Carl and update with natural methods
My husband in case you are new or to refresh your memory was diagnosed with colorectal cancer 9 weeks ago. Went in for his coloscopy and sent immediately for surgery. Had a couple bouts of back in the hospital after the initial release.
So far he is doing great. We have chosen at this time to go as natural as possible. They got the tumor but the local facility still want to do 6 months of chemo sandwhiched on top of 6-8 weeks of chemo/rads. Other dr.s from back east and other larger towns in our area after looking at his files have all said at most the chemo/rads is all he needs.
After much research and keeping in mind that chemo/rads may be needed at a later date we have definitely chosen to not use them at this time. He is currently doing Bloodroot, Montana Yewtip and Maitake mushrooms. Next week he begins a bundle that has all these and more. We had purchased all this prior to finding a guy in a near by town that puts together bundles specific to his cancer. His energy levels have only been increasing. Oh and he is taking Vitamin D3 and melatonin at night which not only are helping him sleep but his night sweats have stopped and we recently learned there is some connections of melatonin helping cancer.
So I will try and remember to come back with updates and how things are going and results as we go along.
Comments
-
I sure hope there's blind
I sure hope there's blind studies, etc., on this natural path your heading down.
It's a life at stake.0 -
There's no "blind studies" with alternativesherdizziness said:I sure hope there's blind
I sure hope there's blind studies, etc., on this natural path your heading down.
It's a life at stake.
With TCM, there's over 3,000 years of life.
"Blind studies" has brought you:
----------
1. Vioxx - I'm sure you're familiar with this infamous anti-inflammatory. Merck had to pull Vioxx off the global market in 2004 after a clinical study demonstrated that it significantly increased the risk of cardiovascular "events" such as heart attacks and strokes.
2. Bextra - Like Vioxx, this prescription painkiller caused an increased risk of heart attack and stroke. Pfizer pulled it off the market in the U.S. a year after the Vioxx fiasco in 2005.
3. Cylert - Abbott pulled the Attention Deficit Hyperactivity Disorder (ADHD) drug off the U.S. market in 2005 after the FDA discovered 13 cases of liver failure. Turns out that Cylert patients have as much as a 25 percent higher rate of liver failure compared to the general population.
4. Baycol - This cholesterol-lowering drug caused users to suffer from a much higher rate of rhabdomyolysis, a debilitating muscle ailment that can be fatal. There were 31 reported deaths that were directly linked to Baycol, and it was yanked off the market in the U.S. in 2001.
5. Palladone - This slow-release narcotic painkiller by Purdue Pharma was pulled off the market in the U.S. in 2005 because it was found to cause side effects like depression and even coma when mixed with alcohol.
----------
And:
US Recall News
Tuesday, July 27, 2010
Drug Recalls and recalled medical devices from pharmaceutical industry and Food and Drug Administration (FDA) press releases.
Cook Recalls Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays
July 22, 2010
Cook has initiated a voluntary recall of certain lots of its Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that contain a Covidien 6PERC or 8PERC Shiley™ Tracheostomy Tube.
Written by: FDA · Filed Under FDA Press Releases
Good Health, Inc. Recalls Vialipro – Contains Prescription-Only Ingredients
July 21, 2010
Good Health, Inc. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement Vialipro for sexual enhancement sold under the Lot Numbers listed below.
Written by: FDA · Filed Under FDA Press Releases
Bristol-Myers Squibb Recalls Coumadin (R) 1 mg Tablet Blister Packs
July 15, 2010
Bristol-Myers Squibb is recalling three lots of physician sample blister packs of Coumadin® 1 mg tablets and five lots, of Coumadin 1 mg tablet hospital unit dose (HUD) blister packs.
Written by: FDA · Filed Under Drug Recalls
INZ Distributors Inc. / Magic Power Coffee Inc. Recalls Magic Power Coffee Dietary Supplement
June 29, 2010
INZ DISTRIBUTORS INC./MAGIC POWER COFFEE INC. of Brooklyn, NY announced today that it is conducting a voluntary nationwide recall of the dietary supplement product sold under the name, Magic Power Coffee.
