia, abnormal ejaculation (mostly delayed ejaculation), anxiety, rhinitis, anorgasmia (in males), depression, libido decreased, pharyngitis, agitation, impotence, myoclonus/twitch, thirst, weight loss, leg cramps, myalgia, and urinary retention. These reactions are listed in order of decreasing rates in the OCD trials.

At least 14 days should elapse between discontinuation of an MAOI intended to treat psychiatric disorders and initiation of therapy with Fluvoxamine Maleate Tablets.

Fluvoxamine Oral Uses, Side Effects, Interactions, Pictures

9.19.2017 | Abigail Hoggarth

Find patient medical information for Fluvoxamine Oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings.

Low levels of potassium or magnesium in the blood may also increase your risk of QT prolongation. This risk may increase if you use certain drugs (such as diuretics " water pills ") or if you have conditions such as severe sweating, diarrhea, or vomiting. Talk to your doctor about using fluvoxamine safely.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

The risk of serotonin syndrome /toxicity increases if you are also taking other drugs that increase serotonin.

Fluvoxamine Indications, Side Effects, Warnings

11.21.2017 | Victoria Miers

Easy to read patient leaflet for fluvoxamine. Includes indications, proper use, special instructions, precautions, and possible side effects.

Families and caregivers must closely watch patients who take fluvoxamine. l the doctor right away if the patient has symptoms like worsened depression, suicidal thoughts, or changes in behavior. It is important to keep in close contact with the patient's doctor. Discuss any questions with the patient's doctor.

Approval History Calendar Drug history at FDA.

Pregnancy Category C Risk cannot be ruled out.

If fluvoxamine is prescribed for your child, talk with the doctor to be sure that fluvoxamine is right for your child.

Fluvoxamine MedlinePlus Drug Information

7.17.2017 | Logan Kirk

Fluvoxamine: learn about side effects, dosage, special precautions, and more on MedlinePlus.

Call your doctor if you have any unusual problems while you are taking this medication. Fluvoxamine may cause other side effects.

Children, teenagers, and young adults who take antidepressants to treat depression or other mental illnesses may be more likely to become suicidal than children, teenagers, and young adults who do not take antidepressants to treat these conditions. However, experts are not sure about how great this risk is and how much it should be considered in deciding whether a child or teenager should take an antidepressant.

Fluvoxamine

10.20.2017 | Abigail Hoggarth

Fluvoxamine is a medication which functions as a selective serotonin reuptake inhibitor (SSRI) and σ1 receptor agonist. Fluvoxamine is used primarily for the.

Some evidence shows fluvoxamine may be a helpful adjunct in the treatment of schizophrenia, improving the depressive, negative, and cognitive symptoms of the disorder. Its actions at the sigma receptor may afford it a unique advantage among antidepressants in treating the cognitive symptoms of schizophrenia.

By so doing, fluvoxamine can increase serum concentration of the substrates of these enzymes.

The FDA has added a black box warning for this drug in reference to increased risks of suicidal thoughts and behavior in young adults and children.

Fluvoxamine has been observed to increase serum concentrations of mirtazapine, which is mainly metabolized by CYP1A2, CYP2D6, and CYP3A4, by 3- to 4-fold in humans.