EVADAY (FOOD)

Main information

  • Trade name:
  • EVADAY (FOOD) 10 CAP
  • Pharmaceutical form:
  • CAP
  • Composition:
  • 10
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • EVADAY (FOOD) 10 CAP
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

19-4-2018

Superior Foods Company Voluntarily Recalls 487 lbs. of Smoked Salmon Spreads

Superior Foods Company Voluntarily Recalls 487 lbs. of Smoked Salmon Spreads

Superior Foods Company located in Kentwood, Michigan is voluntarily recalling a specific lot of Smoked Salmon Spreads (487 lbs.) that were produced on March 26, 2018. This voluntary action is being undertaken in cooperation with the U.S. Food and Drug Administration and the Michigan Department of Agriculture and Rural Development.

FDA - U.S. Food and Drug Administration

18-4-2018

The impact of global change on the emergence of plant diseases and pests in Europe

The impact of global change on the emergence of plant diseases and pests in Europe

The French Agency for Food, Environmental and Occupational Health and Safety (ANSES), in collaboration with the European Food Safety Authority (EFSA) and the European and Mediterranean Plant Protection Organization (EPPO), is organising a conference on 23-24 April 2018 in Paris. This two-day event will review the current state of scientific knowledge worldwide and provide a forum for sharing experiences on the reasons for the emergence of plant diseases and pests, as well as their impact on the environme...

France - Agence Nationale du Médicament Vétérinaire

18-4-2018

Carnivore Meat Company Issues Voluntary Recall of limited batches of “Vital Essentials® Freeze-Dried Beef Toppers” and “Vital Essentials® Frozen Beef Chub Entrée for Dogs” Pet Food

Carnivore Meat Company Issues Voluntary Recall of limited batches of “Vital Essentials® Freeze-Dried Beef Toppers” and “Vital Essentials® Frozen Beef Chub Entrée for Dogs” Pet Food

Carnivore Meat Company of Green Bay, WI, is voluntarily recalling a limited amount of pet food because the products may have the potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

17-4-2018

Statement by Dr. Susan Mayne on FDA efforts to reduce consumer exposure to arsenic in rice

Statement by Dr. Susan Mayne on FDA efforts to reduce consumer exposure to arsenic in rice

One way FDA oversees food safety is through monitoring of contaminants in food, such as arsenic, assessing potential exposure and taking steps to reduce exposure

FDA - U.S. Food and Drug Administration

16-4-2018

Vitakraft Sun Seed Recalls of Sunseed Vita Prima Sugar Glider Food Due to Possible <em>Salmonella</em> Health Risk

Vitakraft Sun Seed Recalls of Sunseed Vita Prima Sugar Glider Food Due to Possible <em>Salmonella</em> Health Risk

Vitakraft Sun Seed Inc. of Weston, OH, is voluntarily recalling one lot of Sunseed Vita Prima Exotics Sugar Glider Formula because it has the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

FDA - U.S. Food and Drug Administration

15-4-2018

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd is voluntarily recalling four batches of the K9 Natural Frozen Chicken Feast 2.2lb and 11lb bags that was imported into the US market in June 2017 because they have the potential to be contaminated with Listeria Monocytogenes.

FDA - U.S. Food and Drug Administration

14-4-2018

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

R.J. Reynolds Vapor Company has voluntarily initiated a nationwide safety recall of all Vuse Vibe power units. The Company initiated the recall after receiving consumer complaints about malfunctioning batteries, which may cause the power unit to overheat and create a fire risk. The Company notified the U.S. Food and Drug Administration regarding the issue and will be working directly with the Agency on this voluntary recall.

FDA - U.S. Food and Drug Administration

13-4-2018

FDA takes step to protect consumers against dietary supplements containing dangerously high levels of extremely concentrated or pure caffeine

FDA takes step to protect consumers against dietary supplements containing dangerously high levels of extremely concentrated or pure caffeine

Today, the U.S. Food and Drug Administration took an important step to better protect consumers from the dangers of highly concentrated and pure caffeine products.

