Prescription Drug Information: Fenoprofen Calcium (Page 4 of 4)

16. HOW SUPPLIED/STORAGE AND HANDLING

Fenoprofen calcium® (fenoprofen calcium, USP) are available in capsule form for oral administration, and are supplied as following:
● The 200 mg capsule has an opaque orange cap with an opaque white body imprinted with “RX681” and is 23mm long.

.

Storage:
Store at room temperature 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].
Preserve in well-closed containers

17. PATIENT COUNSELING INFORMATION

Advise the patient to read the FDA-approved patient labeling (Medication Guide) that accompanies each prescription dispensed. Inform patients, families, or their caregivers of the following information before initiating therapy with FENOPROFEN CALCIUM and periodically during the course of ongoing therapy.

Cardiovascular Thrombotic Events

Advise patients to be alert for the symptoms of cardiovascular thrombotic events, including chest pain, shortness of breath, weakness, or slurring of speech, and to report any of these symptoms to their health care provider immediately [ see Warnings and Precautions ( 5.1) ].

Gastrointestinal Bleeding, Ulceration, and Perforation
Advise patients to report symptoms of ulcerations and bleeding, including epigastric pain, dyspepsia, melena, and hematemesis to their health care provider. In the setting of concomitant use of low-dose aspirin for cardiac prophylaxis, inform patients of the increased risk for and the signs and symptoms of GI bleeding [ see Warnings and Precautions ( 5.2) ].

Hepatotoxicity
Inform patients of the warning signs and symptoms of hepatotoxicity (e.g., nausea, fatigue, lethargy, pruritus, diarrhea, jaundice, right upper quadrant tenderness, and “flu-like” symptoms). If these occur, instruct patients to stop FENOPROFEN CALCIUM and seek immediate medical therapy [ see Warnings and Precautions ( 5.3) ].

Heart Failure and Edema
Advise patients to be alert for the symptoms of congestive heart failure including shortness of breath, unexplained weight gain, or edema and to contact their healthcare provider if such symptoms occur [ see Warnings and Precautions ( 5.5) ].

Anaphylactic Reactions
Inform patients of the signs of an anaphylactic reaction (e.g., difficulty breathing, swelling of the face or throat). Instruct patients to seek immediate emergency help if these occur [ see Contraindications ( 4) and Warnings and Precautions ( 5.7) ].

Serious Skin Reactions
Advise patients to stop FENOPROFEN CALCIUM immediately if they develop any type of rash and to contact their healthcare provider as soon as possible [ see Warnings and Precautions ( 5.9) ].

Female Fertility
Advise females of reproductive potential who desire pregnancy that NSAIDs, including FENOPROFEN CALCIUM, may be associated with a reversible delay in ovulation [ see Use in Specific Populations ( 8.3) ]

Fetal Toxicity
Inform pregnant women to avoid use of FENOPROFEN CALCIUM and other NSAIDs starting at 30 weeks gestation because of the risk of the premature closing of the fetal ductus arteriosus [ see Warnings and Precautions ( 5.10) and Use in Specific Populations ( 8.1) ].

Avoid Concomitant Use of NSAIDs
Inform patients that the concomitant use of FENOPROFEN CALCIUM with other NSAIDs or salicylates (e.g., diflunisal, salsalate) is not recommended due to the increased risk of gastrointestinal toxicity, and little or no increase in efficacy [ see Warnings and Precautions ( 5.2) and Drug Interactions ( 7) ]. Alert patients that NSAIDs may be present in “over the counter” medications for treatment of colds, fever, or insomnia.

Use of NSAIDS and Low-Dose AspirinInform patients not to use low-dose aspirin concomitantly with FENOPROFEN CALCIUM until they talk to their healthcare provider [ see Drug Interactions ( 7) ].

Medication Guide

What is the most important information I should know about medicines called Nonsteroidal Anti-inflammatory Drugs (NSAIDs)? NSAIDs can cause serious side effects , including:

Increased risk of a heart attack or stroke that can lead to death. This risk may happen early in treatment and may increase:

  • with increasing doses of NSAIDs
  • with longer use of NSAIDs Do not take NSAIDs right before or after a heart surgery called a “coronary artery bypass graft (CABG).” Avoid taking NSAIDs after a recent heart attack, unless your healthcare provider tells you to. You may have an increased risk of another heart attack if you take NSAIDs after a recent heart attack.

Increased risk of bleeding, ulcers, and tears (perforation) of the esophagus (tube leading from the mouth to the stomach), stomach and intestines:

  • anytime during use o without warning symptoms
  • that may cause death

The risk of getting an ulcer or bleeding increases with

  • past history of stomach ulcers, or stomach or intestinal bleeding with use of NSAIDs
  • taking medicines called “corticosteroids”, “anticoagulants”, “SSRIs”, or “SNRIs”
  • increasing doses of NSAIDs
  • older age
  • longer use of NSAIDs
  • poor health
  • smoking
  • advanced liver disease
  • drinking alcohol
  • bleeding problems

NSAIDs should only be used:

  • exactly as prescribed o at the lowest dose possible for your treatment
  • for the shortest time needed

What are NSAIDs? NSAIDs are used to treat pain and redness, swelling, and heat (inflammation) from medical conditions such as different types of arthritis, menstrual cramps, and other types of short-term pain.

