The Checkup by Singlecare

JANUARY 30, 2024

Hailing from the selective serotonin-reuptake inhibitor ( SSRI ) class of drugs, citalopram is often used for the treatment of major depressive disorder or off-label use treating anxiety disorder. For all the good work that it does, citalopram also has its downsides. These communication efforts can make all the difference.

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The Checkup by Singlecare

SEPTEMBER 8, 2023

Lexapro is a brand-name drug approved by the Food and Drug Administration (FDA) to treat major depressive disorder and generalized anxiety disorder. Healthcare providers may also prescribe it off-label for other mental health conditions, including social anxiety disorder and obsessive-compulsive disorder.

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The Checkup by Singlecare

DECEMBER 6, 2023

Food and Drug Administration (FDA) to treat epilepsy and prevent various types of seizures. SingleCare (2021) Topiramate , Epilepsy Foundation (2023) Topiramate (Oral Route) , Mayo Clinic (2023) The post Topiramate interactions to avoid appeared first on The Checkup.

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The Checkup by Singlecare

APRIL 15, 2024

Anxiety Unlike depression, anxiety is an off-label use for trazodone. Insomnia Trazodone for insomnia is another off-label use, but a fairly common one. Food and Drug Administration ( FDA ) has issued a black box warning that trazodone may also cause suicidal thoughts, primarily in young adults and children.

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The Checkup by Singlecare

APRIL 14, 2024

Food and Drug Administration (FDA), Dr. Dasgupta adds, and one of the effects of melatonin is its likelihood of causing drowsiness. When it comes to ibuprofen drug interactions , the list from the Mayo Clinic is quite lengthy. These are only a couple of examples. As a supplement, melatonin isn’t approved by the U.S.

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The Checkup by Singlecare

OCTOBER 25, 2023

UCLA Health (2018) Mobic label , U.S. Some of the most commonly reported side effects of meloxicam are: Diarrhea or constipation Upper respiratory tract infections Heartburn Flu-like symptoms Drowsiness According to the U.S.

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The Checkup by Singlecare

FEBRUARY 6, 2024

Food and Drug Administration (FDA). This drug stands out as one of the few non-stimulant options for the treatment of adults and children with attention-deficit hyperactivity disorder ( ADHD ) that are approved by the U.S.

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The Checkup by Singlecare

SEPTEMBER 25, 2023

Follow the proper label instructions for each. Canadian Family Physician (2012) Maxigesic Rapid® tablets gain US FDA approval. Mayo Clinic (2023) Pain and Fever Relief. Sources: Combined acetaminophen and ibuprofen for pain relief after oral surgery in adults: a randomized controlled trial.

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The Checkup by Singlecare

SEPTEMBER 7, 2023

First approved by the Food and Drug Administration (FDA) over 50 years ago under the brand name Inderal, it has accumulated a diverse list of uses. Nurtec has FDA indications for acute migraine relief and preventing this headache variety.

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BuzzRx

JANUARY 29, 2023

Keeping Sudafed products behind the counter, along with other regulations, was mandated by the FDA in 2006 because pseudoephedrine, the main ingredient in Sudafed products, can be used illegally to make methamphetamine. Sudafed Dose Follow the directions on the product label or your doctor’s instructions carefully.

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pharmaphorum

DECEMBER 14, 2022

The company now intends to discuss the data with regulators, with a view to expanding Blincyto’s label. “Patients who are MRD negative have a better prognosis than patients who are MRD positive, generally, but they still relapse,” commented Mark Litzow of the Mayo Clinic, who presented the data at ASH.

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The Checkup by Singlecare

FEBRUARY 13, 2023

According to the FDA , eating a balanced diet high in magnesium may reduce your risk of hypertension, but the evidence supporting that claim is still inconclusive. Read the labels. Because the FDA doesn’t regulate supplements for effectiveness or safety, some third-party organizations have taken on that job.

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The Checkup by Singlecare

DECEMBER 6, 2023

The FDA has not approved Tamsulosin for use in women and children, though at times, medical professionals may use the drug off-label in these populations for other indications. This type of adverse event should be reported to the FDA at 1-800-FDA-1088. If you miss a dose of tamsulosin, take it as soon as you remember.

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The Checkup by Singlecare

OCTOBER 3, 2023

Your interest and inquisitions will be welcomed, and as a result, you will be safer.