Written by: FDA · Filed Under FDA Press Releases
Scope Original Mint Mouthwash Recalled by P&G: Failure to Meet Child-Resistant Closure Requirement
June 26, 2010
WASHINGTON, D.C. – THE U.S. CONSUMER PRODUCT SAFETY COMMISSION, IN COOPERATION WITH THE FIRM NAMED BELOW, TODAY ANNOUNCED A VOLUNTARY RECALL OF THE FOLLOWING CONSUMER PRODUCT. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED. IT IS ILLEGAL TO RESELL OR ATTEMPT TO RESELL A RECALLED CONSUMER PRODUCT.
Written by: CPSC · Filed Under Drug Recalls
P&G Recalls 4 Hour Decongestant Nasal Spray
June 26, 2010
The Procter & Gamble Company (P&G) announced is voluntarily recalling its 4-Hour Decongestant Nasal Spray. The product was distributed nationwide in the United States.
The company said it is taking this voluntary precautionary step after finding that the product formulation may not meet the expiration dates on the package. This recall is not a result of consumer complaints.
Written by: FDA · Filed Under FDA Press Releases
Mcneil Recalls Benadryl and Tylenol
June 18, 2010
FOR IMMEDIATE RELEASEMcNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH TYLENOL® Rapid Release Gels, 50 count sold in the U.S., Trinidad and Tobago, Bermuda, and Puerto Rico (FULL RECALLED PRODUCT LIST BELOW). This recall is a follow-up to the product recall that McNeil Consumer Healthcare announced on January 15th, 2010 and is being taken because the products were inadvertently omitted from the initial recall action. McNeil Consumer Healthcare identified the omission and informed the U.S. Food and Drug Administration (FDA) of its decision to add these product lots to the recall list. All these products were produced before the January 15th, 2010 recall. Since January, McNeil Consumer Healthcare has continued to analyze and evaluate 2,4,6-tribromoanisole (TBA) and has shared that information with the FDA. This further analysis confirms that the risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the FDA.
Written by: FDA · Filed Under FDA Press Releases
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags
June 9, 2010
West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.
Written by: FDA · Filed Under FDA Press Releases
Pfizer Recalls Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
June 9, 2010
Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery. These products are supplied in plastic IV bags.
Written by: FDA · Filed Under FDA Press Releases
Sagent Pharmaceuticals Recalls All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
June 8, 2010
Sagent Pharmaceuticals, Inc. announced the voluntary nationwide recall of all lots of ondansetron injection in 5% dextrose 32mg / 50 mL (NDC number 25021-776-50) manufactured by Claris Lifesciences and distributed by Sagent. The lot numbers being recalled are: A090309, A090310, A090311 and A090312, which were distributed to hospitals, wholesalers and distributors nationwide from August 2009 through May 2010. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery and is supplied in a single dose plastic container.
Written by: FDA · Filed Under FDA Press Releases
Claris Lifesciences Recalls Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.
June 3, 2010
Claris Lifesciences today announces the voluntary nationwide recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL (NDC 36000-008-24), Ciprofloxacin Inj. USP 400 mg / 200 mL (NDC 36000-009-24), Metronidazole Inj. USP 500 mg/100 ml (NDC 36000-001-24), and Ondansetron in 5% Dextrose Inj. 32 mg / 50 mL (36000-014-06) manufactured and distributed by Claris Lifesciences. All lots are being recalled, which were distributed to hospitals, wholesalers and distributors nationwide.
Written by: FDA · Filed Under FDA Press Releases
Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children’s Products
May 29, 2010
Blacksmith Brands, Inc., in consultation with the U.S. Food and Drug Administration, is voluntarily recalling all lots of four children’s products in the PediaCare line. These products are sold exclusively in the United States. These products were manufactured for Blacksmith Brands by McNeil Consumer Healthcare, a Division of McNeil-PPC, Inc., (a Johnson & Johnson Company) at McNeil’s Fort Washington, PA plant.
