Ranitidine Warnings

The United States Food and Drug Administration FDA Puts Out Warning for Ranitidine Users

In early April 2020, the U.S. Food and Drug Administration FDA warned that Zantac ranitidine’s over-the-counter heartburn medication was unsafe. The FDA said this because all ranitidine products contain unacceptable levels of NDMA (N Nitrosodimethylamine).

When N Nitrosodimethylamine NDMA breaks down, ranitidine drugs can lead to cancer or probable human carcinogen if the levels of NDMA build up too much, so you should talk to a health care professional about prescriptions and the FDA recall.

Talk to a personal injury attorney at Rosenfeld Injury Lawyers, LLC, today at (999) 424-5757 (toll-free phone call) or use the contact form to learn what you could receive in a possible jury award or settlement via a ranitidine lawsuit.

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Zantac ranitidine and other ranitidine meds treat gastroesophageal reflux disease, lower stomach acid, and reduce coughing. Since this H2 blocker has too high levels of NDMA, the FDA has issued a recall to all patients for this OTC medication.

If you’re taking OTC ranitidine, you should stop and contact a doctor for advice. The medic will advise you about using an alternative over-the-counter Ranitidine, especially if you’re taking other medications.

Talk to Our Experts About the Health Risks Associated with Over the Counter Zantac Ranitidine Medications

The FDA recall protects patients from cancer risk since the drug manufacturers put NDMA in Zantac ranitidine drug. Many consumers and patients did not know this OTC heartburn med had a high level of NDMA or at least unacceptable levels.

Consumer exposure to unacceptable levels of NDMA in Ranitidine or all ranitidine heartburn-relieving products can harm them seriously.

Suppose you have questions about ranitidine medication, the FDA market withdrawal request, NDMA human carcinogen, and cancer risk from Zantac ranitidine or other ranitidine products. In that case, talk to our ranitidine product experts about consumers’ rights regarding a wrong medication.

Ranitidine adverse effects include stomach pain, diarrhea, nausea, headache, dry mouth, and dizziness. Allergic reactions are no rare side effects of Ranitidine. It is estimated that about 1% of the general population will suffer from a drug allergy in their life.

Ranitidine, a popular anti-acid medication, may cause severe chest pain in some people who suffer from mitral valve prolapse. The FDA recommends patients and healthcare professionals take caution and be aware of what is currently known about Ranitidine.

What Do Ranitidine Medicines Do, and Why Do Patients Take These Market Products?

Ranitidine medicines, including prescription ranitidine products, are known as H2 blockers. They lower the level of acid that your stomach produces.

It has several great benefits, including the following:

  • Stop heartburn
  • Reduce coughing and swelling
  • Lower acid levels throughout your GI tract
  • Stop gastroesophageal reflux disease (GERD)

Unfortunately, drug evaluation and researchers at the FDA and other health care professionals have discovered that NDMA in the market makes it unsafe even when kept in storage conditions at room temperature or higher than room temperatures. The low levels of NDMA can break down and develop into a probable human carcinogen.

The drug interactions of Zantac ranitidine are primarily with drugs that are metabolized by the liver, or it can affect how the kidneys filter out those drugs. If you experience chest pain, dark urine, and bloody stool after using Ranitidine, you should consult your doctor immediately.

Drugs Precautionary Use

Ranitidine tablet overdose symptoms may include rash, diarrhea, drowsiness, and fever. Measure liquid medicine carefully to get the right next dose at the right time. If you suspect someone has overdosed on a potentially hazardous drug, immediately contact your local poison control center.

Being on the Lookout for Ranitidine Food Interaction

A patient’s medical history and current list of medications should be reviewed to look for possible drug-drug and drug-food interactions. The laboratory tests on this medication include those that measure the levels of Ranitidine in the blood and those that determine if there is any reaction to this medication.

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Seeking Medical Advice Before Consuming Ranitidine

You should consult a healthcare professional before taking Ranitidine if you are pregnant or breastfeeding. It’s essential to notify your doctor if you’re taking dietary supplements, especially if they’re new to you or contain caffeine because they could interact with your regular medications.