FDA - U.S. Food and Drug Administration

13-4-2018

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group, Inc., of Miami, FL, is voluntarily recalling its ten-ounce packages of La Marinera Brand Dried Yellow Potatoes because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

11-4-2018

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

Under the national nutrivigilance scheme, reports of adverse effects likely to be associated with the consumption of food supplements containing melatonin have been brought to the attention of ANSES. A retrospective analysis of these reports, combined with the considerable level of consumption of this type of supplement, led ANSES to conduct an assessment of the potential health risks.

France - Agence Nationale du Médicament Vétérinaire

6-4-2018

Aspire Food Group Issues Alert on Undeclared Sulfites in Exo Bars

Aspire Food Group Issues Alert on Undeclared Sulfites in Exo Bars

Aspire Food Group of Austin, TX, is recalling its 60 gram bars of EXO Blueberry Vanilla, Peanut Butter & Jelly, and Apple Cinnamon bars because they may contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reaction if they consume these products.

FDA - U.S. Food and Drug Administration

5-4-2018

Exposure to silver nanoparticles

Exposure to silver nanoparticles

Silver nanoparticles are used in various industrial applications, in sectors such as food (additives, food packaging, internal linings of refrigerators), textiles (clothing and bedding) and cosmetic and hygiene products (toothbrushes, hair straighteners, disinfectant sprays, etc.). They are mainly used for their antibacterial and antifungal properties. However, it is still proving very difficult to obtain an inventory referencing all products containing silver nanoparticles in France and elsewhere in the...

France - Agence Nationale du Médicament Vétérinaire

3-4-2018

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

3-4-2018

FDA orders mandatory recall for kratom products due to risk of salmonella

FDA orders mandatory recall for kratom products due to risk of salmonella

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

2-4-2018

New York raw milk cheese company ordered to stop sales for food safety violations

New York raw milk cheese company ordered to stop sales for food safety violations

FDA announces an enforcement action taken against Vulto Creamery of New York. The company cannot sell ready-to-eat raw cheese product until it complies with the consent decree. Vulto was linked to an outbreak last year.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Black Lion Pill contains hidden drug ingredient

Public Notification: Black Lion Pill contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Black Lion Pill, a product promoted and sold for sexual enhancement on various websites, including www.rakuten.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Rhino 69 Extreme 50000, a product promoted and sold for sexual enhancement on various websites, including www.bonanza.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Red Zone Xtreme 3000, a product promoted and sold for sexual enhancement on various websites, including www.ebay.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Foot-and-mouth disease: a new international reference mandate for ANSES

Foot-and-mouth disease: a new international reference mandate for ANSES

Through its Maisons-Alfort Laboratory for Animal Health, ANSES has just been appointed Reference Centre of the Food and Agriculture Organisation of the United Nations (FAO) for foot-and-mouth disease and vesicular diseases. This new mandate expands the reference activities of the Maisons-Alfort Laboratory for Animal Health regarding foot-and-mouth disease, particularly in the context of its reference mandates at a national, European and international level, and is recognition of ANSES's commitment to add...

France - Agence Nationale du Médicament Vétérinaire

26-3-2018

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef of Eatonton, GA, is voluntarily recalling lot#GA0131 of BRB Complete raw pet food because of the potential of contamination with Salmonella and Listeria monocytogenes. The cause of the recall: This recall was initiated after samples collected and tested by the FDA showed positive for Salmonella and Listeria monocytogenes. There has been no consumer or pet illnesses in association with this product. Blue Ridge Beef is voluntarily recalling this product lot as a commitment to consumer and p...

FDA - U.S. Food and Drug Administration

26-3-2018

Mrs. Gerry’s Kitchen Issues Allergen Alert on Undeclared Seafood in Salad

Mrs. Gerry’s Kitchen Issues Allergen Alert on Undeclared Seafood in Salad

The salads may contain undeclared traces of imitation crab meat. People who have allergies to fish or shell fish run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled salad was shipped to retail and food service distributers in IL, IA, KS, MI, MN, MT, NE, ND, SD, UT, and WI. No illnesses have been reported to date in connection with this problem.