Written by: FDA · Filed Under FDA Press Releases
Hospira Announces Expands Recall of Certain Lots of Liposyn and Propofol That May Contain Particulate Matter
May 29, 2010
Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, announced today it is voluntarily expanding its March 31, 2010, recall of Propofol Injectable Emulsion 1% and Liposyn™ (Intravenous Fat Emulsion) products which include Liposyn II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, and Liposyn III 30% to the consumer or user level. Hospira is conducting the recall because some of the containers may contain particulate matter. The particulate is primarily made up of sub-visible inert stainless steel particles.
Written by: FDA · Filed Under FDA Press Releases
Equate Ibuprofen Recall – 200mg Tablets – Metal Shavings in Bottles
May 27, 2010
L. Perrigo Co has recalled one lot of Equate Ibuprofen 200 mg tablets packaged in bottles of 100 tablets. These recalled Equate Ibuprofen tablets have lot number 9BE1961 printed on the label or stamped on the bottle. The pills are being recalled because there may be metal shavings in the containers.
Written by: E. Sizemore · Filed Under Drug Recalls
Recall of HYLENEX Recombinant Initiated by Baxter
May 22, 2010
Baxter International Inc. (NYSE:BAX) announced today that a voluntary recall of all manufactured lots of HYLENEX recombinant (hyaluronidase human injection) has been initiated as a precautionary measure due to instances of particulate matter observed in a limited number of HYLENEX vials during routine stability testing. Baxter is working with the product’s NDA-holder, Halozyme Therapeutics, to investigate the root cause of the issue and appropriately address the situation.
Written by: FDA · Filed Under FDA Press Releases
Rise ‘N Roll Bakery Issues Allergy Alert on Undeclared Milk in ‘Gourmet Cookie Mixes’
May 21, 2010
RECALLS, MARKET WITHDRAWALS, & SAFETY ALERTS ARCHIVE FOR RECALLS, MARKET WITHDRAWALS & SAFETY ALERTS ENFORCEMENT REPORTS INDUSTRY GUIDANCE MAJOR PRODUCT RECALLS VAR CID_ID, CID_ITEM, CID_CLASS, CONTENT_PAGE = 0; VAR BREAKOUT = FALSE; VAR CID = WINDOW.LOCATION.HREF.SPLIT(“/”); VAR CID_FILENAME = CID; IF(CID_FILENAME.TOLOWERCASE() == “DEFAULT.HTM” || CID_FILENAME.TOLOWERCASE() == “INDEX.HTM” ) { CID_ID = DOCUMENT.GETELEMENTBYID(“LEFT_NAV_2202″); IF(CID_ID.CLASSNAME == “SIDEMENU_PARENT”) { BREAKOUT = TRUE; } } ELSE { CID_ITEM = CID_FILENAME.SPLIT(“.”); CID_ID = DOCUMENT.GETELEMENTBYID(CID_ITEM.TOUPPERCASE()); CONTENT_PAGE = 1; } IF(BREAKOUT == FALSE) { IF (CID_ID && CONTENT_PAGE == 1) { VAR CID_IMG_TEXT=” “; VAR CID_ID_INNERTEXT = CID_ID.INNERHTML; CID_IMG_TEXT += CID_ID_INNERTEXT; CID_ID.INNERHTML = CID_IMG_TEXT+”"; } ELSE IF(CID_ID) { VAR CID_IMG_TEXT=”“; VAR CID_ID_INNERTEXT = CID_ID.INNERHTML; IF((CID_ID_INNERTEXT.TOLOWERCASE()).INDEXOF(“”) >= 0) { VAR INDEXER = (CID_ID_INNERTEXT.TOLOWERCASE()).INDEXOF(“”); VAR BEG = CID_ID_INNERTEXT.SUBSTRING(0, INDEXER); VAR END = CID_ID_INNERTEXT.SUBSTRING(INDEXER); CID_ID.INNERHTML = CID_IMG_TEXT + BEG + “” + END; } ELSE { CID_IMG_TEXT += CID_ID_INNERTEXT; CID_ID.INNERHTML = CID_IMG_TEXT+”"; } } } RECALL — FIRM PRESS RELEASE
Written by: FDA · Filed Under FDA Press Releases
Copyright © 2007 US Recall News · WP theme by Brian Gardner · Website by Everett Sizemore · Our Attorney Network
Important Disclaimer: US Recall News suggests that consumers should ALWAYS contact the governing agency for more information about product recalls. US Recall News is NOT a government agency. We are not attorneys, and we are not medical professionals. This is a privately-run website and its purpose is to provide a portal for information about product recalls. This information is NOT complete or all-inclusive and you should NOT rely on US Recall News as your only source for product recall updates. We suggest you pay attention to manufacturer and product distributor websites and press releases, as well as the websites and press releases from the FDA, USDA, CPSC, EPA, NHTSA and US Coast Guard.
