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Dangerous Drugs News & Drug Recalls

November 2009
Deaths, dialysis, hospitalizations reported.
October 2009
Finds fault with FDA's procedures, recommends change.
September 2009
Cataracts, endometrial cancer among other risks.
August 2009
FDA has received over 30 reports, 6 of liver failure.
July 2009
FDA has received reports of suicide in users.
June 2009
No contaminants found so far, says FDA.
May 2009
Agency offers several safety recommendations.
May 2009
Disease is serious and often permanent.
April 2009
Active ingredient dose may be incorrect.
April 2009
Chronic disease can be life-long and fatal.
April 2009
No longer available after June 8, 2009.
March 2009
Pills are oversized and can cause serious side effects.
March 2009
Diana Levine awarded $6.7 million for injuries.
January 2009
Product misrepresented to public.
December 2008
Product misrepresented to public.
December 2008
Some women on hormone therapy have twice the risk.
December 2008
Some experts want the drugs banned.
December 2008
Group thinks that ads should be removed.
December 2008
Drug increases risk by seven times.
November 2008
Dozens of deaths linked to medications.
November 2008
Increases risk of blood clots by 30%.
November 2008
Manufacturer has issued recall for 12,000 units.
November 2008
May pose life-threatening risks.
November 2008
Years after ban heart problems linger.
November 2008
Nearly 500,000 pose health risk.
November 2008
Side effects include heart attack and liver damage.
October 2008
FDA reviewing reports of more than 1,000 reactions.
October 2008
One in four required goverment regulatory action.
October 2008
Medication linked to dangerous infections.
September 2008
Medications don't have government approval.
September 2008
Agency discovered manufacturing mistakes.
September 2008
Medications linked to dangerous fungal infection.
August 2008
Woman injected with drug develops gangrene.
August 2008
FDA wants strong warnings for medication.
August 2008
FDA warns against mixing medications due to health risks.
August 2008
Plant violates manufacturing standards.
July 2008
FDA says medication illegally marketed.
July 2008
Medications cause fractures in some patients.
July 2008
15 others given overdose at same hospital.
July 2008
FDA intensifies safety warnings.
July 2008
FDA gives drugs a "black box" warning.
June 2008
Popular medication implicated in thousands of deaths.
June 2008
FDA wants warnings put on 11 drug labels.
June 2008
FDA wants warnings put on 11 drug labels.
June 2008
FDA investigates cancer risk for children.
May 2008
Pregnant women need safety information.
May 2008
Medication deemed unsafe for pilots.
May 2008
Recall continues for dangerous drug.
May 2008
Many patients do not realize that they received medication.
May 2008
Experts offer advice to patients.
May 2008
Concern over dangerous side effects growing.
May 2008
Concern over side effects growing.
April 2008
Drug sold in dangerous dosage.
April 2008
FDA investigates PA vaccine plant.
April 2008
Problems from Detrol and Ditropan.
April 2008
Med journal wants companies out.
April 2008
Fatality estimates triple.
April 2008
Over 500,000 kids injured every year.
April 2008
Arthritis medication is dangerous for some.
April 2008
Methadone linked to trend.
March 2008
Risk from asthma and allergy drug.
March 2008
Adverse reactions to Tussionex.
March 2008
Testing will begin this summer.
February 2008
Liver damage added to risks.
February 2008
Aranesp, Epogen, and Procrit.
February 2008
More patches pulled due to leak defect.
February 2008
China source of chemical.
February 2008
Overdose from Duragesic patch.
February 2008
Severe reaction reports include death.
February 2008
Meds may cause suicidal behavior.
January 2008
Treatment may lead to death.
January 2008
Thousands sent to ER every year.
January 2008
Bacterial contamination prompts lawsuits.
January 2008
Side effects of aggression and suicide.
January 2008
New study finds faster cancer risk.
January 2008
Government declares official warning.
January 2008
FDA chastises Pittsburgh pharmacy.
January 2008
Duragesic patch suspected in deaths.
January 2008
Group sues FDA for label change.
December 2007
Childhood vaccines may not be sterile.
December 2007
Sold as Carbatrol, Tegretol, and Equetro.
December 2007
Sold as DDAVP, DDVP, and Stimate.
December 2007
New risk linked to dangerous drug.
November 2007
Side effects include rash and anxiety.
November 2007
Tamiflu and Relenza might be risky.
November 2007
Study finds pills may build up plaque.
November 2007
Diabetes drug black box label updated.
November 2007
Merck tries to end painkiller litigation.
November 2007
Bayer and FDA agree to halt sales.
October 2007
Injection drug may get label changes.
October 2007
ED drugs get new label warnings.
October 2007
Companies heed warning by FDA experts.
October 2007
Serious risk from Parkinson's & RLS drug.