FDA - U.S. Food and Drug Administration

21-3-2018

5 Things to Know About Breast Implants

5 Things to Know About Breast Implants

The U.S. Food and Drug Administration regulates breast implants as medical devices. Learn about the risks of these products, and consider this advice.

FDA - U.S. Food and Drug Administration

20-3-2018

Radagast Pet Food, Inc. Voluntarily Recalls One Lot of Rad Cat Raw Diet Free-Range Chicken and One Lot of Free-Range Turkey Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. Voluntarily Recalls One Lot of Rad Cat Raw Diet Free-Range Chicken and One Lot of Free-Range Turkey Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. of Portland, OR is recalling one lot of Free-Range Chicken and one lot of Free-Range Turkey Recipe because they have the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

FDA - U.S. Food and Drug Administration

19-3-2018

Natural Grocers Issues Recall on Coconut Smiles Organic Due to <em>Salmonella</em>

Natural Grocers Issues Recall on Coconut Smiles Organic Due to <em>Salmonella</em>

Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado-based natural grocery chain, is recalling Natural Grocers brand 10-ounce Coconut Smiles Organic due to the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rar...

FDA - U.S. Food and Drug Administration

17-3-2018

Oregon Food Bank Voluntarily Recalls Nutritional Yeast

Oregon Food Bank Voluntarily Recalls Nutritional Yeast

Oregon Food Bank is voluntarily recalling 1,219 pounds of nutritional yeast, which was donated to the food bank. No illness has been reported but it was donated at the same time as two other recalled products -- chia and pumpkin seeds.

FDA - U.S. Food and Drug Administration

17-3-2018

Oregon Food Bank Voluntarily Recalls Pumpkin Seeds Because Of Possible Contamination By Listeria Species

Oregon Food Bank Voluntarily Recalls Pumpkin Seeds Because Of Possible Contamination By Listeria Species

As a result of the ongoing recall of donated chia seeds that began on March 12, 2018, Oregon Food Bank has initiated a voluntary recall of 63,825 pounds of pumpkin seeds received on the same donation. These donated pumpkin seeds have the potential to be contaminated with Listeria species.

FDA - U.S. Food and Drug Administration

16-3-2018

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer is voluntarily recalling Alka-Seltzer Plus® packages that: • Were sold only in the U.S. at Walmart, CVS, Walgreens and Kroger (including Dillons Food Stores, Fred Meyer, Fry’s Food Stores, Ralphs, King Soopers and Smith’s Food and Drug) after February 9, 2018. • Can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall (please see attached photos). The affected...

FDA - U.S. Food and Drug Administration

13-3-2018

Oregon Food Bank Issues Alert on Foreign Material in Chia Seeds

Oregon Food Bank Issues Alert on Foreign Material in Chia Seeds

Oregon Food Bank of Portland, Oregon has initiated a Class II recall of 22,201 pounds of chia seeds, which were donated to the food bank. The product may be contaminated with rodent droppings. While no known illnesses have been associated with this product, use or consumption may present a health hazard to consumers.

FDA - U.S. Food and Drug Administration

12-3-2018

Wegmans Food Markets Issues Allergen Alert on Undeclared Egg in Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. Sold in the Sushi Department

Wegmans Food Markets Issues Allergen Alert on Undeclared Egg in Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. Sold in the Sushi Department

Wegmans Food Markets, Inc. is recalling Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. (UPC7-66630-98023) with a best-by of 7/4/18 or 7/5/18 because the product may contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