------------------
It should be noted, that alternative medicine is rarely "recalled".
There -are- other, safe ways to fight cancer!
John0 -
Natural medicine isn't regulatedJohn23 said:There's no "blind studies" with alternatives
With TCM, there's over 3,000 years of life.
"Blind studies" has brought you:
----------
1. Vioxx - I'm sure you're familiar with this infamous anti-inflammatory. Merck had to pull Vioxx off the global market in 2004 after a clinical study demonstrated that it significantly increased the risk of cardiovascular "events" such as heart attacks and strokes.
2. Bextra - Like Vioxx, this prescription painkiller caused an increased risk of heart attack and stroke. Pfizer pulled it off the market in the U.S. a year after the Vioxx fiasco in 2005.
3. Cylert - Abbott pulled the Attention Deficit Hyperactivity Disorder (ADHD) drug off the U.S. market in 2005 after the FDA discovered 13 cases of liver failure. Turns out that Cylert patients have as much as a 25 percent higher rate of liver failure compared to the general population.
4. Baycol - This cholesterol-lowering drug caused users to suffer from a much higher rate of rhabdomyolysis, a debilitating muscle ailment that can be fatal. There were 31 reported deaths that were directly linked to Baycol, and it was yanked off the market in the U.S. in 2001.
5. Palladone - This slow-release narcotic painkiller by Purdue Pharma was pulled off the market in the U.S. in 2005 because it was found to cause side effects like depression and even coma when mixed with alcohol.
----------
And:
US Recall News
Tuesday, July 27, 2010
Drug Recalls and recalled medical devices from pharmaceutical industry and Food and Drug Administration (FDA) press releases.
Cook Recalls Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays
July 22, 2010
Cook has initiated a voluntary recall of certain lots of its Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that contain a Covidien 6PERC or 8PERC Shiley™ Tracheostomy Tube.
Written by: FDA · Filed Under FDA Press Releases
Good Health, Inc. Recalls Vialipro – Contains Prescription-Only Ingredients
July 21, 2010
Good Health, Inc. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement Vialipro for sexual enhancement sold under the Lot Numbers listed below.
Written by: FDA · Filed Under FDA Press Releases
Bristol-Myers Squibb Recalls Coumadin (R) 1 mg Tablet Blister Packs
July 15, 2010
Bristol-Myers Squibb is recalling three lots of physician sample blister packs of Coumadin® 1 mg tablets and five lots, of Coumadin 1 mg tablet hospital unit dose (HUD) blister packs.
Written by: FDA · Filed Under Drug Recalls
INZ Distributors Inc. / Magic Power Coffee Inc. Recalls Magic Power Coffee Dietary Supplement
June 29, 2010
INZ DISTRIBUTORS INC./MAGIC POWER COFFEE INC. of Brooklyn, NY announced today that it is conducting a voluntary nationwide recall of the dietary supplement product sold under the name, Magic Power Coffee.
Written by: FDA · Filed Under FDA Press Releases
Scope Original Mint Mouthwash Recalled by P&G: Failure to Meet Child-Resistant Closure Requirement
June 26, 2010
WASHINGTON, D.C. – THE U.S. CONSUMER PRODUCT SAFETY COMMISSION, IN COOPERATION WITH THE FIRM NAMED BELOW, TODAY ANNOUNCED A VOLUNTARY RECALL OF THE FOLLOWING CONSUMER PRODUCT. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED. IT IS ILLEGAL TO RESELL OR ATTEMPT TO RESELL A RECALLED CONSUMER PRODUCT.