October 2007
Continued sales due to FDA error.
October 2007
Safety experts propose ban on drugs.
September 2007
Evidence to reveal suspect was on acne drug.
September 2007
The drug is often prescribed incorrectly.
September 2007
Findings link drug to more heart attacks.
September 2007
Reports rise 157 percent from '98 to '05.
September 2007
Undeclared ED drugs prompt recall.
August 2007
Breast milk transfer may lead to overdose.
August 2007
Diabetes drug marked due to heart risks.
July 2007
Anti-pregnancy program sees little effect.
July 2007
Dangerous drug allowed back for some patients.
July 2007
Supplement pills may cause harm.
July 2007
Two solutions have important alerts.
July 2007
Dangers may occur before 18 months.
June 2007
Early life use may have risks for kids.
June 2007
New GlaxoSmithKline study raises concerns.
May 2007
Timed-release guaifenesin lacks approval.
May 2007
Stronger warning was suggested in 2002.
May 2007
Depakote may cause mental retardation in children.
May 2007
Studies show increased heart attack and death.
May 2007
Aranesp and Procrit under fire for serious risks.
May 2007
Payout for misleading physicians and consumers.
May 2007
May cause the condition atrial fibrillation.
May 2007
Drugs to get harsher labels for increased risk.
May 2007
Fake weight loss medication and more.
April 2007
Heightened risk of heart disease.
April 2007
FDA wants age-specific warnings.
April 2007
FDA is asked to take Celebrex ad off the air.
April 2007
Heart disease and stroke increase with age.
April 2007
IBS drug causes heart attack and stroke.
March 2007
Removed due to risk of heart valve damage.
March 2007
FDA cautions online buyers.
March 2007
Advisory panels to restrict some medical experts.
March 2007
Sleeping pills may have dangerous risks.
March 2007
Takeda's pioglitazone drugs hurt bones.
March 2007
Jury orders Merck to pay heart attack victim.
March 2007
FDA warns public about side effects of ESAs.
March 2007
High caffeine levels cause sickness.
March 2007
Over-the-counter cold drugs could harm young children
March 2007
Antibiotic has deadly side effects for some patients.
February 2007
Xolair may lead to anaphylaxis in allergy patients.
February 2007
FDA requests Patient Medication Guides from manufacturers.
February 2007
FDA warns about false Internet marketing of powerful drugs.
February 2007
Children's vaccine may lead to serious intestinal condition.
February 2007
FDA places "black box" label on drug with serious side effects.
February 2007
Increase coincides with FDA black-box warning.
February 2007
Clot risk doubles with low-dose pills.
February 2007
Projects would allow the FDA to better oversee drugs already on the market.
January 2007
Wyeth ordered to pay $1.5 million.
January 2007
Increase in fees could mean more responsibilities for the FDA.
January 2007
The term "natural" does not ensure safety.
January 2007
Two Cox-2 drugs will seek U.S. FDA approval.
January 2007
During a two-year period, more than 1,500 children under two years old were taken to ERs because of serious reactions to cold and cough medications.
January 2007
Two drugs linked to higher risk of heart-valve damage.
January 2007
Fatal viral infection associated with the drug, Rituxan.
December 2006
Study results call into question the safety of heartburn drugs.
December 2006
Labels may soon be changed cause drugs are more dangerous than previously thought.
December 2006
Internal documents show Lilly played down risks and promoted off-label use.
December 2006
New labels may warn of suicide dangers to adults up to age 24.
December 2006
FDA concludes young users have more risks for suicidal behavior.
December 2006
FDA believes drug-coated stents pose a risk of death and raise other safety concerns.
December 2006
Torcetrapib trials end in more deaths than expected.
December 2006
If pregnant or planning to become pregnant, do not use Paxil.
November 2006
FDA panel to decide if label changes or further studies need to take place.
November 2006
New pain reliever has risks like Vioxx.
November 2006
FDA suggests label change after Japan's reports.
November 2006
About 11 million bottles containing acetaminophen 500mg caplets are affected by the recall.
November 2006
Forty-four women sue Orth-McNeil.
October 2006
Reports indicate that Ritalin in young children has risks.
October 2006
Over 700,000 trips to the ER are a result of common medications.
October 2006
Institute of Medicine makes recommendations to the FDA.
October 2006
FDA's limited budget could result in greater public health risks.
October 2006
Jury finds Prempro led to woman's breast cancer.
October 2006
Bayer conducted study and knew of risks.
September 2006
Data about blood clot risks from two studies put on label.
September 2006
Over 2% of all prescription drugs are not approved by the FDA.
September 2006
Users required to follow a series of rules before getting a prescription filled.
September 2006
FDA whistle-blower claims drug may be just as dangerous.
September 2006
FDA to see if benefits outweigh the risks of the antibiotic, Factive.
