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"MediGuard flagged a potential conflict between two of my meds. I took these details to my GP and after some dosage changes we were able to relieve some of the side effects." —UK Male with Asthma, Age 34
"I received an email from MediGuard to let me know that the syringes that I was using at that time, could be part of a recall. I followed the links...and found out that the syringes that I was using, were indeed part of the recall. If I had not received that email, I may have been at danger of the syringe breaking off inside me." —US Female with Diabetes, Age 44
"MediGuard has told me of interactions with certain medicines and when I mentioned this to GP [general practitioner] he changed it accordingly, preventing all the drowsiness I used to have." —UK Female, Age 46
"I started to get pain in my upper arm muscles and found that two of my prescription medicines react to each other to produce the pain and a weakening of the muscles. I took the information to my doctor who then took me off one of the medicines." —UK Male, Age 58
"I'm on so many medications that I can't remember them all...MediGuard makes it so easy to just pull out my [medication] card & hand it to my doctor for them to review. I keep that card with my Drivers license in case I ever get in an accident & cannot speak." —US Female with Bipolar Disorder, Age 49
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Recent Alerts

FDA Makes Changes to Risk Evaluation and Mitigation Strategies (REMS) Program for Nplate (Romiplostim) and Promacta (Eltrombopag)

2012-01-26

The U.S. Food and Drug Administration (FDA) has approved changes to the Risk Evaluation and Mitigation Strategies (REMS) for platelet-booster drugs Nplate (romiplostim) injection and Promacta (eltromb... More

FDA Announces New Risk Factor for Progressive Multifocal Leukoencephalopathy (PML) Associated with Tysabri (Natalizumab)

2012-01-24

The U.S. Food and Drug Administration (FDA) is informing the public that testing positive for anti-JC virus (JCV) antibodies has been identified as a risk factor for progressive multifocal leukoenceph... More

Rexall, Inc Issues Allergy Alert and Recall of Single Lot of Calcium 1200mg plus Vitamin D 1000 IU Softgels

2012-01-18

Rexall, Inc., of Deerfield Beach, Florida, has announced a recall of Rexall brand Calcium 1200 mg plus 1000 IU Vitamin D3, 60 softgels. The affected bottles actually contain a TABLET product, Triple S... More

New Study Raises Concerns about Daily Aspirin Use in People Without a History of Heart Disease

2012-01-18

A new study published in the Archives of Internal Medicines highlights safety concerns about aspirin use by people without a history of heart disease. The subjects in this study who had never had a he... More

New Boxed Warning for Progressive Multifocal Leukoencephalopathy (PML) and Contraindication for Adcetris (Brentuximab vedotin)

2012-01-16

The U.S. Food and Drug Adminstration has announced that two additional cases of progressive multifocal leukoencephalopathy (PML), a rare but serious brain infection that can result in death, have been... More


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DISCLAIMER: MediGuard is not intended to be a substitute for professional medical advice. MediGuard cannot and does not take into consideration every possible interaction or account for individual responses to medicine. Different individuals may respond to medication in different ways. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective, or appropriate for any given patient. Always seek the advice of a qualified health provider with any questions you may have before making any changes to your treatment. The use of the MediGuard site and its content is at your own risk. The MediGuard site and the information contained in it is intended for users in the United States and information in other countries may be different.

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