Written by: CPSC · Filed Under Drug Recalls
P&G Recalls 4 Hour Decongestant Nasal Spray
June 26, 2010
The Procter & Gamble Company (P&G) announced is voluntarily recalling its 4-Hour Decongestant Nasal Spray. The product was distributed nationwide in the United States.
The company said it is taking this voluntary precautionary step after finding that the product formulation may not meet the expiration dates on the package. This recall is not a result of consumer complaints.
Written by: FDA · Filed Under FDA Press Releases
Mcneil Recalls Benadryl and Tylenol
June 18, 2010
FOR IMMEDIATE RELEASEMcNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH TYLENOL® Rapid Release Gels, 50 count sold in the U.S., Trinidad and Tobago, Bermuda, and Puerto Rico (FULL RECALLED PRODUCT LIST BELOW). This recall is a follow-up to the product recall that McNeil Consumer Healthcare announced on January 15th, 2010 and is being taken because the products were inadvertently omitted from the initial recall action. McNeil Consumer Healthcare identified the omission and informed the U.S. Food and Drug Administration (FDA) of its decision to add these product lots to the recall list. All these products were produced before the January 15th, 2010 recall. Since January, McNeil Consumer Healthcare has continued to analyze and evaluate 2,4,6-tribromoanisole (TBA) and has shared that information with the FDA. This further analysis confirms that the risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the FDA.
Written by: FDA · Filed Under FDA Press Releases
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags
June 9, 2010
West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.
Written by: FDA · Filed Under FDA Press Releases
Pfizer Recalls Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
June 9, 2010
Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery. These products are supplied in plastic IV bags.
Written by: FDA · Filed Under FDA Press Releases
Sagent Pharmaceuticals Recalls All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
June 8, 2010
Sagent Pharmaceuticals, Inc. announced the voluntary nationwide recall of all lots of ondansetron injection in 5% dextrose 32mg / 50 mL (NDC number 25021-776-50) manufactured by Claris Lifesciences and distributed by Sagent. The lot numbers being recalled are: A090309, A090310, A090311 and A090312, which were distributed to hospitals, wholesalers and distributors nationwide from August 2009 through May 2010. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery and is supplied in a single dose plastic container.
Written by: FDA · Filed Under FDA Press Releases
Claris Lifesciences Recalls Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.
June 3, 2010
Claris Lifesciences today announces the voluntary nationwide recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL (NDC 36000-008-24), Ciprofloxacin Inj. USP 400 mg / 200 mL (NDC 36000-009-24), Metronidazole Inj. USP 500 mg/100 ml (NDC 36000-001-24), and Ondansetron in 5% Dextrose Inj. 32 mg / 50 mL (36000-014-06) manufactured and distributed by Claris Lifesciences. All lots are being recalled, which were distributed to hospitals, wholesalers and distributors nationwide.
Written by: FDA · Filed Under FDA Press Releases
Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children’s Products
May 29, 2010
Blacksmith Brands, Inc., in consultation with the U.S. Food and Drug Administration, is voluntarily recalling all lots of four children’s products in the PediaCare line. These products are sold exclusively in the United States. These products were manufactured for Blacksmith Brands by McNeil Consumer Healthcare, a Division of McNeil-PPC, Inc., (a Johnson & Johnson Company) at McNeil’s Fort Washington, PA plant.
Written by: FDA · Filed Under FDA Press Releases
Hospira Announces Expands Recall of Certain Lots of Liposyn and Propofol That May Contain Particulate Matter
May 29, 2010
Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, announced today it is voluntarily expanding its March 31, 2010, recall of Propofol Injectable Emulsion 1% and Liposyn™ (Intravenous Fat Emulsion) products which include Liposyn II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, and Liposyn III 30% to the consumer or user level. Hospira is conducting the recall because some of the containers may contain particulate matter. The particulate is primarily made up of sub-visible inert stainless steel particles.
Written by: FDA · Filed Under FDA Press Releases
Equate Ibuprofen Recall – 200mg Tablets – Metal Shavings in Bottles
May 27, 2010
L. Perrigo Co has recalled one lot of Equate Ibuprofen 200 mg tablets packaged in bottles of 100 tablets. These recalled Equate Ibuprofen tablets have lot number 9BE1961 printed on the label or stamped on the bottle. The pills are being recalled because there may be metal shavings in the containers.