12-3-2018

ANSES and INRA renew their partnership for five more years

ANSES and INRA renew their partnership for five more years

In the presence of Bruno Le Maire, Minister of the Economy and Finance, Stéphane Travert, Minister of Agriculture and Food, and Brune Poirson, Secretary of State to the Minister for Ecological and Inclusive Transition, Roger Genet, Director General of ANSES, and Philippe Mauguin, President of the National Institute of Agronomic Research (INRA), have renewed the partnership framework agreement between the two organisations for five years. Language English

France - Agence Nationale du Médicament Vétérinaire

12-3-2018

Traces of chemical contaminants in food – three questions for Roger Genet

Traces of chemical contaminants in food – three questions for Roger Genet

Roger Genet, Director General of ANSES, considers the issue of chemical contaminants in fruit and vegetables, which does not necessarily translate into a risk for the consumer. He explains how the Agency goes about monitoring the presence of pesticide residues in food, assessing the exposure of different population groups and ensuring consumer protection.   Language English

France - Agence Nationale du Médicament Vétérinaire

8-3-2018

FDA Drug Safety Communication: FDA updates warnings for oral and injectable fluoroquinolone antibiotics due to disabling side effects

FDA Drug Safety Communication: FDA updates warnings for oral and injectable fluoroquinolone antibiotics due to disabling side effects

[07-26-2016] The U.S. Food and Drug Administration (FDA) approved changes to the labels of fluoroquinolone antibacterial drugs for systemic use (i.e., taken by mouth or by injection).

FDA - U.S. Food and Drug Administration

8-3-2018

FDA Drug Safety Communication: FDA warns about serious bleeding risk with over-the-counter antacid products containing aspirin

FDA Drug Safety Communication: FDA warns about serious bleeding risk with over-the-counter antacid products containing aspirin

[06-06-2016] The U.S. Food and Drug Administration (FDA) is warning consumers about the risk of serious bleeding when using nonprescription, also known as over-the-counter or OTC, aspirin-containing antacid products to treat heartburn, sour stomach, acid indigestion, or upset stomach.

FDA - U.S. Food and Drug Administration

7-3-2018

Weis Markets Expands Allergy Alert for Weis Quality Dried Beef Party Rye Dip Sold in 11 Stores Due to Undeclared Milk and Egg Allergen

Weis Markets Expands Allergy Alert for Weis Quality Dried Beef Party Rye Dip Sold in 11 Stores Due to Undeclared Milk and Egg Allergen

Weis Markets today announced it has expanded its recall for its store-made Weis Quality Dried Beef Party Rye dip for failing to list egg and milk allergens on its label. Food allergies are an immune system reaction that occurs soon after eating a food containing an allergen.

FDA - U.S. Food and Drug Administration

6-3-2018

FDA Drug Safety Communication: FDA warns about cases of rare brain infection with MS drug Gilenya (fingolimod) in two patients with no prior exposure to immunosuppressant drugs

FDA Drug Safety Communication: FDA warns about cases of rare brain infection with MS drug Gilenya (fingolimod) in two patients with no prior exposure to immunosuppressant drugs

[07-04-2015] The U.S. Food and Drug Administration is warning that a case of definite progressive multifocal leukoencephalopathy (PML) and a case of probable PML have been reported in patients taking Gilenya (fingolimod) for multiple sclerosis (MS).

FDA - U.S. Food and Drug Administration

5-3-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s commitment to modernizing food and nutrition programs

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s commitment to modernizing food and nutrition programs

FDA announces commitment to modernize and streamline our food and nutrition programs to make sure that our investments of new and existing resources achieve their intended public health goals.

FDA - U.S. Food and Drug Administration

5-3-2018

FDA Drug Safety Communication: FDA review found no increased cardiovascular risks with Parkinson’s disease drug entacapone

FDA Drug Safety Communication: FDA review found no increased cardiovascular risks with Parkinson’s disease drug entacapone

[10-26-2015] A Food and Drug Administration (FDA) safety review has found no clear evidence of an increased risk of heart attacks, stroke, or other cardiovascular events associated with the use of entacapone for the treatment of Parkinson’s disease.