If you’re taking herbal products, such as chamomile, turmeric, garlic, and ginger, you should speak to your doctor before consuming Ranitidine (Zantac, Zantac EFFERDOSE). Taking these herbal supplements along with Ranitidine might cause your body to absorb less of Ranitidine, reducing its effectiveness.

Ranitidine Side Effects

Taking prescription-strength Ranitidine (Zantac) can cause serious side effects, including life-threatening ones. Before taking Taking prescription-strength Ranitidine, be sure to tell your doctor about any allergies or sensitivities you have, as well as all other medications you may be taking.

Taking Zantac 300 mg can lead to serious side effects. Ranitidine has been associated with liver toxicity, though this is rare and usually only happens in those who consume alcohol in excess. Avoid drinking alcohol while taking Ranitidine.

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Ranitidine Warning Label

Many ranitidine medications carry a black box warning about the risks of renal impairment due to Ranitidine.

Notifying the Medical Personnel You are on Ranitidine Before they Treat You

Tell the laboratory personnel, doctor, or pharmacist that you are on Ranitidine before any lab tests, X-rays, or surgery. Ranitidine can affect your test results.

The drug information is critical when seeking emergency medical help because a doctor can administer treatment to counter the effects of overconsumption before a patient goes into cardiac arrest or shock.

Taking Inappropriate Dosage

According to a study published by JAMA Internal Medicine, a medicine dose-measuring device used in the home to help people measure the amount of a drug they are taking may not be accurate.

Taking over-the-counter medication to relieve pain is not advised for certain people with mental health problems because it will be challenging to ensure they take the correct dose.

 Ranitidine 150 mg Dosage for Treating Stomach Acid

Ranitidine 150 mg (brand name Zantac) is an antacid used to treat conditions involving excess stomach acid, gastroesophageal reflux disease, peptic ulcers, Hiatal hernias, and esophageal cancer. A doctor or pharmacist may prescribe 150 mg of Ranitidine and then increase the dosage — after a period of observation — to 300 mg.

Ranitidine 150 mg is used to treat ulcers for four weeks. Ranitidine 150 mg can also be used for the treatment of kidney disease.

Accounting for the Missed Dosage

Taking Ranitidine 150 mg on time is essential, but it’s not advisable to take it alongside the missed dose. Do not try to make up for the missed dose by taking two doses at once during your next dose. Surpassing 150 mg of Ranitidine in a day can lead to serious harm, even death.

Allergic Response Due to Ranitidine

An allergic reaction due to Ranitidine 150 mg, an acid-reducing drug, was reported by a patient in France. The patient was prescribed ranitidine 150 mg to be taken orally twice daily.

He experienced an itchy skin rash when he first took the drug, but he retook it due to his high blood pressure. Two days after retaking the drug, he experienced a severe allergic reaction – difficulty breathing and an itchy skin rash.

The patient was treated with diphenhydramine and hemodialysis, and he is recovering.

Call emergency medical help (911) if you have any unusual symptoms that may signal a severe allergic reaction, such as hives, difficulty breathing, or swelling of your face, lips, tongue, or throat.

Ranitidine 300 mg tablet

Ranitidine 300 mg tablet is used to treat heartburns. However, some doctors are now warning their patients to stop taking the drug if they experience any of these symptoms:

  • Severe muscle pain in arms or legs
  • Seizures
  • Painful red spots on the skin
  • Unexplained bleeding
  • Inability to urinate

In addition, Ranitidine 300 mg is prescribed to reduce stomach acid and to treat conditions such as gastroesophageal reflux disease (GERD), peptic ulcer disease, and Zollinger-Ellison syndrome symptoms including severe ulcers.

You should call your doctor if symptoms worsen or persist despite treatment with Ranitidine 150mg, 300mg, or 150mg/30ml oral suspension (150mg per 5ml).

Although OTC ranitidine relieves heartburn symptoms, indigestion, acid reflux, and hiatal hernia, it may have serious side effects on the liver. Ranitidine oral solution should be measured with the aid of a dosing syringe provided to ensure accurate dosing

Call your Doctor or Pharmacist If Your Condition Worsens After Taking Ranitidine 300mg

You should call your doctor if you experience any of the following symptoms when taking Ranitidine 300 mg:

  • Black, tarry stools
  • Blood in urine or under the skin
  • Frequent nausea or vomiting

The use of Ranitidine worsens some medical conditions. Therefore, patients should let their doctor know if they have these conditions or take any other medicines.