Written by: E. Sizemore · Filed Under Drug Recalls
Recall of HYLENEX Recombinant Initiated by Baxter
May 22, 2010
Baxter International Inc. (NYSE:BAX) announced today that a voluntary recall of all manufactured lots of HYLENEX recombinant (hyaluronidase human injection) has been initiated as a precautionary measure due to instances of particulate matter observed in a limited number of HYLENEX vials during routine stability testing. Baxter is working with the product’s NDA-holder, Halozyme Therapeutics, to investigate the root cause of the issue and appropriately address the situation.
Written by: FDA · Filed Under FDA Press Releases
Rise ‘N Roll Bakery Issues Allergy Alert on Undeclared Milk in ‘Gourmet Cookie Mixes’
May 21, 2010
RECALLS, MARKET WITHDRAWALS, & SAFETY ALERTS ARCHIVE FOR RECALLS, MARKET WITHDRAWALS & SAFETY ALERTS ENFORCEMENT REPORTS INDUSTRY GUIDANCE MAJOR PRODUCT RECALLS VAR CID_ID, CID_ITEM, CID_CLASS, CONTENT_PAGE = 0; VAR BREAKOUT = FALSE; VAR CID = WINDOW.LOCATION.HREF.SPLIT(“/”); VAR CID_FILENAME = CID; IF(CID_FILENAME.TOLOWERCASE() == “DEFAULT.HTM” || CID_FILENAME.TOLOWERCASE() == “INDEX.HTM” ) { CID_ID = DOCUMENT.GETELEMENTBYID(“LEFT_NAV_2202″); IF(CID_ID.CLASSNAME == “SIDEMENU_PARENT”) { BREAKOUT = TRUE; } } ELSE { CID_ITEM = CID_FILENAME.SPLIT(“.”); CID_ID = DOCUMENT.GETELEMENTBYID(CID_ITEM.TOUPPERCASE()); CONTENT_PAGE = 1; } IF(BREAKOUT == FALSE) { IF (CID_ID && CONTENT_PAGE == 1) { VAR CID_IMG_TEXT=” “; VAR CID_ID_INNERTEXT = CID_ID.INNERHTML; CID_IMG_TEXT += CID_ID_INNERTEXT; CID_ID.INNERHTML = CID_IMG_TEXT+”"; } ELSE IF(CID_ID) { VAR CID_IMG_TEXT=”“; VAR CID_ID_INNERTEXT = CID_ID.INNERHTML; IF((CID_ID_INNERTEXT.TOLOWERCASE()).INDEXOF(“”) >= 0) { VAR INDEXER = (CID_ID_INNERTEXT.TOLOWERCASE()).INDEXOF(“”); VAR BEG = CID_ID_INNERTEXT.SUBSTRING(0, INDEXER); VAR END = CID_ID_INNERTEXT.SUBSTRING(INDEXER); CID_ID.INNERHTML = CID_IMG_TEXT + BEG + “” + END; } ELSE { CID_IMG_TEXT += CID_ID_INNERTEXT; CID_ID.INNERHTML = CID_IMG_TEXT+”"; } } } RECALL — FIRM PRESS RELEASE
Written by: FDA · Filed Under FDA Press Releases
Copyright © 2007 US Recall News · WP theme by Brian Gardner · Website by Everett Sizemore · Our Attorney Network
Important Disclaimer: US Recall News suggests that consumers should ALWAYS contact the governing agency for more information about product recalls. US Recall News is NOT a government agency. We are not attorneys, and we are not medical professionals. This is a privately-run website and its purpose is to provide a portal for information about product recalls. This information is NOT complete or all-inclusive and you should NOT rely on US Recall News as your only source for product recall updates. We suggest you pay attention to manufacturer and product distributor websites and press releases, as well as the websites and press releases from the FDA, USDA, CPSC, EPA, NHTSA and US Coast Guard.
------------------
It should be noted, that alternative medicine is rarely "recalled".
