The Checkup by Singlecare

JULY 30, 2024

Pet parents must immediately transport a dog to an emergency veterinary hospital if seizure activity doesn’t let up. The general rule is to bring the dog to a veterinary hospital if it has three seizures within 24 hours to catch SE early. Pet owners must start treatment at home if they can’t get to the veterinary hospital fast enough.

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The Checkup by Singlecare

FEBRUARY 8, 2024

Food and Drug Administration (FDA) has not approved tramadol for veterinary medicine. These serious adverse effects include: Extreme sedation Agitation Seizures Loss of coordination (ataxia) Call a veterinarian or go to an emergency animal hospital if serious side effects are noticed.

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The Checkup by Singlecare

AUGUST 5, 2023

Initially approved by the FDA in 1996 for ADHD, Adderall has since become a widely prescribed medication in the United States. Generic Adderall is a stimulant medication that is FDA-approved for the same conditions as its brand-name counterpart for children and adults. The Adderall shortage may be due to increased demand for the drug.

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The Checkup by Singlecare

NOVEMBER 30, 2023

Medical services covered New York Medicaid covers medically necessary services, including doctor’s visits, specialist visits, family planning services, hospital services, transportation to medical appointments, X-rays, and diagnostics. It will provide a list of options for new doctors or hospitals if you don’t already have one.

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The Checkup by Singlecare

JANUARY 9, 2025

Many people mistake it for a controlled substance. However, medical experts say this is untrue, as the prescription medication is not classified as a controlled substance by the United States Drug Enforcement Administration (DEA). Is cyclobenzaprine a controlled substance? What is cyclobenzaprine?

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The FDA Law Blog

MAY 16, 2024

Houck — Employee diversion of controlled substances from hospitals has been an issue since at least 1986 when I became a diversion investigator with the Drug Enforcement Administration (“DEA”). DEA alleged that UMHS failed to maintain complete and accurate records and failed to timely notify DEA of controlled substance thefts.

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The FDA Law Blog

FEBRUARY 11, 2025

Houck One of the most significant issues facing hospitals and other facilities is the diversion of controlled substances meant for patients by physicians, pharmacists, nurses and other trusted healthcare employees. Click here to learn more about the Opioid & Abuse Management Congress.

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The FDA Law Blog

SEPTEMBER 12, 2023

More than 40 registrants — primarily hospitals and pharmacies — have paid significant civil penalties of up to $5,000,000 to settle allegations they failed to report controlled substance thefts or significant losses to the Drug Enforcement Administration (DEA). The risks to hospitals and pharmacies are multi-faceted and growing.

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The FDA Law Blog

SEPTEMBER 26, 2023

More than 40 registrants — primarily hospitals and pharmacies — have paid significant civil penalties of up to $5,000,000 to settle allegations they failed to report controlled substance thefts or significant losses to the Drug Enforcement Administration (DEA). The risks to hospitals and pharmacies are multi-faceted and growing.

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The FDA Law Blog

JANUARY 18, 2024

Houck — In August 2023 the Food and Drug Administration (“FDA”) and Health and Human Services (“HHS”) recommended that the Drug Enforcement Administration (“DEA”) reschedule marijuana from schedule I under the federal Controlled Substances Act (“CSA”) to schedule III. By Larry K. 53,688 (Aug. 53,767 (Aug. 21 U.S.C. §

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The FDA Law Blog

JUNE 10, 2024

Houck — It seems as though we cannot get through a week without hearing about controlled substance diversion by employees at another hospital or healthcare facility. DEA, Palomar Hospital Pays $250,000 for Diverting Fentanyl ( June 3, 2024 ). By Larry K.

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The Checkup by Singlecare

JANUARY 2, 2025

Gabapentin, sold under the brand names Neurontin and Gralise, is an anticonvulsant medication thats FDA approved to treat seizures and postherpetic neuralgia, which is nerve pain after a bout of shingles. Gabapentin is also frequently used off-label to treat conditions like migraines, fibromyalgia, substance dependence, and mood disorders.

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The FDA Law Blog

APRIL 8, 2024

Department of Health and Human Services (HHS) recently published a White Paper on Policy Considerations to Prevent Drug Shortages and Mitigate Supply Chain Vulnerabilities in the United States —with input from several HHS stakeholders, including FDA, CMS, and the Administration for Strategic Preparedness and Response.

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The FDA Law Blog

NOVEMBER 29, 2022

The recommendations do not apply to inpatient hospital care, in the emergency department or other observed settings. Clinicians should review FDA-approved labeling and weigh benefits and risks before beginning pharmacologic therapy. They do apply, however, to prescribing for pain management upon discharge.

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The Checkup by Singlecare

MARCH 8, 2024

Food and Drug Administration (FDA) to manage generalized anxiety disorder. Still, it is a controlled substance and comes with the risk of drug abuse and physical dependence. It is also used off-label for other forms of anxiety, like agoraphobia, panic disorders, and acute vertigo episodes.

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The Checkup by Singlecare

JULY 30, 2023

Xanax was initially approved by the United States Food and Drug Administration (FDA) in 1981 and is still popular today. New brand-name drugs go through extensive testing in order to be approved by the FDA. Clinical studies Generic and brand-name drugs contain the same active ingredients and have the same FDA-approved uses.

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OctariusRx

JUNE 5, 2023

Is the pharmacy providing the compounded drugs an FDA registered 503B outsourcing facility ? Department of Health and Human Services Office of Inspector General , about 11% of hospitals get compounded drugs from sources that are not registered with the FDA. According to a 2019 report from the U.S.

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OctariusRx

JUNE 7, 2022

Is the pharmacy providing the compounded drugs an FDA registered 503B outsourcing facility ? Department of Health and Human Services Office of Inspector General , about 11% of hospitals get compounded drugs from sources that are not registered with the FDA. According to a 2019 report from the U.S.

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The Checkup by Singlecare

JULY 17, 2023

Compare phenobarbital alternatives | Dilantin | Lamictal | Neurontin | Tegretol | Topamax | Natural alternatives | How to switch meds Phenobarbital is an FDA-approved prescription medication used to treat seizure disorders. Food and Drug Administration (FDA). Phenobarbital is a controlled substance and can be habit-forming.

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The FDA Law Blog

MAY 21, 2024

Houck — Last August Health and Human Services (“HHS”) recommended rescheduling marijuana from schedule I under the federal Controlled Substances Act (“CSA”) to schedule III. Schedules of Controlled Substances: Rescheduling of Marijuana, 89 Fed. By Larry K. 44,597 (May 21, 2024). 29, 2023) (“Basis”); NPRM at 44,603.

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The FDA Law Blog

DECEMBER 14, 2023

They contended that access to cannabis is associated with reduced rates of: Opioid use and abuse; Opioid-related hospitalizations; Opioid-related traffic fatalities; Opioid-related drug treatment admissions; and Opioid-related overdose deaths. Riley Griffin et al., US Health Officials Urge Moving Pot to Lower-Risk Tier, Bloomberg News (Aug.

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