Certain B

Primær information

  • Handelsnavn:
  • Certain B Flydende middel
  • Lægemiddelform:
  • Flydende middel
  • Sammensætning:
  • 1000 g/l sprede-klæbemiddel
  • Brugt til:
  • Planter
  • Medicin typen:
  • agrokemiske

Dokumenter

  • for den brede offentlighed:
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    Anmode informationsbrochure for offentligheden.

  • for sundhedspersonale:
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.


    Anmode informationsbrochure for sundhedspersonale.

Lokation

  • Fås i:
  • Certain B Flydende middel
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • SEGES Landbrug & Fødevarer
  • Autorisation status:
  • Udgået
  • Sidste ændring:
  • 08-02-2018
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.

    Anmode informationsbrochure for offentligheden.

23-4-2018

Ziegenfelder Company Recalls Certain Ice Pops For Possible Health Risk

Ziegenfelder Company Recalls Certain Ice Pops For Possible Health Risk

As a precaution, the Ziegenfelder Company of Wheeling, WV is voluntarily recalling approximately 3,000 cases of Budget $aver Cherry Pineapple Monster Pops and Sugar Free Twin Pops because the products have the potential to be contaminated with Listeria monocytogenes. Listeria can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as fever, headache, stiffness, naus...

FDA - U.S. Food and Drug Administration

19-4-2018

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has 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 rare circumstances, infection with Salmonella can result...

FDA - U.S. Food and Drug Administration

19-4-2018

Viable Solutions, LLC Recalls Certain Kratom-Containing Powder Products Because of Possible Health Risk

Viable Solutions, LLC Recalls Certain Kratom-Containing Powder Products Because of Possible Health Risk

Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has 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.

FDA - U.S. Food and Drug Administration

17-4-2018

Certain Implantable Cardiac Devices by Abbott (formerly St. Jude Medical): FDA Safety Communication - Battery Performance Alert and Cybersecurity Firmware Updates

Certain Implantable Cardiac Devices by Abbott (formerly St. Jude Medical): FDA Safety Communication - Battery Performance Alert and Cybersecurity Firmware Updates

If the battery runs out, the ICD or CRT-D will be unable to deliver life-saving pacing or shocks, which could lead to patient death. Posted 04/17/2018

FDA - U.S. Food and Drug Administration

16-4-2018

Women taking birth control pills reminded to return any packages for replacement if the pills are missing or look unusual

Women taking birth control pills reminded to return any packages for replacement if the pills are missing or look unusual

In light of continuing complaints of quality issues involving certain prescription birth control pills, Health Canada is reminding women to check their packages of birth control pills. If you notice anything unusual in the package, such as missing or damaged pills, you should return the package to the pharmacy for replacement as soon as possible. Skipping a dose because the pill is missing, or taking a damaged (for example, chipped or fragmented) pill, may increase the risk of pregnancy because less acti...

Health Canada

11-4-2018

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.

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

Independent Nutrition, Inc Issues Allergy Alert On Undeclared Milk in Ignite Pre-Workout Supplement Products

Independent Nutrition, Inc Issues Allergy Alert On Undeclared Milk in Ignite Pre-Workout Supplement Products

April 5, 2018, Independent Nutrition Inc, dba Back to Health of Eugene, Oregon is recalling certain lots of the Ignite High Endurance Pre-Workout Supplement products because it may contain undeclared milk. People who have an allergy or sever sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

5-4-2018

Recall of Certain Lots of Izzy’s Maple Nut Ice Cream Due to Undeclared Peanuts

Recall of Certain Lots of Izzy’s Maple Nut Ice Cream Due to Undeclared Peanuts

Izzy’s Ice Cream, LLC is voluntarily recalling limited numbers of its Maple Nut Ice Cream pints following a supplier’s recall of walnuts due to the possible presence of undeclared peanut residue. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products

FDA - U.S. Food and Drug Administration

29-3-2018

FDA expands approval of Blincyto for treatment of a type of leukemia in patients who have a certain risk factor for relapse

FDA expands approval of Blincyto for treatment of a type of leukemia in patients who have a certain risk factor for relapse

FDA expands approval of Blincyto for treatment of a type of leukemia in patients who have a certain risk factor for relapse

FDA - U.S. Food and Drug Administration

27-3-2018

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

The authorization classifies integrated continuous glucose monitoring devices in class II and subjects them to certain criteria called special controls

FDA - U.S. Food and Drug Administration

23-3-2018

BD Vacutainer Blood Collection Tubes by Becton, Dickinson and Company (BD): Class I Recall - Chemical Interference with Certain Tests

BD Vacutainer Blood Collection Tubes by Becton, Dickinson and Company (BD): Class I Recall - Chemical Interference with Certain Tests

Falsely lower test results may lead to improper patient management and treatment for lead exposure or poisoning.