There -are- other, safe ways to fight cancer!
John
Per John: "It should be noted, that alternative medicine is rarely "recalled".
Doesn't mean natural medicine is safe. Just it doesn't fall under federal regulations.
My Grandmother was a full Alaskan Native, in my family my great, great grandmother was a shaman. No one followed in her footsteps. Not to say her way was wrong, just that western medicine came along. My family uses western medicine, when it comes to heart attacks, strokes and cancer. We use native medicine for arthritis, Grandma didn't raise dummies.0 -
Oh-ooh...?herdizziness said:Natural medicine isn't regulated
Per John: "It should be noted, that alternative medicine is rarely "recalled".
Doesn't mean natural medicine is safe. Just it doesn't fall under federal regulations.
My Grandmother was a full Alaskan Native, in my family my great, great grandmother was a shaman. No one followed in her footsteps. Not to say her way was wrong, just that western medicine came along. My family uses western medicine, when it comes to heart attacks, strokes and cancer. We use native medicine for arthritis, Grandma didn't raise dummies.
Re:
"My family uses western medicine, when it comes to heart attacks,
strokes and cancer. We use native medicine for arthritis, Grandma
didn't raise dummies."
I was taught at a very early age, never to discount anything without
first learning all I can about it. Doing otherwise is not only foolish
prejudice, but it removes the ability to learn about things that can be
of great benefit.
We didn't have too many dummies in our family either.
Stay well; think healthy.
John0 -
And there againJohn23 said:Oh-ooh...?
Re:
"My family uses western medicine, when it comes to heart attacks,
strokes and cancer. We use native medicine for arthritis, Grandma
didn't raise dummies."
I was taught at a very early age, never to discount anything without
first learning all I can about it. Doing otherwise is not only foolish
prejudice, but it removes the ability to learn about things that can be
of great benefit.
We didn't have too many dummies in our family either.
Stay well; think healthy.
John
Aggressive stage 3 into 6 lymph nodes ,48 sessions of 5Fu, 216 tablets of levamisole 12 years 8mos ca free,crap health ,but ca free. Whatever gets you thru the night. Ron.0 -
Ron -ron50 said:And there again
Aggressive stage 3 into 6 lymph nodes ,48 sessions of 5Fu, 216 tablets of levamisole 12 years 8mos ca free,crap health ,but ca free. Whatever gets you thru the night. Ron.
Re:
"Whatever gets you thru the night."
Ditto!
If chemo and radiation does the trick, then it's a good deal!
There's nothing wrong with doing -whatever- it takes to get rid
of the rogue cells.
But if one sees that the methods and treatments they are getting
aren't working, or causing other bad things, then they shouldn't be
afraid to try something totally different. And I'm saying that, not
just for those taking western medicine, but for anyone using any
method or procedure; TCM, juicing, etc., included.
Chemo, toxic chemicals, and radiation aren't the only things that
are able to kill cancer cells and tumors. There are many alternatives
that have great merit, and do very well for those that have gone
that route.
Likewise, most of the alternatives do not work fast enough to
remedy a tumor that's about to kill the patient within a short amount
of time (weeks, days), so western medicine would be a better choice.
The point is, as you said so well: "Whatever gets you thru the night."
Being afraid of cancer killing us, isn't a good reason to avoid
what can save us. There are other options available, and to
discount them is downright foolish.
There are a whole lot of us out here that have opted to do other
than the mainstream medicine that's pushed daily by the industry.
One of these days, we should have a "show of hands". Perhaps
that will give some people the courage to fight for survival regardless
of the failure that they might be having with the industry's approach.
I am truly happy for all those that are alive thanks to modern medicine,
but terribly saddened by all those that I read about daily, that are dying
due to the failures of the same modern medicine.
There isn't "just one way" to fight this damned thing, and those that
encourage and perpetuate the Fear of trying something different, are
just causing the perpetuation of deaths from this malady.
Fear is never a good excuse to remain in front of a moving train,
instead of jumping off the trestle.
Stay well !!