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The Checkup by Singlecare

DECEMBER 29, 2023

Safety measures while using CoQ10 What are the FDA warnings about CoQ10? The Food and Drug Administration (FDA) has not issued any warnings about CoQ10. It is available over the counter, so the FDA has determined that it’s safe to use without medical supervision. Who should never take CoQ10? Who should use caution with CoQ10?

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The Checkup by Singlecare

NOVEMBER 30, 2023

It is also used off-label for insulin resistance in polycystic ovary syndrome ( PCOS ). Metformin is the first-line drug of choice prescribed by medical professionals for Type 2 diabetes treatment. These agents reduce serum bicarbonate levels in the bloodstream.

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The Checkup by Singlecare

JANUARY 18, 2024

Follow the instructions on your prescription label. It’s essential that your healthcare provider know everything that you are taking before they prescribe Bactrim, as it can have interactions. Start by reading the package insert, and ask your pharmacist questions if there’s anything you don’t understand. Stay hydrated.

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The Checkup by Singlecare

DECEMBER 26, 2023

Food and Drug Administration (FDA) does not regulate nutritional supplements in the same manner in which it regulates medications. In fact, the FDA does not review dietary supplements before they’re sold to customers. And if you are already taking it, you should definitely let them know you are taking it,” Dr. Cooperman says.

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The Checkup by Singlecare

JULY 24, 2023

In addition to addressing insomnia, a melatonin supplement can be taken to treat symptoms of jet lag, sleep disorders in children, and circadian rhythm sleep disorders in the blind, according to the Mayo Clinic. Food and Drug Administration (FDA), like prescription and OTC drugs are.

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The Checkup by Singlecare

JANUARY 9, 2024

While quite effective, methotrexate therapy must be closely monitored due to toxicities, according to the Food and Drug Administration (FDA). Trexall Trexall (methotrexate) is both a chemotherapeutic used in cancer treatment and a disease-modifying immunosuppressant agent used in treating autoimmune conditions like rheumatoid arthritis.

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The Checkup by Singlecare

OCTOBER 10, 2023

Cephalexin and alcohol Product labeling does not advise alcohol avoidance with cephalexin. References: Cephalexin FDA label NIH DailyMed database Mayo Clinic drug information The post Cephalexin interactions to avoid appeared first on The Checkup.

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The Checkup by Singlecare

FEBRUARY 1, 2023

Per the Mayo Clinic, berberine may cause some side effects, including diarrhea, constipation, gas, nausea, or vomiting. Always read the label. Since the FDA does not always regulate supplements, look for a seal of quality assurance from independent organizations such as ConsumerLab.com, NSF International, and U.S.

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The Checkup by Singlecare

JANUARY 15, 2024

Food and Drug Administration (FDA) as a treatment for narcolepsy. When using Adderall off-label for depression, there are many things prescribers consider. SSRIs are the most commonly prescribed type of antidepressant —and they are approved by the FDA for this purpose. It’s also approved by the U.S.

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The People's Pharmacy

MARCH 20, 2023

At the top of the list will be “side effects” and links to places like MedlinePlus, Mayo Clinic, WebMD, Cleveland Clinic or RxList. The Origins of Most Drug Information: The source of virtually all drug information originates with the clinical trials conducted for FDA drug approval. Prozac and Sexual Side Effects!

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The Checkup by Singlecare

DECEMBER 26, 2023

Some healthcare providers may prescribe it off-label for erectile dysfunction or to women for certain conditions. Safety measures while using testosterone What are the FDA warnings about testosterone? The Food and Drug Administration (FDA) has multiple boxed warnings for testosterone therapy. Who should never take testosterone?

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The Checkup by Singlecare

OCTOBER 30, 2023

Sertraline carries multiple Food and Drug Administration (FDA) approvals, including major depressive disorder (MDD), obsessive-compulsive disorder (OCD), panic disorder, posttraumatic stress disorder (PTSD), premenstrual dysphoric disorder (PMDD), and social anxiety disorder.

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Pharmaceutical Technology

MAY 3, 2023

The US Food and Drug Administration (FDA) has granted Tenaya Therapeutics’ gene therapy TN-201 a fast track designation for the treatment of myosin binding protein C3 (MYBPC3)-associated hypertrophic cardiomyopathy (HCM). In January 2023, Tenaya announced FDA clearance for its Investigational New Drug (IND) application for TN-201.

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