FDA - U.S. Food and Drug Administration

3-3-2018

Steve’s Real Food Voluntarily Recalls Raw Frozen Dog Food Turkey Canine Recipe Due to Possible <em>Salmonella</em> Contamination

Steve’s Real Food Voluntarily Recalls Raw Frozen Dog Food Turkey Canine Recipe Due to Possible <em>Salmonella</em> Contamination

Steve’s Real Food of Salt Lake City, Utah is voluntarily recalling one lot of 5lb Raw Frozen Dog Food Turkey Canine Recipe due to their potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

2-3-2018

Blue Ridge Beef Recalls Kitten Grind Raw Pet Food Lot#GA1102 Because of Possible Contamination

Blue Ridge Beef Recalls Kitten Grind Raw Pet Food Lot#GA1102 Because of Possible Contamination

Blue Ridge Beef of Eatonton, GA, is recalling lot#GA1102 of Kitten Grind raw pet food because of the potential of contamination with Salmonella and Listeria monocytogenes.

FDA - U.S. Food and Drug Administration

1-3-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s new efforts to advance implementation of the new consumer Nutrition Facts label for foods

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s new efforts to advance implementation of the new consumer Nutrition Facts label for foods

Americans rely on the U.S. Food and Drug Administration to ensure that food labels contain updated nutritional information to help them make more informed food choices that lead to better health for themselves and their families. I’ve made nutrition one of my top priorities, and ensuring that consumers have accurate and science-based information concerning the link between diet and chronic diseases like diabetes, obesity and heart disease is part of that commitment. We need to advance new ways to use the...

FDA - U.S. Food and Drug Administration

26-2-2018

Carnivore Meat Company Issues Voluntary Recall of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” Pet Food

Carnivore Meat Company Issues Voluntary Recall of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” Pet Food

Carnivore Meat Company of Green Bay, WI, is voluntarily recalling a limited amount, 73 cases, of “Vital Essentials Freeze-Dried Beef Nibblets Entrée for Dogs” pet food because the products have the potential to be contaminated with Salmonella. The recall includes only the product listed below.

FDA - U.S. Food and Drug Administration

26-2-2018

FDA Drug Safety Communication: FDA determines 2013 labeling adequate to manage risk of retinal abnormalities, potential vision loss, and skin discoloration with anti-seizure drug Potiga (ezogabine); requires additional study

FDA Drug Safety Communication: FDA determines 2013 labeling adequate to manage risk of retinal abnormalities, potential vision loss, and skin discoloration with anti-seizure drug Potiga (ezogabine); requires additional study

[06-16-2015] Based on reviews of additional safety reports from patients treated with the anti-seizure drug Potiga (ezogabine), the U.S. Food and Drug Administration (FDA) has determined that the potential risks of vision loss due to pigment changes in the retina and of skin discoloration can be adequately managed by following the current recommendations in the Potiga labeling.

FDA - U.S. Food and Drug Administration

26-2-2018

FDA Drug Safety Communication: FDA requires label warnings to prohibit sharing of multi-dose diabetes pen devices among patients

FDA Drug Safety Communication: FDA requires label warnings to prohibit sharing of multi-dose diabetes pen devices among patients

[2-25-2015] In an effort to reduce the serious risk of infection spread through sharing of multi-dose diabetes pen devices intended for single patient use only, the U.S. Food and Drug Administration (FDA) is requiring additional label warnings prohibiting sharing of these injectable medicines.

FDA - U.S. Food and Drug Administration

26-2-2018

FDA Drug Safety Communication: FDA approves label changes for asthma drug Xolair (omalizumab), including describing slightly higher risk of heart and brain adverse events

FDA Drug Safety Communication: FDA approves label changes for asthma drug Xolair (omalizumab), including describing slightly higher risk of heart and brain adverse events

[9-26-2014] A U.S. Food and Drug Administration (FDA) review of safety studies suggests a slightly increased risk of problems involving the heart and blood vessels supplying the brain among patients being treated with the asthma drug Xolair (omalizumab) than in those who were not treated with Xolair. As a result, we have added information about these potential risks to the drug label.