FDA - U.S. Food and Drug Administration

23-3-2018

PDX Aromatics Issues Second Expanded Recall of Kratom Products Because of Possible Health Risk

PDX Aromatics Issues Second Expanded Recall of Kratom Products Because of Possible Health Risk

PDX Aromatics, DBA Kraken Kratom, Phytoextractum, and Soul Speciosa, is again expanding the scope of their 3/9/2018 and 3/15/2018 voluntary recalls to include certain red vein and green vein kratom powder and capsule products because they have the potential to be contaminated with Salmonella. The second expanded recall is being initiated in response to additional positive findings of Salmonella associated with PDX Aromatics’ products following the FDA’s investigation.

FDA - U.S. Food and Drug Administration

22-3-2018

BD Updates Instructions for Use for Certain BD Vacutainer® Blood Collection Tubes

BD Updates Instructions for Use for Certain BD Vacutainer® Blood Collection Tubes

BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced it is updating the instructions for use of certain BD Vacutainer® tubes as part of its quality process to ensure that customers understand the appropriate uses of these products.

FDA - U.S. Food and Drug Administration

17-3-2018

PDX Aromatics Expands Recall of Kratom Products Because of Possible Health Risk

PDX Aromatics Expands Recall of Kratom Products Because of Possible Health Risk

PDX Aromatics, DBA Kraken Kratom, Phytoextractum, and Soul Speciosa, is expanding the scope of their 3/9/2018 voluntary recall of certain kratom white vein powder and capsule products and red vein powder products because they have the potential to be contaminated with Salmonella. The expanded recall is being initiated in response to additional positive findings of Salmonella associated with Aromatics' products following the FDA initial investigation.

FDA - U.S. Food and Drug Administration

16-3-2018

Tobacco and related products

Tobacco and related products

The Tobacco Products Directive (2014/40/EU) lays down rules relating to the manufacture, presentation and sale of tobacco and related products (other smoking products, vaping products). While it does not establish a marketing authorisation system, the Directive requires manufacturers and importers to declare these products to the competent authorities of the Member States before they can be marketed. Their composition, emissions, toxicological data on the ingredients, in-depth studies for certain additiv...

France - Agence Nationale du Médicament Vétérinaire

13-3-2018

MAAX Spas Industries Corp. recalls Self-Contained Portable Spas with Delta UV Generator

MAAX Spas Industries Corp. recalls Self-Contained Portable Spas with Delta UV Generator

On certain hot tubs and swim spas equipped with Delta UV model EA-4H-5 generators, moisture can accumulate on the connectors of the generator to the UV bulb, which can lead to an electrical arcing that can cause the unit to catch fire, posing a fire hazard.

Health Canada

10-3-2018

PDX Aromatics Recalls Kratom Powder Because Of Possible Health Risk

PDX Aromatics Recalls Kratom Powder Because Of Possible Health Risk

PDX Aromatics of Portland, Oregon DBA Kraken Kratom, Phytoextractum, and Soul Speciosa, has initiated a recall of certain kratom-containing powder products because it has 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

FDA - U.S. Food and Drug Administration

1-3-2018

Goodman Manufacturing Company, L.P. recalls certain unbranded and Goodman, Amana, and Daikin brand Modular Blowers

Goodman Manufacturing Company, L.P. recalls certain unbranded and Goodman, Amana, and Daikin brand Modular Blowers

The labels found on the serial plate have incorrect electrical information that could result in installers and servicers using undersized wiring or incorrect fuse/circuit breaker parts, posing a fire hazard.