Stomach Acid Conditions Requiring Ranitidine Medication

Patients use Ranitidine to contain too much acid in the stomach or instances in which acid retracts to the esophagus. An OTC stomach acid medicine is a drug sold without a prescription.

It does not require a doctor’s care and monitoring while using it. It’s advisable to consult a doctor before using an OTC stomach acid medicine if you’re expecting.

Too much acid in the stomach is usually not good, and millions of people experience it every day. The stomach pain problems of patients taking Ranitidine often don’t get reported until too late.

The stomach produces a large amount of acid daily. If the acid levels get too high, it can lead to an ulcer.

Generic drugs prices are the only factor influencing patient adherence to their prescribed medication regimen. The use of Ranitidine may mimic early symptoms of gastric ulceration.

Suppose you have liver disease or are suffering from certain mental health disorders. Consult your doctor before taking this medication.

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The FDA Market Recall in 2020

In early April 2020, Janet Woodcock of the FDA issued a warning that prompted this ranitidine product to be taken back to a drug take-back location site. Specifically, it stated that low levels or just a low level of NDMA make it unsafe when at normal or higher than room temperatures.

This FDA market pronouncement affected millions of people who take these drugs or products at low levels or beyond the intake limit.

Understandably, they were concerned the OTC medicine might cause cancer. It caused a dramatic reversal almost overnight.

The Food and Drug Administration issued an immediate market withdrawal request for Ranitidine 150 mg sold by pharmacies and a warning about Ranitidine 75 mg sold at drugstores.

The FDA requested the market withdrawal of Ranitidine 150 mg after finding out that some batches from one or more Ranitidine manufacturers may have been contaminated with a widely used veterinary antibiotic.

The FDA is working with Ranitidine and veterinary drug manufacturers to remove the contaminated products from the market.

The FDA Other Approved OTC Products to Treat Gastric Acid

Besides Ranitidine, other FDA approved drugs to treat ulcers include:

  • Pantoprazole 20mg
  • Esomeprazole 40mg
  • Lansoprazole 15mg
  • Omeprazole 20mg
  • Rabeprazole 10mg
  • Dexlansoprazole 30mg

The Food and Drug Administration ensures that other drugs warnings are provided. As Zantac ranitidine contains the active ingredient ranitidine, it should be no surprise that it has several warnings, including for pediatric patients.

According to a warning by the U.S. Food and Drug Administration, patients taking prescription Ranitidine are being advised to monitor their blood levels of the drug. The FDA announced that Ranitidine, sold under the brand name Zantac, may not effectively lower blood levels of the drug in some patients.

The FDA approves multiple drugs to treat gastroesophageal reflux disease (GERD), but ranitidine (Zantac, GlaxoSmithKline, Research Triangle Park, NC) is the only one that can reduce the production of gastric acid.

Ranitidine belongs to the class of drugs called H2-receptor antagonists, and it works by blocking histamine receptors in the stomach.

You should call your doctor if new or existing prescriptions don’t seem to be working.

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Take Action by Bringing a Case

So far, there have been many lawsuits brought by individuals harmed due to this announcement. They are a part of an MDL in Florida and a few class-action lawsuits brought in Connecticut, New Jersey, and California.

If you took these meds and were damaged, you should consider the same.

  • Plaintiffs that bring cases may achieve different kinds of relief and compensation. First, you may obtain money back for the defective meds you bought.
  • Second, you may be able to recover nominal sums for the deficient warning that the pills had on the label.
  • Third, you could even possibly get damages for your pain, suffering, medical expenses, shortened lifespan, and cancer diagnosis.

Hire a Zantac Injury Lawyer to Resolve Your Dangerous Drug Compensation Case

Rosenfeld Injury Lawyers LLC represents victims after being injured from defective pharmaceuticals on a contingency fee basis. If you have taken these over-the-counter heartburn medications, let us know to see if we can help you. Many people are discovering that relief and compensation are available, and it may be for you as well.

Our team of legal experts and attorneys work on contingency, so you do not have to worry about any bill until you get a Zantac award or settlement. Start the process now by calling our offices toll-free at (888) 424-5757 and seeing what you need to do to get back on track.


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