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18-5-2018

7K and Poseidon 4500 by Shoreside Enterprises: Voluntary Recall - Due to Presence of Undeclared Sildenafil and/or Tadalafil

7K and Poseidon 4500 by Shoreside Enterprises: Voluntary Recall - Due to Presence of Undeclared Sildenafil and/or Tadalafil

Use of products with the undeclared active ingredients, sildenafil and tadalafil, may pose a threat to consumers because the active ingredient may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are the most at risk from these products. These products are considered ta...

FDA - U.S. Food and Drug Administration

17-5-2018

Shoreside Enterprises Issues Voluntary Nationwide Recall of 7K and Poseidon 4500 (Extreme 1000 Mg) Due to Presence of Undeclared Sildenafil and Tadalafil

Shoreside Enterprises Issues Voluntary Nationwide Recall of 7K and Poseidon 4500 (Extreme 1000 Mg) Due to Presence of Undeclared Sildenafil and Tadalafil

Shoreside Enterprises, Inc. is voluntarily recalling 7K (Lot specific: Lot #RO) and Poseidon 4500 (Extreme 1000 mg) (Lot specific: Lot #20117BL) to the consumer level. FDA analysis found the samples of these products to contain undeclared Sildenafil and/or Tadalafil. Sildenafil and Tadalafil are active ingredients in two FDA-approved prescription drugs used for the treatment of erectile dysfunction (ED).

FDA - U.S. Food and Drug Administration

17-4-2018

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

Overland Park, KS, Epic Products, LLC is voluntarily recalling all lots of Euphoric capsules, packaged in 1 count blister cards, 3 count bottles, and 12 count bottles to the consumer level. FDA analysis found samples of Euphoric to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterase 5-inhibitors (PDE-5 inhibitors), used to treat male erectile dysfunction (ED). The presence of sildenafil and tadalafil in E...

FDA - U.S. Food and Drug Administration

14-12-2017

Marmex Corp Issues Voluntary Nationwide Recall Of Blue Pearl All Natural Male Enhancement Supplement, Due To Undeclared Sildenafil

Marmex Corp Issues Voluntary Nationwide Recall Of Blue Pearl All Natural Male Enhancement Supplement, Due To Undeclared Sildenafil

Orange, CA, Marmex Corp is voluntarily recalling All lots of Blue Pearl All Natural Male Enhancement Supplement, 500mg to the consumer level. FDA analysis has found the products to contain sildenafil.

FDA - U.S. Food and Drug Administration

30-11-2017

Nutra Labs Inc. Issues Voluntary Nationwide Recall of Dietary Supplements Bull and Chao Jimengnan Tablets Due to Undeclared Active Pharmaceutical Ingredients

Nutra Labs Inc. Issues Voluntary Nationwide Recall of Dietary Supplements Bull and Chao Jimengnan Tablets Due to Undeclared Active Pharmaceutical Ingredients

Nutra Labs Inc. is voluntarily recalling lots sold by their firm of the male enhancement supplements Bull 1800 mg Capsules with the production date of 05/08/2016, and Chao Jimengnan 150 mg Tablets with Lot # 20151018 to the consumer level. FDA analysis found the products to be tainted with sildenafil, 0.026mg/capsule for Bull, and 70.46mg/tablet for Chao Jimengnan respectively. Sildenafil is the active pharmaceutical ingredient in an FDA approved product used for erectile dysfunction, making Bull capsule...

FDA - U.S. Food and Drug Administration

5-10-2017

Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7 Platinum 5000, Papa Zen 3300, Fifty Shades 6000 and Grande X 5800, Due to Presence of Undeclared Sildenafil, Tadalafil and Desmethyl Carbodenafil

Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7 Platinum 5000, Papa Zen 3300, Fifty Shades 6000 and Grande X 5800, Due to Presence of Undeclared Sildenafil, Tadalafil and Desmethyl Carbodenafil

Newark, CA, Gadget Island, Inc. is voluntarily recalling Rhino 7 Platinum 5000 capsules, All LOTS, Papa Zen 3300 capsules, LOT# NSS050888, Fifty Shades 6000 capsules, all Lots, Grande X 5800 capsules, all Lots, to the consumer level. FDA analysis has found the products to be tainted with Sildenafil and Tadalafil, which are the active ingredients in two FDA-approved prescription drugs used for the treatment of erectile dysfunction (ED), as well as Desmethyl Carbodenafil which is structurally similar to si...