Health Canada

24-2-2018

TruPet, LLC Issues Voluntary Recall of Certain "Treat Me Crunchy Beef Delight" Pet Treats

TruPet, LLC Issues Voluntary Recall of Certain "Treat Me Crunchy Beef Delight" Pet Treats

TruPet, LLC of Milford, OH, is voluntarily recalling a limited amount of Treat Me Crunchy Beef Delight, 2.5oz Pet treats 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

15-2-2018

FDA expands treatment window for use of clot retrieval devices in certain stroke patients

FDA expands treatment window for use of clot retrieval devices in certain stroke patients

FDA expands treatment window for use of clot retrieval devices in certain stroke patient

FDA - U.S. Food and Drug Administration

14-2-2018

FDA approves new treatment for a certain type of prostate cancer using novel clinical trial endpoint

FDA approves new treatment for a certain type of prostate cancer using novel clinical trial endpoint

FDA approves Erleada (apalutamide), first treatment for non-metastatic, castration-resistant prostate cancer

FDA - U.S. Food and Drug Administration

14-2-2018

FDA Investigates Pattern of Contamination in Certain Raw Pet Foods Made by Arrow Reliance Inc., Including Darwin’s Natural Pet Products and ZooLogics Pet Food

FDA Investigates Pattern of Contamination in Certain Raw Pet Foods Made by Arrow Reliance Inc., Including Darwin’s Natural Pet Products and ZooLogics Pet Food

The FDA is alerting pet owners to a history of four recalls of and multiple complaints associated with Darwin’s Natural and ZooLogics pet foods, manufactured by Arrow Reliance Inc., dba Darwin’s Natural Pet Products, over the period from October 17, 2016 to February 10, 2018. In each instance, the company recalled these products after being alerted to positive findings of Salmonella and/or Listeria monocytogenes in samples of their raw pet food products.

FDA - U.S. Food and Drug Administration

13-2-2018

FDA Proposes to Require Electronic Submission of Certain Postmarketing Safety Reports for Approved New Animal Drugs

FDA Proposes to Require Electronic Submission of Certain Postmarketing Safety Reports for Approved New Animal Drugs

FDA proposed a rule to require animal drug sponsors to submit to the agency certain adverse drug experience and product manufacturing defect reports on Form FDA 1932 in electronic format.

FDA - U.S. Food and Drug Administration

8-2-2018

Fujitsu Canada, Inc. recalls Panasonic Battery Packs used in certain Fujitsu personal computers

Fujitsu Canada, Inc. recalls Panasonic Battery Packs used in certain Fujitsu personal computers

The battery can overheat, posing a potential burn and fire hazard.

Health Canada

26-1-2018

FDA approves new treatment for certain digestive tract cancers

FDA approves new treatment for certain digestive tract cancers

FDA approves first radioactive drug for a certain type of digestive tract cancer called GEP-NETs

FDA - U.S. Food and Drug Administration

16-1-2018

Bellisio Foods, Inc. Issues Allergy Alert Regarding Certain Michelina’s Fettuccine Alfredo Packages Due to Potential Presence of Undeclared Soy

Bellisio Foods, Inc. Issues Allergy Alert Regarding Certain Michelina’s Fettuccine Alfredo Packages Due to Potential Presence of Undeclared Soy

Bellisio Foods, Inc., a Jackson, Ohio, manufacturer, is voluntarily recalling certain Michelina’s Fettuccine Alfredo due to the possibility some packages may contain undeclared chicken with soy that is not listed on packaging. People who have an allergy or sensitivity to soy may run the risk of serious allergic reaction(s) if they consume this product.

FDA - U.S. Food and Drug Administration

12-1-2018

FDA approves first treatment for breast cancer with a certain inherited genetic mutation

FDA approves first treatment for breast cancer with a certain inherited genetic mutation

FDA approves first treatment for breast cancer with a certain inherited genetic mutation

FDA - U.S. Food and Drug Administration

4-1-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA Food Safety Modernization Act enforcement discretion guidance

Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA Food Safety Modernization Act enforcement discretion guidance

FDA announced today guidance outlining four key areas that it does not intend to enforce in the FDA Food Safety Modernization Act rules. The provisions relate to the “farm” definition, requirements related to written assurances from a manufacturer’s customers, requirements for importers of food contact substances, and requirements related to certain human food by-products for use as animal food.

FDA - U.S. Food and Drug Administration

2-1-2018

PharMEDium Services, LLC Issues Voluntary Nationwide Recall of Certain Lots of Compounded Sterile Products due to Lack of Sterility Assurance

PharMEDium Services, LLC Issues Voluntary Nationwide Recall of Certain Lots of Compounded Sterile Products due to Lack of Sterility Assurance

December 27, 2017 Lake Forest, IL PharMEDium Services, LLC (PharMEDium) is voluntarily recalling the below lots of drug products to the hospital/user level due to a lack of assurance of sterility. Administration of a drug product intended to be sterile that is not sterile could result in serious infections that may be life-threatening. To date, PharMEDium has not received any reports of complaints related to the products but is issuing this recall out of an abundance of caution following a commitment m...