FDA - U.S. Food and Drug Administration

26-2-2018

FDA Drug Safety Communication: FDA study of Medicare patients finds risks lower for stroke and death but higher for gastrointestinal bleeding with Pradaxa (dabigatran) compared to warfarin

FDA Drug Safety Communication: FDA study of Medicare patients finds risks lower for stroke and death but higher for gastrointestinal bleeding with Pradaxa (dabigatran) compared to warfarin

[05-13-2014] In its ongoing review of the blood thinner Pradaxa (dabigatran), the U.S. Food and Drug Administration (FDA) recently completed a new study in Medicare patients comparing Pradaxa to an older blood thinner, warfarin, for risk of ischemic or clot-related stroke, bleeding in the brain, major gastrointestinal (GI) bleeding, myocardial infarction (MI), and death.

FDA - U.S. Food and Drug Administration

20-4-2018

FDA Panel Unanimously Backs Cannabis Drug for Severe Epilepsy

FDA Panel Unanimously Backs Cannabis Drug for Severe Epilepsy

A US Food and Drug Administration (FDA) advisory committee has voted unanimously to support approval of a purified formulation of cannabidiol (Epidiolex, GW Pharmaceuticals) as an adjunctive treatment for Lennox-Gastaut syndrome (LGS) and Dravet syndrome (DS) in patients 2 years of age or older.

US - RxList

16-4-2018

FDA Takes Steps Against Dietary Supplements Containing Dangerously High Levels of Pure Caffeine

FDA Takes Steps Against Dietary Supplements Containing Dangerously High Levels of Pure Caffeine

Today, the U.S. Food and Drug Administration took an important step to better protect consumers from the dangers of highly concentrated and pure caffeine products. These products present a significant public health threat because of the high risk that they will be erroneously used at excessive, potentially dangerous doses. Highly concentrated and pure caffeine, often sold in bulk packages, have been linked to at least two deaths in otherwise healthy individuals.

US - RxList

11-4-2018

FDA OKs First Transitional Contacts That Darken in Sunlight

FDA OKs First Transitional Contacts That Darken in Sunlight

The first contact lenses that have an additive that automatically darkens the lenses when exposed to bright light have been cleared by the US Food and Drug Administration (FDA).

US - RxList

3-4-2018

FDA to Move Ahead With Obama Administration Food Labeling Rules

FDA to Move Ahead With Obama Administration Food Labeling Rules

Title: FDA to Move Ahead With Obama Administration Food Labeling RulesCategory: Health NewsCreated: 3/30/2018 12:00:00 AMLast Editorial Review: 4/2/2018 12:00:00 AM

US - MedicineNet

3-4-2018

Health Tip: Keep Pet Food Safe

Health Tip: Keep Pet Food Safe

Title: Health Tip: Keep Pet Food SafeCategory: Health NewsCreated: 4/2/2018 12:00:00 AMLast Editorial Review: 4/2/2018 12:00:00 AM

US - MedicineNet

2-4-2018

CALAMINE (Ferric Oxide Red) Lotion [Wakefern Food Corp]

CALAMINE (Ferric Oxide Red) Lotion [Wakefern Food Corp]

Updated Date: Apr 2, 2018 EST

US - DailyMed

2-4-2018

LAXATIVE GENTLE (Bisacodyl) Tablet, Sugar Coated [SAVE-A-LOT FOOD STORES, LTD.]

LAXATIVE GENTLE (Bisacodyl) Tablet, Sugar Coated [SAVE-A-LOT FOOD STORES, LTD.]

