The following table lists the medications commonly used in the management of MS. For each product, the table gives the generic or chemical name, the brand name, and the common usage in MS, as well as its availability in the United States and Canada. Products available without a prescription are so indicated.

 


GENERIC NAME

BRAND NAME2

USAGE IN MS

Alprostadil

Prostin VR

Erectile dysfunction

Alprostadil

MUSE

Erectile dysfunction

Amantadine

 

Fatigue

Amitriptyline

Elavil

Pain (paresthesias)

Baclofen

Lioresal

Spasticity

Bisacodyl1

Dulcolax

Constipation

Bupropion

Wellbutrin

Depression

Carbamazepine

Tegretol

Pain (trigeminal neuralgia)

Ciprofloxacin

Cipro

Urinary tract infections

Clonazepam

Klonopin (US);

 Rivotril (Can)

Tremor; Pain; Spasticity

Dantrolene

Dantrium

Spasticity

Desmopressin

DDAVP Nasal Spray

Urinary frequency

Dexamethasone

Decadron

Acute exacerbations

Diazepam

Valium

Spasticity (muscle spasms)

Docusate1

Colace

Constipation

Docusate mini enema1

Therevac Plus (US)

Constipation

Fluoxetine

Prozac

Depression; Fatigue

Gabapentin

Neurontin

Pain (dysesthesias; spasticity)

Glatiramer acetate

Copaxone

Disease modifying agent

Glycerin1

Sani-Supp supository (US)

Constipation

Hydroxyzine

Atarax

Paroxysmal itching

Imipramine

Tofranil

Bladder dysfunction; Pain

Isoniazid

Laniazid

Tremor

Interferon beta-1a

Avonex

Disease modifying agent

Interferon beta-1a

Rebif (Canada)

Disease modifying agent

Interferon beta-1b

Betaseron

Disease modifying agent

Magnesium hydroxide1

Phillips’ Milk of Magnesia

Constipation

Meclizine

Antivert (US);

Bonamine (Can)

Nausea; Vomiting; Dizziness

Methenamine

Hiprex, Mandelamine (US);

Hip-rex, Mandelamine (Can)

Urinary tract infections (preventative)

Methylprednisolone

Depo-Medrol

Acute exacerbations

Mineral oil1

 

Constipation

Mitoxantrone

Novantrone

Disease modifying agent

Nitrofurantoin

Macrodantin

Urinary tract infections

Nortriptyline

Pamelor (US);

Aventyl (Can)

Pain (parasthesias)

Oxybutynin

Ditropan

Bladder dysfunction

Oxybutynin

(extended release formula)

Ditropan XL

Bladder dysfunction

Papaverine

 

Erectile dysfunction

Paroxetine

Paxil

Depression

Pemoline

Cylert

Fatigue

Phenazopyridine

Pyridium

Urinary tract infections (symptom relief)

Phenytoin

Dilantin

Pain (dyesthesias)

Prednisone

Deltasone

Acute exacerbations

Propantheline bromide

Pro-Banthine

Bladder dysfunction

Psyllium hydrophilic mucilloid1

Metamucil

Constipation

Sertraline

Zoloft

Depression

Sildenafil

Viagra

Erectile dysfunction

Sodium phosphate1

Fleet Enema

Constipation

Sulfamethoxazole

Bactrim; Septra

Urinary tract infections

Tizanidine

Zanaflex

Spasticity

Tolterodine

Detrol (US)

Bladder dysfunction

Venlafaxine

Effexor

Depression


1
Available without a prescription.

2Available in both US and Canada unless otherwise noted.

list provided by the NMSS

 

Diabetes Drugs May Help Multiple Sclerosis Sufferers

Source: AScribe Newswire
by: University of Illinois at Chicago

06/12/2002





CHICAGO -- Drugs currently used to treat Type 2 diabetes may
also prove useful for treatment of multiple sclerosis, according to studies at the University of

Illinois at Chicago and the West Side Veterans Administration Hospital.

The results are published in the June issue of the journal Annals of Neurology.

Douglas Feinstein, a research associate professor of anesthesiology at UIC, says two antidiabetic drugs called thiazolidinediones, or TZDs, already approved by the Food and Drug Administration for treatment of Type 2 diabetes, prevented the development of an animal model of MS in the studies.

Other tests, already under way, are designed to test if the drugs could also be effective in other neurological diseases, including Alzheimer's, Parkinson's and
stroke, he says.

The drugs prevented the MS-like disease known as experimental autoimmune encephalomyelitis from occurring in healthy mice and reduced symptoms when
given to mice that were already ill. Moreover, the drugs were effective in two different models of the disease, a chronic form in which the mice became ill and remained sick and a model in which the mice developed a relapsing form of the disease, which is similar to the more prevalent form of MS.

The antidiabetic TZDs used in the study were originally developed to increase the body's sensitivity to the low levels of insulin present in Type 2 diabetes. Rather than influencing the amount of insulin in the body, these insulin sensitizing drugs increase the ability of cells and tissue to take up the correct amount of glucose, Feinstein explains.

However, more recent studies demonstrate that the drugs carry out other actions, he says. The drugs prevent the activation and growth of lymphocytes and reduce the production of inflammatory substances by activated brain cells. He and his colleagues believe this may be the primary way the drugs act to reduce the symptoms of MS in mice.

MS is believed to result from increased production of inflammatory immune proteins. This immune activity causes damage to myelin, the substance that
insulates nerve fibers, along with nerve fibers themselves.

"The causes of MS are not completely understood," Feinstein says. "However, it is known that activated lymphocytes in the bloodstream enter the brain, where they produce toxic substances that eventually cause damage to the myelin-forming cells of the brain ((the oligodendrocytes)) and to neurons as well. In addition, once in the brain, the lymphocytes activate resident brain cells that further increase the production of toxic substances."

Feinstein is now designing a clinical trial to test the safety and proper dosage of the drugs in MS patients. He hopes to start that trial within a year.

Even if the drugs are only as good as those currently in use, they still offer an advantage for patients because they can be taken orally.

"The minimum we're hoping for is that they will be as good as any of the existing drugs," Feinstein says. "But there's a possibility they could prove to be better because this is a different class of drugs with different targets and effects."

The study involved collaborations with researchers at several other universities and hospitals, including Dr. Michael Heneka of the University of Bonn in Germany, and was supported by a grant from the National Multiple Sclerosis Society.





 

 

                  

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