TreeHouse Foods Announces Voluntary Recall of Certain Signature Select Granola Bars

Summary Company Announcement Date: August 28, 2020
FDA Publish Date: August 28, 2020
Product Type: Food & Beverages Snack Food Item Allergens Reason for Announcement: Recall Reason Description Undeclared peanuts
Company Name: TreeHouse Foods, Inc. Brand Name: Brand Name(s) Signature Select
Product Description: Product Description Chewy Granola Bars – Chocolate Chip
Company Announcement TreeHouse Foods, Inc. (NYSE: THS) is voluntarily recalling certain Chewy Granola Bars sold under the brand name Signature Select.  This recall is being conducted because the outer carton indicates that the product is Chocolate Chip variety, while some of the individually-wrapped product contained in the carton may…

DESLORATADINE tablet [Virtus Pharmaceuticals]

Desloratadine Tablets

Read the Patient Information that comes with Desloratadine Tablets before you start taking it and each time you get a refill. There may be new information. This leaflet is a summary of the information for patients. Your doctor or pharmacist can give you additional information. This leaflet does not take the place of talking to your doctor about your medical condition or treatment.

What are Desloratadine Tablets?

Desloratadine Tablets are a prescription medicine that contains the medicine desloratadine (an antihistamine).
Desloratadine Tablets are used to help control the symptoms of:


seasonal allergic rhinitis (sneezing, stuffy nose, runny nose and itching of the nose) in people 12 years of age and older.

perennial allergic rhinitis (sneezing, stuffy nose, runny nose and itching of the nose)…

IMATINIB MESYLATE tablet, film coated [West-Ward Pharmaceuticals Corp]

6.1 Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

Chronic Myeloid Leukemia:

The majority of imatinib mesylate-treated patients experienced adverse reactions at some time. Imatinib mesylate was discontinued due to drug-related adverse reactions in 2.4% of patients receiving imatinib mesylate in the randomized trial of newly diagnosed patients with Ph+ CML in chronic phase comparing imatinib mesylate versus IFN+Ara-C, and in 12.5% of patients receiving imatinib mesylate in the randomized trial of newly diagnosed patients with Ph+ CML in chronic phase comparing imatinib mesylate and…

EVERYDAY CLEAN DANDRUFF (pyrithione zinc) shampoo [Chain Drug Consortium, LLC]

water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33 …

CARVEDILOL tablet, film coated [PD-Rx Pharmaceuticals, Inc.]

6.1 Clinical Studies Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in practice. Carvedilol has been evaluated for safety in subjects with heart failure (mild, moderate, and severe), in subjects with left ventricular dysfunction following myocardial infarction and in hypertensive subjects. The observed adverse event profile was consistent with the pharmacology of the drug and the health status of the subjects in the clinical trials. Adverse events reported for each of these patient populations are provided below. Excluded are adverse events considered too general to be informative, and…

DICLOFENAC POTASSIUM tablet, film coated [PD-Rx Pharmaceuticals, Inc.]

Cardiovascular Thrombotic Events
Clinical trials of several COX-2 selective and nonselective NSAIDs of up to three years duration have shown an increased risk of serious cardiovascular (CV) thrombotic events, including myocardial infarction (MI) and stroke, which can be fatal. Based on available data, it is unclear that the risk for CV thrombotic events is similar for all NSAIDs. The relative increase in serious CV thrombotic events over baseline conferred by NSAID use appears to be similar in those with and without known CV disease or risk factors for CV disease. However, patients with known CV disease or risk factors had a higher absolute incidence of excess serious CV thrombotic events, due to their increased baseline rate. Some observational studies found that…

RAW ANTISEPTIC HAND SANITIZER WIPES (ethyl alcohol) cloth [Raw Office Inc, The]

■ External use, not oral. Keep out of children’s reach.
■ Flammable, keep away from fire and flame.
■ Use with caution if allergic to alcohol.

When using this product

Avoid contacting face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask doctor if

■ Irritation or redness occurs.

Keep out of children’s reach.

If swallowed, get medical help or contact poison control center right away.

GLIPIZIDE AND METFORMIN HYDROCHLORIDE tablet, film coated [Teva Pharmaceuticals USA, Inc.]

Glipizide (GLIP-i-zide) and Metformin Hydrochloride (met-FOR-min hye-dro-KLOR-ide) Tablets USP

Rx only

Q1. Why do I need to take glipizide and metformin hydrochloride tablets?

Your doctor has prescribed glipizide and metformin hydrochloride tablets to treat your type 2 diabetes. This is also known as non-insulin-dependent diabetes mellitus.

Q2. What is type 2 diabetes?

People with diabetes are not able to make enough insulin and/or respond normally to the insulin their body does make. When this happens, sugar (glucose) builds up in the blood. This can lead to serious medical problems, including kidney damage, amputations, and blindness. Diabetes is also closely linked to heart disease. The main goal of treating diabetes is to lower your blood sugar to a normal level.

Q3. Why is it important to…

FAMOTIDINE tablet [PD-Rx Pharmaceuticals, Inc.]

6.1 Clinical Trial Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Famotidine was studied in 7 US and international placebo- and-active-controlled trials in approximately 2500 patients [see Clinical Studies (14)]. A total of 1442 patients were treated with Famotidine, including 302 treated with 40 mg twice daily, 456 treated with 20 mg twice daily, 461 treated with 40 mg once daily, and 396 treated with 20 mg once daily. The population was 17-91 years old, fairly well distributed between gender and race, however the predominant race…