Updated Date: Apr 2, 2018 EST

US - DailyMed

2-4-2018

DRY SCALP CARE (Pyrithione Zinc) Shampoo [Wakefern Food Corp]

DRY SCALP CARE (Pyrithione Zinc) Shampoo [Wakefern Food Corp]

Updated Date: Apr 2, 2018 EST

US - DailyMed

31-3-2018

Unhealthy Phthalate Chemicals Found in Restaurant Food

Unhealthy Phthalate Chemicals Found in Restaurant Food

Title: Unhealthy Phthalate Chemicals Found in Restaurant FoodCategory: Health NewsCreated: 3/29/2018 12:00:00 AMLast Editorial Review: 3/30/2018 12:00:00 AM

US - MedicineNet

28-3-2018

Sports 'Sponsorships' Hawk Junk Food to Kids

Sports 'Sponsorships' Hawk Junk Food to Kids

Title: Sports 'Sponsorships' Hawk Junk Food to KidsCategory: Health NewsCreated: 3/26/2018 12:00:00 AMLast Editorial Review: 3/27/2018 12:00:00 AM

US - MedicineNet

28-3-2018

FDA Panel Backs Approval of Lofexidine for Opioid Withdrawal

FDA Panel Backs Approval of Lofexidine for Opioid Withdrawal

A US Food and Drug Administration (FDA) advisory committee has recommended approval of lofexidine hydrochloride, a nonopioid, for the mitigation of symptoms in the setting of abrupt opioid withdrawal.

US - RxList

22-3-2018

School Nurses at Ground Zero for Food Allergies

School Nurses at Ground Zero for Food Allergies

Title: School Nurses at Ground Zero for Food AllergiesCategory: Health NewsCreated: 3/20/2018 12:00:00 AMLast Editorial Review: 3/21/2018 12:00:00 AM

US - MedicineNet

22-3-2018

Just How Safe Is Your Pet's Food?

Just How Safe Is Your Pet's Food?

Title: Just How Safe Is Your Pet's Food?Category: Health NewsCreated: 3/21/2018 12:00:00 AMLast Editorial Review: 3/21/2018 12:00:00 AM

US - MedicineNet

20-3-2018

WEGMANS ALOE AND VITAMIN E (Benzalkonium Chloride) Cloth [Wegmans Food Markets Inc.]

WEGMANS ALOE AND VITAMIN E (Benzalkonium Chloride) Cloth [Wegmans Food Markets Inc.]

Updated Date: Mar 20, 2018 EST

US - DailyMed

16-3-2018

Scientific guideline:  Public consultation concerning a request for CVMP opinion under Article 30(3) of Regulation (EC) No 726/2004 on the risk for the consumer resulting from the use of diethanolamine as an excipient in veterinary medicinal products for

Scientific guideline: Public consultation concerning a request for CVMP opinion under Article 30(3) of Regulation (EC) No 726/2004 on the risk for the consumer resulting from the use of diethanolamine as an excipient in veterinary medicinal products for

The European Medicines Agency is seeking stakeholder input on any information or data that may help its Committee for Medicinal Products for Veterinary Use (CVMP) to reach an opinion on consumer risk from using diethanolamine as an excipient in veterinary medicines for food-producing animals.

Europe - EMA - European Medicines Agency

16-3-2018

FDA to Lower Nicotine in Cigarettes to 'Nonaddictive' Levels

FDA to Lower Nicotine in Cigarettes to 'Nonaddictive' Levels

The US Food and Drug Administration (FDA) is taking what it calls a historic first step toward eliminating cigarettes' addictive properties by seeking comments on the impact of lower nicotine levels, how lowering of nicotine levels might be accomplished, and whether doing so might have unintended consequences.

US - RxList

6-3-2018

DAILY MOISTURIZING (Dimethicone) Lotion [Wakefern Food Corp]

DAILY MOISTURIZING (Dimethicone) Lotion [Wakefern Food Corp]

Updated Date: Mar 6, 2018 EST

US - DailyMed

5-3-2018

HAND WASH (Benzalkonium Chloride) Soap [Wakefern Food Corp]

HAND WASH (Benzalkonium Chloride) Soap [Wakefern Food Corp]

Updated Date: Mar 5, 2018 EST

US - DailyMed