John0 -
Has to be your choice:)ron50 said:And there again
Aggressive stage 3 into 6 lymph nodes ,48 sessions of 5Fu, 216 tablets of levamisole 12 years 8mos ca free,crap health ,but ca free. Whatever gets you thru the night. Ron.
Ron I agree whatever gets one thru the night.
We did lots of weighing of our situation, homework on options we are trying, working closely with our naturopath and a local herbalist for bundles. Carls stats Stage 2, N0, M0 26 nodes all negative. The whole tumor was removed and contained w/in the colon area...was just starting to go thru the rectal wall. We know the risks of each option. For now he will do his colonoscopies, bloodwork etc but for now feels he has to try this route first if it doesn't work he will look at other routes. After 10 yrs as a wrecker driver and not being with his family if all he had left was a couple of years he doesn't want to spend it sicker than a dog the way chemo/rads will make him. He feels this is something he has to try and has it in the back of his mind that the other route may be necessary.0 -
Carl-Renee:Carl_Renee said:Has to be your choice:)
Ron I agree whatever gets one thru the night.
We did lots of weighing of our situation, homework on options we are trying, working closely with our naturopath and a local herbalist for bundles. Carls stats Stage 2, N0, M0 26 nodes all negative. The whole tumor was removed and contained w/in the colon area...was just starting to go thru the rectal wall. We know the risks of each option. For now he will do his colonoscopies, bloodwork etc but for now feels he has to try this route first if it doesn't work he will look at other routes. After 10 yrs as a wrecker driver and not being with his family if all he had left was a couple of years he doesn't want to spend it sicker than a dog the way chemo/rads will make him. He feels this is something he has to try and has it in the back of his mind that the other route may be necessary.
With your cancer being a Stage II, there are people,Stage II, that chose not to do chemo or to whom chemo is not offered, depending upon the patient.
Best wishes with the route you have chosen to take.
Tina.0 -
FearJohn23 said:Ron -
Re:
"Whatever gets you thru the night."
Ditto!
If chemo and radiation does the trick, then it's a good deal!
There's nothing wrong with doing -whatever- it takes to get rid
of the rogue cells.
But if one sees that the methods and treatments they are getting
aren't working, or causing other bad things, then they shouldn't be
afraid to try something totally different. And I'm saying that, not
just for those taking western medicine, but for anyone using any
method or procedure; TCM, juicing, etc., included.
Chemo, toxic chemicals, and radiation aren't the only things that
are able to kill cancer cells and tumors. There are many alternatives
that have great merit, and do very well for those that have gone
that route.
Likewise, most of the alternatives do not work fast enough to
remedy a tumor that's about to kill the patient within a short amount
of time (weeks, days), so western medicine would be a better choice.
The point is, as you said so well: "Whatever gets you thru the night."
Being afraid of cancer killing us, isn't a good reason to avoid
what can save us. There are other options available, and to
discount them is downright foolish.
There are a whole lot of us out here that have opted to do other
than the mainstream medicine that's pushed daily by the industry.
One of these days, we should have a "show of hands". Perhaps
that will give some people the courage to fight for survival regardless
of the failure that they might be having with the industry's approach.
I am truly happy for all those that are alive thanks to modern medicine,
but terribly saddened by all those that I read about daily, that are dying
due to the failures of the same modern medicine.
There isn't "just one way" to fight this damned thing, and those that
encourage and perpetuate the Fear of trying something different, are
just causing the perpetuation of deaths from this malady.
Fear is never a good excuse to remain in front of a moving train,
instead of jumping off the trestle.
Stay well !!
John
John you are exactly right there FEAR nearly drove us to do something we had always said we would never do. Then faced with cancer square in the face we were scared of the what ifs. Over times as he was healing and researching we found that dr.s give those numbers no matter what. Dr.s throwing out numbers like only 40% chance of survival if he didn't do the chemo/rads. Locally they were wanting to do 6 months of chemo sandwiching the chemo/rads for 2 months. Talking to other oncologists this was WAY too much for Carls situation. So after much research, talking with specialists in differing fields we feel this is the best solution and in the back of our minds know that there is western medicine ways should we need to go that route.
Renee/Carl
9 weeks post surgery/finding out about colorectal cancer0
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