FDA - U.S. Food and Drug Administration

22-12-2017

FDA updates the label of Tasigna to reflect that certain patients with a type of leukemia may be eligible to stop treatment after sustained response

FDA updates the label of Tasigna to reflect that certain patients with a type of leukemia may be eligible to stop treatment after sustained response

FDA updates the label of Tasigna to reflect that certain patients with a type of leukemia may be eligible to stop treatment after sustained response

FDA - U.S. Food and Drug Administration

22-12-2017

New warnings regarding the use of certain sedative and anesthetic drugs during pregnancy and in early childhood

New warnings regarding the use of certain sedative and anesthetic drugs during pregnancy and in early childhood

OTTAWA – Anesthetics and sedatives are used to prevent pain during surgery and other procedures or tests. However, the use of certain sedative and anesthetic drugs may have an impact on children’s developing brains.

Health Canada

4-4-2018

Babies Given Certain Meds May Have Higher Odds for Allergies Later

Babies Given Certain Meds May Have Higher Odds for Allergies Later

Title: Babies Given Certain Meds May Have Higher Odds for Allergies LaterCategory: Health NewsCreated: 4/2/2018 12:00:00 AMLast Editorial Review: 4/3/2018 12:00:00 AM

US - MedicineNet

14-3-2018

Certain Teens More Likely to Get Hooked on Opioids

Certain Teens More Likely to Get Hooked on Opioids

Title: Certain Teens More Likely to Get Hooked on OpioidsCategory: Health NewsCreated: 3/12/2018 12:00:00 AMLast Editorial Review: 3/13/2018 12:00:00 AM

US - MedicineNet

7-3-2018

Levaquin vs. Keflex

Levaquin vs. Keflex

Levaquin (levofloxacin) and Keflex (cephalexin) are antibiotics used to treat several types of bacterial infections. Keflex is also used before dental procedures in patients identified with certain heart-related conditions to prevent bacterial infections of the heart known as endocarditis. Levaquin and Keflex belong to different antibiotic drug classes. Levaquin is a fluoroquinolone antibiotic and Keflex is a cephalosporin antibiotic.

US - RxList

27-2-2018

Lamictal vs. Abilify

Lamictal vs. Abilify

Lamictal (lamotrigine) and Abilify (aripiprazole) are used to treat bipolar disorders. Lamictal is also used alone or in combination with other anti-seizure medications for treating certain types of seizures. Abilify is also used to treat schizophrenia, mania, depression, bipolar disorders, autistic disorder, and some irritable behavior disorders. Lamictal and Abilify belong to different drug classes. Lamictal is an anticonvulsant (anti-seizure) and Abilify is an antipsychotic.

US - RxList

27-2-2018

Lamictal vs. Neurontin

Lamictal vs. Neurontin

Lamictal (lamotrigine) and Neurontin (gabapentin) are anticonvulsants (anti-seizure drugs) used alone or in combination with other anti-seizure medications for treating certain types of seizures. Neurontin is also used to treat nerve pain caused by shingles (herpes zoster).

US - RxList

27-2-2018

Lamictal vs. Seroquel

Lamictal vs. Seroquel

Lamictal (lamotrigine) and Seroquel (quetiapine) are used to treat bipolar disorders. Lamictal is also used alone or in combination with other anti-seizure medications for treating certain types of seizures. Seroquel is also used to treat schizophrenia and major depression. Lamictal and Seroquel belong to different drug classes. Lamictal is an anticonvulsant and Seroquel is a psychotropic medication (antipsychotic).

US - RxList

14-2-2018

Babies Face Higher SIDS Risk in Certain States

Babies Face Higher SIDS Risk in Certain States

Title: Babies Face Higher SIDS Risk in Certain StatesCategory: Health NewsCreated: 2/12/2018 12:00:00 AMLast Editorial Review: 2/13/2018 12:00:00 AM

US - MedicineNet

8-2-2018

Flagyl vs. Keflex

Flagyl vs. Keflex

Flagyl, Flagyl ER, and Flagyl Injection (metronidazole) and Keflex (cephalexin) are antibiotics used to treat bacterial infections. Keflex is also used before dental procedures in patients identified with certain heart-related conditions to prevent bacterial infections of the heart known as endocarditis. Flagyl and Keflex are different types of antibiotics. Flagyl is a nitroimidazole antibiotic and Keflex is a cephalosporin antibiotic.