September 2006
Two Canadian websites selling counterfeit drugs to U.S. consumers.
August 2006
Agency committees don't reject new drugs or medical devices often.
August 2006
Stronger warning labels will be put on Adderall,Ritalin and Concerta.
August 2006
Lawsuits raise concerns about who the FDA is really looking out for.
August 2006
Accutane raises risk for potential heart attacks or liver problems.
August 2006
New Orleans jury awards $51 million to Vioxx heart attack victim.
August 2006
FDA warns three pharmacies of being in violation of federal law.
August 2006
WellPatch vapor pads recalled for potentially serious health risks.
July 2006
Millions of patients each year are given the wrong medications.
July 2006
The cancer drug treatment, Gleevec, has been linked to heart risks.
July 2006
Combination of the two types of drugs can lead to serotonin syndrome.
July 2006
Internal documents indicate that not all officials agreed with the drug's approval.
July 2006
Commonl used antibiotic has been linked to serious diabetic diseases.
July 2006
New rule would require study sponsors to report anyone who has committed fraud in a trial.
July 2006
New England JOurnal of Medicine removes 18-months or longer statements from their publication.
July 2006
Study showed abnormal liver test results in one of five healthy adults who took four grams of Tylenol daily for two weeks.
July 2006
Thirteen patients taking the Aptivus HIV drug suffered bleeding on the brain, resulting in eight deaths.
June 2006
Drug causes liver failure almost four times as often as other antibiotics.
June 2006
FDA issues consumer warning about reactions to the vapor patches.
June 2006
Study finds drugs cause birth defects even in the first trimester.
June 2006
Doctors group believes a delay of consumer ad campaigns would give doctors more to study the products
June 2006
Medicines containing carbinoxamine are not all FDA approved.
May 2006
Supports claims Vioxx causes heart problems.
May 2006
National estimates say ADHD drugs likely send thousands to emergency rooms.
May 2006
Ketek linked to cases of liver failure.
May 2006
Infections from rheumatoid arthritis drugs.
May 2006
A GlaxoSmithKline study found that Paxil increases adult suicide risk.
May 2006
FDA-approved does not necessarily mean a drug is safe.
May 2006
Atypicals are approved for adults, but are being used to treat children with mental illnesses.
May 2006
The FDA approved the antibiotic Ketek despite flawed studies.
January 2001
Our law firm was among the first to file a Lotronex lawsuit against Glaxo-Wellcome.
June 2005
Painkiller’s packaging contained confusing information.
February 2005
Vioxx study links drug to more heart attacks
February 2005
Merck cancelled an early study of the heart risks associated with Vioxx, that could have potentially saved lives and prevented serious cardiovascular disease.
June 2005
Generic drugs might not have the same label information as name-brand drugs.
April 2006
New Jersey jury orders Merck to pay punitive damages.
April 2006
Jury awards plaintiff $3 million in compensatory damages for heart attack caused by Vioxx.
July 2005
Prescription painkiller has serious side-effects when combined with alcohol.
January 2006
Merck will return to court for their fourth Vioxx trial.
February 2005
Studies show the painkiller doubled the risk of heart attacks and strokes.
March 2005
Cox-2 Inhibitors required by the FDA to carry black box warnings. Find out more.
August 2005
Foreign drugs may have different ingredients than their American counterparts.
November 2005
Doctors stop writing prescriptions for the Orth-Evra birth control patch.
December 2005
Certain eye drops and pain medications by Molecular Biologics Inc. should be discarded immediately.
May 2005
A public interest group criticizes the FDA for not pulling drug from the market.
January 2006
Two more deaths have been linked to the drug used to treat heart failure patients.
October 2005
Cymbalta may make liver conditions worse.
December 2005
Drug companies still aren?t telling consumers the whole story.
December 2005
The FDA classifies Paxil as a "Category D" drug.
December 2004
Most Neurontin prescriptions are for off-label uses such as treatment of bipolar disorder. Could this lead to suicide as an alleged side effect?
February 2006
Some drugs approved by the FDA are harmful.
March 2006
FDA criticized for delay in 65 percent of drug trials.
October 2005
Study indicates an increase of birth defects in babies born to women using Paxil.
December 2005
FDA pulls imaging agent, NeutroSpec, after reports of serious reactions.
March 2006
FDA urged to ban the pain reliever, Darvocet.
November 2005
Study reports patients and doctors don?t comply with the “black box” warnings.
August 2005
FDA imposes strict guidelines on how Accutane and its generic version are prescribed.
February 2005
Antidepresants including Zoloft have been linked to increases in suicidial behavior among children and teenagers.
August 2005
Pfizer will no longer promote any of its new drugs until they have been on the market for six months.
July 2005
FDA investigates reports of fatal overdoses from pain patch.