FDA - U.S. Food and Drug Administration

20-9-2017

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

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

21-7-2017

Ultra Shop Supplement Issues Voluntary Nationwide Recall of Super Panther 7K Due to Presence of Undeclared Sildenafil and Tadalafil

Ultra Shop Supplement Issues Voluntary Nationwide Recall of Super Panther 7K Due to Presence of Undeclared Sildenafil and Tadalafil

Charlotte, NC, Ultra Shop Supplement is voluntarily recalling Super Panther 7K capsules, [1 count blister card Lot#: RO846356 and 6 count bottle Lot RO246852 within expiry], distributed by SX Power Co., Brooklyn, NY, to the consumer level. FDA analysis found samples of Super Panther 7K to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterate 5-inhibitors (PDE-5), used to treat erectile dysfunction (ED).

FDA - U.S. Food and Drug Administration

16-4-2018

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [REMEDYREPACK INC.]

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [REMEDYREPACK INC.]

Updated Date: Apr 16, 2018 EST

US - DailyMed

23-2-2018

SILDENAFIL CITRATE Tablet [Major Pharmaceuticals]

SILDENAFIL CITRATE Tablet [Major Pharmaceuticals]

Updated Date: Feb 23, 2018 EST

US - DailyMed

6-2-2018

SILDENAFIL CITRATE Powder [H3 MEDICAL INC.]

SILDENAFIL CITRATE Powder [H3 MEDICAL INC.]

Updated Date: Feb 6, 2018 EST

US - DailyMed

24-1-2018

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [PD-Rx Pharmaceuticals, Inc.]

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [PD-Rx Pharmaceuticals, Inc.]

Updated Date: Jan 24, 2018 EST

US - DailyMed

16-1-2018

SILDENAFIL CITRATE (Sildenafil) Tablet, Film Coated [Vensun Pharmaceuticals, Inc. ]

SILDENAFIL CITRATE (Sildenafil) Tablet, Film Coated [Vensun Pharmaceuticals, Inc. ]

Updated Date: Jan 16, 2018 EST

US - DailyMed

16-1-2018

AX PHARMACEUTICAL CORP (Sildenafil Citrate) Powder [AX Pharmaceutical Corp]

AX PHARMACEUTICAL CORP (Sildenafil Citrate) Powder [AX Pharmaceutical Corp]

Updated Date: Jan 16, 2018 EST

US - DailyMed

26-12-2017

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Bryant Ranch Prepack]

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Bryant Ranch Prepack]

Updated Date: Dec 26, 2017 EST

US - DailyMed

21-12-2017

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Cardinal Health]

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Cardinal Health]

Updated Date: Dec 21, 2017 EST

US - DailyMed

1-12-2017

SILDENAFIL CITRATE Tablet, Film Coated [Greenstone LLC]

SILDENAFIL CITRATE Tablet, Film Coated [Greenstone LLC]

Updated Date: Dec 1, 2017 EST

US - DailyMed

7-11-2017

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Pfizer Laboratories Div Pfizer Inc]

VIAGRA (Sildenafil Citrate) Tablet, Film Coated [Pfizer Laboratories Div Pfizer Inc]

Updated Date: Nov 7, 2017 EST

US - DailyMed

7-11-2017

SILDENAFIL (Sildenafil Citrate) Tablet, Film Coated [Greenstone LLC]

SILDENAFIL (Sildenafil Citrate) Tablet, Film Coated [Greenstone LLC]

Updated Date: Nov 7, 2017 EST

US - DailyMed

18-10-2017

SILDENAFIL (Sildenafil Citrate) Tablet, Film Coated [PD-Rx Pharmaceuticals, Inc.]

SILDENAFIL (Sildenafil Citrate) Tablet, Film Coated [PD-Rx Pharmaceuticals, Inc.]

Updated Date: Oct 18, 2017 EST

US - DailyMed

19-9-2017

SILDENAFIL CITRATE Tablet [Torrent Pharmaceuticals Limited]

SILDENAFIL CITRATE Tablet [Torrent Pharmaceuticals Limited]

Updated Date: Sep 19, 2017 EST

US - DailyMed

21-8-2017

AX (Sildenafil Citrate) Powder [AX Pharmaceutical Corp]

AX (Sildenafil Citrate) Powder [AX Pharmaceutical Corp]

Updated Date: Aug 21, 2017 EST

US - DailyMed

6-6-2017

SILDENAFIL (Sildenafil Citrate) Injection, Solution [AuroMedics Pharma LLC]

SILDENAFIL (Sildenafil Citrate) Injection, Solution [AuroMedics Pharma LLC]

Updated Date: Jun 6, 2017 EST

US - DailyMed