US - RxList

5-2-2018

CERTAIN DRI ROLL-ON (Aluminum Chloride) Liquid [Clarion Brands, LLC]

CERTAIN DRI ROLL-ON (Aluminum Chloride) Liquid [Clarion Brands, LLC]

Updated Date: Feb 5, 2018 EST

US - DailyMed

1-2-2018

Cozaar vs. Hyzaar

Cozaar vs. Hyzaar

Cozaar (losartan) and Hyzaar (losartan potassium-hydrochlorothiazide) are prescribed for the treatment of hypertension. Hyzaar is also used to lower the risk of stroke in certain people with heart disease. Cozaar and Hyzaar both contain an angiotensin receptor blocker (ARB), and Hyzaar is a combination medication that also contains a thiazide diuretic (water pill).

US - RxList

31-1-2018

Lasix vs. Aldactone

Lasix vs. Aldactone

Lasix (furosemide) and Aldactone (spironolactone) are used to reduce edema (fluid accumulation) caused by heart, liver or kidney problems, or high blood pressure (hypertension). Lasix may also be used with antihypertensive drugs to control high blood pressure hypertension). Aldactone is also used to reduce edema caused by certain patients with hyperaldosteronism. Lasix and Aldactone belong to different drug classes. Lasix is an anthranilic acid derivative used as a strong loop diuretic and Aldactone is ...

US - RxList

27-1-2018

Will Certain Foods Bolster Brain Health After Stroke?

Will Certain Foods Bolster Brain Health After Stroke?

Title: Will Certain Foods Bolster Brain Health After Stroke?Category: Health NewsCreated: 1/25/2018 12:00:00 AMLast Editorial Review: 1/26/2018 12:00:00 AM

US - MedicineNet

26-1-2018

News and press releases:  Hydroxyethyl-starch solutions for infusion to be suspended – CMDh endorses PRAC recommendation

News and press releases: Hydroxyethyl-starch solutions for infusion to be suspended – CMDh endorses PRAC recommendation

Suspension due to serious risks of kidney injury and death in certain patient populations

Europe - EMA - European Medicines Agency

26-1-2018

Norepinephrine

Norepinephrine

Norepinephrine (Levophed) is indicated for blood pressure control in certain acute hypotensive states (e.g., pheochromocytomectomy, sympathectomy, poliomyelitis, spinal anesthesia, myocardial infarction, septicemia, blood transfusion, and drug reactions).

US - RxList

26-1-2018

Metoclopramide

Metoclopramide

Metoclopramide is used to treat certain conditions of the stomach and intestines. Metoclopramide is used as a short-term treatment (4 to 12 weeks) for persistent heartburn when the usual medicines do not work well enough. It is used mostly for heartburn that occurs after a meal or during the daytime. Treating persistent heartburn can decrease the damage done by stomach acid to the swallowing tube (esophagus) and help healing.

US - RxList

26-1-2018

Octreotide

Octreotide

Octreotide is used to treat severe watery diarrhea and sudden reddening of the face and neck caused by certain types of tumors (e.g., carcinoid tumors, vasoactive intestinal peptide tumors) that are found usually in the intestines and pancreas. The symptoms occur when these tumors make too much of certain natural substances (hormones). This medication works by blocking the production of these hormones. By decreasing watery diarrhea, octreotide helps to reduce the loss of body fluids and minerals.

US - RxList

26-1-2018

Methylphenidate

Methylphenidate

Methylphenidate is used to treat attention deficit hyperactivity disorder - ADHD. It works by changing the amounts of certain natural substances in the brain. Methylphenidate belongs to a class of drugs known as stimulants. It can help increase your ability to pay attention, stay focused on an activity, and control behavior problems. It may also help you to organize your tasks and improve listening skills.

US - RxList

23-1-2018

Risperidone

Risperidone

Risperidone is used to treat certain mental/mood disorders (such as schizophrenia, bipolar disorder, irritability associated with autistic disorder).

