FEVORIT-CV 200 DT

Main information

Trade name:
FEVORIT-CV 200 DT 10

Available from:
Indoco Rem.

Composition:
10

Medicine domain:
Humans

Medicine type:
Allopathic drug

Documents

for the general public:
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for healthcare professionals:
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Localization

Available in:
India

Language:
English

Other information

Status

Source:
Central Drugs Standard Control Organization

Last update:
09-08-2016

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20-3-2018

Vietti Foods Issues Allergy Alert on Undeclared Wheat and Eggs in Southgate Hot Dog Chili Sauce

Vietti Foods is recalling approximately 200 cases of 15 oz cans of Southgate Hot Dog Chili Sauce, UPC 0 71846 95242 6, LOT # P642 M1217 70026. This recall has been initiated due to mislabeling because some of the cans may contain Dumplings with Chicken instead of Hot Dog Chili Sauce.

FDA - U.S. Food and Drug Administration

1-3-2018

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company is recalling approximately 200 cases of its Cherry SKI product because they are incorrectly labeled. Only the Cherry SKI products with the new design are being recalled, which were delivered to the southern Illinois, Evansville, IN and Winchester, OH markets.

FDA - U.S. Food and Drug Administration

5-10-2017

Surflink Media and Surflink Media 2 (Models 200 and 210) - used with wireless hearing aids

Recall for product correction - may cause interference with mobile towers

Therapeutic Goods Administration - Australia

20-9-2017

Nature Supplement Inc. Issues Voluntary Florida Recall of Vegetable Vigra Due to Undeclared Sildenafil

Natures Supplement, Inc. is voluntarily recalling 260 bottles of VEGETABLE VIGRA, 200 mg capsules to the consumer level. FDA analysis found this product to be tainted with Sidenafil. Sildenafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of Sildenafil in the Vegetable Vigra product renders it an unapproved drug for which safety and efficacy has not been established, therefore subject to recall.

FDA - U.S. Food and Drug Administration

10-9-2017

Bravo Produce Inc. Recalls Maradol Papaya from Productores Y Exportadores De Carica Papaya De Tecomán Y Costa Alegre SPR of RL and Packed by Frutas Selectas De Tijuana, S. De R.L. De C.V. Because of Possible Health Risk

Bravo Produce Inc. of San Ysidro, is withdrawing Maradol Papaya, grown by Productores y Exportadores de Carica Papaya de Tecomán y Costa Alegre SPR of RL and packed by Frutas Selectas de Tijuana, S. de RL de CV, as a preventive measure, because the product has tested positive for Salmonella by exams done by FDA. It is extremely important to mention that this bacterium can affect children, elderly and people with weak immune systems. Symptoms are fever, diarrhea, nausea, vomiting and abdominal pain.

FDA - U.S. Food and Drug Administration

22-8-2017

Chargenrückruf - Voriconazol Sandoz® 200mg, Filmtabletten

Swissmedic - Swiss Agency for Therapeutic Products

16-6-2017

Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut <sup>tm</sup> (Sodium Bicarbonate 4% Additive Solution), QUELICIN <sup>tm</sup> (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP

Hospira, Inc., a Pfizer company, is voluntarily recalling 42 lots of 8.4% Sodium Bicarbonate Injection, USP, 50 mL vials, 5 lots of NeutTM (Sodium Bicarbonate 4% additive solution) 5 mL vials, 5 lots of QUELICINTM (Succinylcholine Chloride Injection, USP) 200 mg/10 mL vials and 7 lots of Potassium Phosphates Injection, USP, 45 mM vials to the hospital/retail level due to microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of micr...

FDA - U.S. Food and Drug Administration

26-5-2017

Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle From That Lot

AstraZeneca today announced that the Company is notifying physicians and consumers that it is voluntarily recalling one lot of professional (physician) sample bottles containing eight tablets of BRILINTA (ticagrelor) 90mg tablets as a precautionary measure. This voluntary recall follows a report that a professional sample bottle containing eight tablets of BRILINTA 90mg also contained another medicine called ZURAMPIC (lesinurad) 200 mg tablets which is also manufactured by AstraZeneca.

FDA - U.S. Food and Drug Administration

17-4-2018

Company Recalls More Than 200 Million Eggs Due to Salmonella Scare

Title: Company Recalls More Than 200 Million Eggs Due to Salmonella ScareCategory: Health NewsCreated: 4/15/2018 12:00:00 AMLast Editorial Review: 4/16/2018 12:00:00 AM

US - MedicineNet

12-4-2018

VICKS VAPODROPS COUGH RELIEF (Menthol) Lozenge [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 12, 2018 EST

US - DailyMed

12-4-2018

VICKS VAPORUB CHILDRENS (Camphor (Synthetic), Eucalyptus Oil, And Menthol) Ointment [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 12, 2018 EST

US - DailyMed

12-4-2018

VICKS VAPOSTEAM (Camphor (Synthetic)) Liquid [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 12, 2018 EST

US - DailyMed

11-4-2018

PEPTO-BISMOL INSTACOOL (Bismuth Subsalicylate) Tablet, Chewable [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 11, 2018 EST

US - DailyMed

11-4-2018

VICKS VAPORUB (Camphor (Synthetic), Eucalyptus Oil, And Menthol) Ointment [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 11, 2018 EST

US - DailyMed

11-4-2018

CREST ANTI-CAVITY REGULAR (Sodium Fluoride) Paste, Dentifrice [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 11, 2018 EST

US - DailyMed

11-4-2018

PEPTO-BISMOL TO GO (Bismuth Subsalicylate) Tablet [Procter Gamble Manufactura S De RL De CV]

Updated Date: Apr 11, 2018 EST

US - DailyMed

12-3-2018

PEPTO KIDS (Calcium Carbonate) Tablet, Chewable [Procter Gamble Manufactura S De RL De CV]

Updated Date: Mar 12, 2018 EST

US - DailyMed

7-3-2018

VICKS VAPORUB LAVENDER SCENT (Camphor (Synthetic), Eucalyptus Oil, And Menthol) Ointment [Procter Gamble Manufactura S De RL De CV]

Updated Date: Mar 7, 2018 EST

US - DailyMed

7-3-2018

PEPTO-BISMOL (Bismuth Subsalicylate) Tablet [Procter Gamble Manufactura S De RL De CV]

Updated Date: Mar 7, 2018 EST

US - DailyMed

28-2-2018

HEMORRHOIDEX (Aesculus Hipp, Collinsonia, Hamamelis) Tablet [Nartex Laboratorios Homeopaticos SA DE CV]

Updated Date: Feb 28, 2018 EST

US - DailyMed

28-2-2018

ARNICA RECOVERY (Arnica Montana) Tablet [NARTEX LABORATORIOS HOMEOPATICOS SA DE CV]

Updated Date: Feb 28, 2018 EST

US - DailyMed

26-2-2018

EU/3/18/1984 (Omeros London Limited)

EU/3/18/1984 (Active substance: Recombinant human monoclonal antibody against mannan-binding lectin-associated serine protease-2) - Orphan designation - Commission Decision (2018)1251 of Mon, 26 Feb 2018 European Medicines Agency (EMA) procedure number: EMA/OD/200/17

Europe -DG Health and Food Safety

21-2-2018