January 2006
Elidel and Protopic get "black box" labels because of potential cancer risks associated with the drugs.
February 2006
FDA advisory committee recommends ADHD drugs carry a "black-box" warning.
December 2005
Study shows older antipsychotics are more dangerous to the elderly than newer drugs.
November 2005
FDA requires drug companies to submit digital medication labels.
October 2005
Boston Scientific Corp. halts sales of the Enteryx drug injection kit.
March 2006
Study finds Plavix offers no real benefit over low-dose aspirin treatment, but can cause bleeding.
February 2006
Users of the patch double their risk of blood clots and other serious side effects.
March 2006
ADHD medication may have to provide more detailed information about the risk risk of mania and psychosis.
April 2006
Evidence shows that this combined use of hormone replacement therapy has risks of its own.
March 2006
FDA advisory panel decides 'black-box" warning does not need to go on ADHD drugs.
May 2005
A new report shows increased links between hormone replacement therapy and recurring breast cancer.
November 2005
Women using Ortho Evra birth control patch exposed to 60 percent more estrogen than the pill.
October 2005
Some patients hospitalized with worsened conditions, a symptom of incorrect medications.
July 2005
FDA orders labels on certain ADHD medications indicate a possibility of psychiatric side effects.
February 2006
Life-threatening risk caused by drug's effect on blood sugar.
July 2005
Urges patients to be monitored closely for warning signs of suicide.
February 2006
Antidepressants may increase the chance of an infant contracting the lung disorder, persistent pulmonary hypertension.
June 2005
Babies born to women taking antidepressants during pregnancy have a greater chance of developing drug-related symptoms.
February 2005
Vioxx and other Cox-2 inhibitors can cause a rare yet serious side effect, a skin disease called Stevens Johnson Syndrome.
May 2005
The FDA has issued “black box” warnings on seven antipsychotic drugs used to treat behavioral problems in elderly patients with dementia.
February 2006
From 1999 through 2003, 25 people died and 54 others had unexplained heart problems while taking stimulants.
September 2005
FDA issues warning children using Strattera for ADHD may have suicidal thoughts.
March 2006
FDA issues warning to companies selling dietary supplements with synthetic steroids.
October 2005
Use of the drugs to treat childhood depression is declining.
November 2005
FDA issues warning about three medications used to treat asthma.
April 2006
Merck's Fosamax linked to rare jawbone disease.
January 2006
Resources that can help keep you safe.
January 2006
Trasylol linked to increased risk of kidney failure, heart attacks and strokes.
January 2006
Off-label use of NovoSeven can lead to serious health problems.
February 2005
Study finds Alzheimer's patients using Celebrex to be up to four times more likely to exhibit cardiovascular risk factors than those taking a placebo.
March 2006
FDA hears testimonies from MS patients who want Tysabri back on the market.
February 2005
"Compelling" evidence of heightened heart risks prompts Kaiser Permanente to stop prescribing Bextra.
February 2006
FDA to decide if the MS drug, Tysabri, should be put back on the market.
February 2005
Doctors continue to prescribe dangerous medication to patients.
March 2006
FDA advisory panel votes to put Tysabri back on the market.
November 2005
Concerns about commercial hormones have lead women to plant hormones.
May 2005
More needs to be done to educate physicians, patients and pharmacists about the potential dangers of prescription drugs.
September 2005
FDA reports indicate Tysabri usage linked to serious, nonfatal infections.
December 2005
ER visits for heart attack sufferers could result in an increased risk of serious bleeding.
January 2006
The FDA warns consumers not to use Brazilian diet pills.
October 2005
Viagra and other impotence drugs could cause blindness.
December 2005
FDA warns that Campath should not be used to treat multiple sclerosis.
May 2005
Reports of partial vision loss in 38 men have prompted the FDA to request a change to drug labels.
May 2005
Confidential company documents, detail the aggressive tactics of a sales army who pushed the arthritis drug.
May 2006
Pfizer brings back Celebrex ads in hopes to boost sales.
August 2005
For those injured after taking Vioxx, a settlement without a trial may be possible.
February 2006
Pfizer's first Celebrex trial set to begin in June.
August 2005
Label cautions about increased risk of heart attacks and strokes.
December 2005
Third Vioxx trial ends in mistrial after jurors couldn't reach verdict.
February 2006
Retrial begins in the first Federal Vioxx case.
January 2006
Six heart attack patients died as a result of the dietary supplement, L-arginine.
October 2005
Research shows confusion about meanings of prescription drug labels.
May 2006
Merck's defense shaken with Canadian Medical Association Journal's Vioxx study.
January 2006
FDA has designed a new look for drug labels.
April 2006
Fatal heart attack victim took Vioxx for less than one month.
March 2006
Two New Jersey men suing Merck for heart attacks suffered after long-term use of Vioxx.

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