US - RxList

22-1-2018

Pramipexole

Pramipexole

pramipexole is used alone or with other medications to treat Parkinson's disease. It can improve your ability to move and can decrease shakiness (tremor), stiffness, slowed movement, and unsteadiness. It may also decrease the number of episodes of not being able to move ("on-off syndrome"). Pramipexole is a dopamine agonist that works by helping to restore the balance of a certain natural substance (dopamine) in the brain.

US - RxList

22-1-2018

Rituximab

Rituximab

Rituximab is used alone or with other medications to treat certain types of cancer (e.g., non-Hodgkin's lymphoma, chronic lymphocytic leukemia). It is a type of medication called a monoclonal antibody. It works by attaching to certain blood cells from your immune system (B cells) and killing them. It is also used with other monoclonal antibodies and radioactive drugs to treat certain cancers.

US - RxList

18-1-2018

Propafenone

Propafenone

Propafenone is used to treat certain types of serious (possibly fatal) irregular heartbeat (such as paroxysmal supraventricular tachycardia and atrial fibrillation). It is used to restore normal heart rhythm and maintain a regular, steady heartbeat. Propafenone is known as an anti-arrhythmic drug.

US - RxList

12-1-2018

FDA Approves Lynparza for Breast Cancer with Genetic Mutation

FDA Approves Lynparza for Breast Cancer with Genetic Mutation

FDA approves first treatment for breast cancer with a certain inherited genetic mutation.

US - RxList

11-1-2018

Infliximab (Remicade)

Infliximab (Remicade)

Infliximab is used to treat certain types of arthritis (rheumatoid arthritis, arthritis of the spine, psoriatic arthritis), certain bowel diseases (Crohn's disease, ulcerative colitis), and a certain severe skin disease (chronic plaque psoriasis).

US - RxList

11-1-2018

Sulfasalazine

Sulfasalazine

Sulfasalazine is used to treat a certain type of bowel disease called ulcerative colitis

US - RxList

4-1-2018

Lamictal vs. Trileptal

Lamictal vs. Trileptal

Lamictal (lamotrigine) and Trileptal (oxcarbazepine) are antiepileptic drugs (AEDs), also called anticonvulsants, used alone or in combination with other antiseizure medications for treating certain types of seizures.

US - RxList

4-1-2018

Vardenafil

Vardenafil

Vardenafil is an erectile dysfunction drug that works by blocking a certain enzyme (phosphodiesterase-PDE5) used to treat erectile dysfunction (impotence).

US - RxList

3-1-2018

For Five Cancers, Screening Skews Risk Factors

For Five Cancers, Screening Skews Risk Factors

Screening and diagnostic testing can affect the incidence of certain cancers and result in "self-fulfilling" risk factors associated with those cancers, according to a new essay by two major figures in the US cancer scene.

US - RxList

3-1-2018

Methylprednisolone

Methylprednisolone

Methylprednisolone is used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/kidney/intestinal/lung diseases, and immune system disorders. It decreases your immune system's response to various diseases to reduce symptoms such as swelling, pain, and allergic-type reactions. This medication is a corticosteroid hormone.

US - RxList

3-1-2018

Lamictal vs. Depakote

Lamictal vs. Depakote

Lamictal (lamotrigine) and Depakote (divalproex sodium) are antiepileptic drugs (AEDs), also called anticonvulsants, used alone or in combination with other antiseizure medications for treating certain types of seizures.

US - RxList

3-1-2018

Lamictal vs. Keppra

Lamictal vs. Keppra

Lamictal (lamotrigine) and Keppra (levetiracetam) are anti-epileptic drugs (AEDs) (anticonvulsants) used alone or in combination with other antiseizure medications for treating certain types of seizures.

US - RxList

28-12-2017

CERTAIN DRI SOLID (Aluminum Sesquichlorohydrate) Stick [Clarion Brands, LLC]

CERTAIN DRI SOLID (Aluminum Sesquichlorohydrate) Stick [Clarion Brands, LLC]

Updated Date: Dec 28, 2017 EST

US - DailyMed

23-12-2017

Boxed Warning Removed From Certain Asthma Medications: FDA

Boxed Warning Removed From Certain Asthma Medications: FDA

Title: Boxed Warning Removed From Certain Asthma Medications: FDACategory: Health NewsCreated: 12/21/2017 12:00:00 AMLast Editorial Review: 12/22/2017 12:00:00 AM

US - MedicineNet