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Сепротин 500 IU

Основна информация

  • Търговско наименование:
  • Сепротин 500 IU (Ceprotin 500 IU)
  • Предлага се от:
  • Baxter AG
  • дозиране:
  • 500 IU + 5 ml x 1
  • Лекарствена форма:
  • прах и разтворител за инфузионен разтвор
  • Композиция:
  • прах и разтворител за инфузионен разтвор 500 IU + 5 ml x 1
  • Използвай за:
  • Хората
  • Вид на лекарството:
  • алопатични наркотици
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Документи

Локализация

  • Предлага се в:
  • Сепротин 500 IU (Ceprotin 500 IU)
    България
  • Език:
  • български

Друга информация

Състояние

  • Източник:
  • Изпълнителна агенция по лекарствата - Bulgarian Drug Agency - Bulgaria
  • Последна актуализация:
  • 09-08-2016

24-11-2017

Sun Pharmaceutical Industries Inc. Issues Voluntary Nationwide Recall of Riomet® (Metformin Hydrochloride Oral Solution) Manufactured by a Contract Manufacturer due to Microbial Contamination

Sun Pharmaceutical Industries Inc. Issues Voluntary Nationwide Recall of Riomet® (Metformin Hydrochloride Oral Solution) Manufactured by a Contract Manufacturer due to Microbial Contamination

Sun Pharmaceutical Industries, Inc. (SPII), a wholly owned subsidiary of Sun Pharmaceutical Industries Ltd. (Reuters: SUN.BO, Bloomberg: SUNP IN, NSE: SUNPHARMA, BSE: 524715, “Sun Pharma” including its subsidiaries and/or associate companies) is voluntarily recalling two lots of Riomet® (Metformin Hydrochloride Oral Solution), 500 mg/5mL, to the retail level (Class II Recall). This product is manufactured for SPII by a contract manufacturer. The Riomet® (Metformin Hydrochloride Oral Solution) has been fo...

FDA - U.S. Food and Drug Administration

25-9-2017

FDA conducts major global operation to protect consumers from potentially dangerous prescription drugs sold online

FDA conducts major global operation to protect consumers from potentially dangerous prescription drugs sold online

The U.S. Food and Drug Administration, in partnership with international regulatory and law enforcement agencies, recently took action against more than 500 websites that illegally sell potentially dangerous, unapproved versions of prescription medicines, including opioids, antibiotics and injectable epinephrine products to American consumers.

FDA - U.S. Food and Drug Administration

25-9-2017

 Global operation against illegal medicines

Global operation against illegal medicines

A global operation against illegal medicines has been completed. 123 countries participated, and the operation resulted in 354 arrests or further investigations and the suspension of more than 3,500 websites. Illegal sale of medicines is an increasing problem that may pose a global threat to public health. Sales often take place over the internet and across geographical borders. Consequently, the Danish Medicines Agency, the Danish Veterinary and Food Administration, the Danish Customs and Tax Administr...

Danish Medicines Agency

25-9-2017

Global operation against illegal medicines

Global operation against illegal medicines

A global operation against illegal medicines has been completed. 123 countries participated, and the operation resulted in 354 arrests or further investigations and the suspension of more than 3,500 websites.

Danish Medicines Agency

3-7-2017

 New fees for medicinal products, pharmaceutical companies and clinical trials from 1 July 2017

New fees for medicinal products, pharmaceutical companies and clinical trials from 1 July 2017

On 1 July 2017, a new executive order on fees payable for medicinal products, pharmaceutical companies and clinical trials became effective. The new fees involve changes in a number of areas. Changes in relation to marketing authorisations and variations etc. In connection with applications for marketing authorisations and variations etc., the new executive order entails a number of changes to the size of fees and the way in which they are calculated. Changes will be made to:Applications for new marketi...

Danish Medicines Agency

29-6-2017



DHPC – Cinryze 500 U (C1-INAKTIVATOR HUMAN)

DHPC – Cinryze 500 U (C1-INAKTIVATOR HUMAN)

Empfehlungen aufgrund eines möglichen Lieferengpasses

Swissmedic - Swiss Agency for Therapeutic Products

15-6-2017

Statement from FDA Commissioner Scott Gottlieb, M.D., on the 2016 National Youth Tobacco Survey results

Statement from FDA Commissioner Scott Gottlieb, M.D., on the 2016 National Youth Tobacco Survey results

While the latest numbers from the 2016 National Youth Tobacco Survey are encouraging, it is critical that we work to ensure this downward trend continues over the long term across all tobacco products. Every day in the U.S., more than 2,500 youth under the age of 18 smoke their first cigarette and more than 400 youth become daily cigarette smokers. It is also clear from these most recent numbers that youth are continuing to experiment with, or becoming regular users of, a wide range of other tobacco pro...

FDA - U.S. Food and Drug Administration

14-1-2017

Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk

Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk

Grange Co-op is initiating a recall of Rogue All Purpose Rabbit Pellets in 25# (25RP) 50# (50RP), 1,500# Tote (RP) no lot codes- purchased between March 1, 2016 and January 12, 2017 in Southern Oregon / Northern California from any Grange Co-op Retail Store or Wholesale Dealer. The recall is being initiated because samples tested by the Oregon Department of Agriculture discovered these products may contain higher than acceptable levels of vitamin D.

FDA - U.S. Food and Drug Administration

14-12-2017

ANTI-AGING FOUNDATION SPF 15 SHADE 500 (Octinoxate) Emulsion [La Prairie, Inc.]

ANTI-AGING FOUNDATION SPF 15 SHADE 500 (Octinoxate) Emulsion [La Prairie, Inc.]

Updated Date: Dec 14, 2017 EST

US - DailyMed

31-10-2017

Ultracet vs. Lortab

Ultracet vs. Lortab

Ultracet (tramadol and acetaminophen) and Lortab 5/500 (hydrocodone bitartrate and acetaminophen) are combination medications prescribed for the short-term relief of moderate to severe pain.

US - RxList

8-8-2017

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb)

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb)

Paracetamol / ibuprofen 500 mg / 150 mg Film-coated tablets (Paracomb) (Active substance: paracetamol / ibuprofen) - Community Referrals - Art 29 - Commission Decision (2017) 5646 of Tue, 08 Aug 2017 European Medicines Agency (EMA) procedure number: EMEA/H/A-29(4)/1447

Europe -DG Health and Food Safety

3-6-2017

More Than 500 Californians Given Life-Ending Drugs Since New Law Took Effect

More Than 500 Californians Given Life-Ending Drugs Since New Law Took Effect

Title: More Than 500 Californians Given Life-Ending Drugs Since New Law Took EffectCategory: Health NewsCreated: 6/1/2017 12:00:00 AMLast Editorial Review: 6/2/2017 12:00:00 AM

US - MedicineNet

30-5-2017

Triple Therapy More Cost-Effective Than MTX + Biologic in RA

Triple Therapy More Cost-Effective Than MTX + Biologic in RA

Patients with active rheumatoid arthritis (RA) did as well when switched from methotrexate (MTX) monotherapy to triple-drug therapy (MTX, sulfasalazine, and hydroxychloroquine) as when the biologic drug etanercept was added to ongoing MTX. Triple therapy saved more than $500,000 per patient for each year of good-quality life gained, the researchers found.

US - RxList

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