FROM OUR EXPERTS
This question has not been answered by one of our experts yet.
Generic Name: GUAIFENESIN/DEXTROMETHORPHAN/DECONGESTANT -
ORAL Cough & Cold Mucus Relief CF Oral Precautions
Before taking this combination medication, tell your
doctor or pharmacist if you are allergic to any of the ingredients; or if you
have any other allergies. Also tell your doctor if you have had a bad reaction
to decongestants (such as ephedrine, phenylephrine, pseudoephedrine). This
product may contain inactive ingredients, which can cause allergic reactions or
other problems. Talk to your pharmacist for more details.
Before using this medication, tell your doctor or
pharmacist your medical history, especially of:
breathing problems (such as emphysema, chronic bronchitis,
asthma, smoker's cough)
cough with blood or large amounts of mucus
high blood pressure
heart disease (such as chest pain, heart failure, heart
a certain eye problem (glaucoma)
We have almost made it through the last of outdoor allergy season. Ragweed has run its course in most of the U.S. while mold spores try to survive the declining temperatures of the Midwest and Northeast. Currently outdoor mold, weather changes and shared germs are leading factors in the escalation of cough, wheezing, runny nose and sinus congestion plaguing many of us. Although many areas of the country will soon see a dramatic decline in outdoor mold counts as the first hard frost approaches, the common cold virus is here to wreak havoc for several more months.
As a parent, I know there is nothing more frustrating than hearing your child cough all night. During the fall and winter months, the common cold virus is often the culprit responsible for upper respiratory tract infections and asthma attacks in adults and children. Stopping the cough becomes a main goal for surviving work, school and sleep time.
The Chicago Tribune published an article about the shortcomings of ...
What exactly is a "black box" warning? Simply put, it's the strongest warning that the U.S. Food and Drug Administration (FDA) can require on a drug's packaging. The FDA requires the black box warning when studies suggest a drug can cause a serious or life-threatening side effect. The text of the warning is set apart from other information in a black box, so that doctors, pharmacists, and patients can easily see it. What did the FDA advisory panel recommend? The FDA itself hasn't made a decision about acetaminophen, but an FDA advisory panel has made 10 recommendations concerning the drug. Among those recommendations, the panel voted to remove acetaminophen-containing painkillers such as Vicodin, Tylenol 3, and Percocet from the nation's formularies. It also voted in favor of removing all acetaminophen-containing prescription drugs from the market. But the panel voted to keep over-the-counter (OTC) pills that combine acetaminophen and other ingredients, su...
You should know
Answers to your question are meant to provide general health information but should not replace medical advice you receive from a doctor. No answers should be viewed as a diagnosis or recommended treatment for a condition. Content posted by community members does not necessarily reflect the views of Remedy Health Media, which also reserves the right to remove material deemed inappropriate.