Who should not take NSAIDs? Do not take NSAIDs:

  • if you have had an asthma attack, hives, or other allergic reaction with aspirin or any other NSAIDs.
  • right before or after heart bypass surgery.

Before taking NSAIDs, tell your healthcare provider about all of your medical conditions, including if you:

  • have liver or kidney problems
  • have high blood pressure
  • have asthma
  • are pregnant or plan to become pregnant. Talk to your healthcare provider if you are considering taking NSAIDs during pregnancy. You should not take NSAIDs after 29 weeks of pregnancy.
  • are breastfeeding or plan to breast feed.

Tell your healthcare provider about all of the medicines you take, including prescription or over-the-counter medicines, vitamins or herbal supplements. NSAIDs and some other medicines can interact with each other and cause serious side effects. Do not start taking any new medicine without talking to your healthcare provider first.

What are the possible side effects of NSAIDs? NSAIDs can cause serious side effects, including

  • new or worse high blood pressure
  • heart failure
  • liver problems including liver failure
  • kidney problems including kidney failure
  • low red blood cells (anemia)
  • life-threatening skin reactions
  • life-threatening allergic reactions

Other side effects of NSAIDs include: stomach pain, constipation, diarrhea, gas, heartburn, nausea, vomiting, and dizziness.

Get emergency help right away if you get any of the following symptoms

  • shortness of breath or trouble breathing
  • slurred speech
  • chest pain
  • swelling of the face or throat
  • weakness in one part or side of your body

Stop taking your NSAID and call your healthcare provider right away if you get any of the following symptoms:

  • nausea
  • vomit blood
  • more tired or weaker than usual
  • there is blood in your bowel movement or it is
  • diarrhea black and sticky like tar
  • itching
  • unusual weight gain
  • your skin or eyes look yellow
  • skin rash or blisters with fever
  • indigestion or stomach pain
  • swelling of the arms, legs, hands and feet
  • flu-like symptoms

If you take too much of your NSAID, call your healthcare provider or get medical help right away.

These are not all the possible side effects of NSAIDs. For more information, ask your healthcare provider or pharmacist about NSAIDs. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Other information about NSAIDs:

Aspirin is an NSAID but it does not increase the chance of a heart attack. Aspirin can cause bleeding in the brain, stomach, and intestines. Aspirin can also cause ulcers in the stomach and intestines. Some NSAIDs are sold in lower doses without a prescription (over-the-counter). Talk to your healthcare provider before using over-the-counter NSAIDs for more than 10 days.

General information about the safe and effective use of NSAIDs Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use NSAIDs for a condition for which it was not prescribed. Do not give NSAIDs to other people, even if they have the same symptoms that you have. It may harm them. If you would like more information about NSAIDs, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about NSAIDs that is written for health professionals.

Package Label

label
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400

300
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300

502
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FENOPROFEN CALCIUM fenoprofen calcium capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0276-0503
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FENOPROFEN CALCIUM (FENOPROFEN) FENOPROFEN 400 mg
Inactive Ingredients
Ingredient Name Strength
CROSPOVIDONE
MAGNESIUM STEARATE
SODIUM LAURYL SULFATE
TALC
GELATIN
TITANIUM DIOXIDE
BROWN IRON OXIDE
Product Characteristics
Color yellow (opaque) , white (opaque) Score no score
Shape CAPSULE Size 23mm
Flavor Imprint Code RX681
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0276-0503-90 90 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA017604 11/01/2021 02/20/2022
FENOPROFEN CALCIUM fenoprofen calcium capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0276-0502
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FENOPROFEN CALCIUM (FENOPROFEN) FENOPROFEN 300 mg
Inactive Ingredients
Ingredient Name Strength
CROSPOVIDONE
MAGNESIUM STEARATE
SODIUM LAURYL SULFATE
TALC
GELATIN
TITANIUM DIOXIDE
BROWN IRON OXIDE
Product Characteristics
Color yellow (opaque) , white (opaque) Score no score
Shape CAPSULE Size 23mm
Flavor Imprint Code RX681
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0276-0502-10 100 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA017604 11/01/2021 02/20/2022
FENOPROFEN CALCIUM fenoprofen calcium capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0276-0501
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FENOPROFEN CALCIUM (FENOPROFEN) FENOPROFEN 200 mg
Inactive Ingredients
Ingredient Name Strength
CROSPOVIDONE
MAGNESIUM STEARATE
SODIUM LAURYL SULFATE
TALC
GELATIN
TITANIUM DIOXIDE
BROWN IRON OXIDE
Product Characteristics
Color orange (opaque) , white (opaque) Score no score
Shape CAPSULE Size 23mm
Flavor Imprint Code RX681
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0276-0501-10 100 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA017604 11/01/2021
Labeler — Misemer Pharmaceuticals, Inc. (784121365)

Revised: 02/2022 Misemer Pharmaceuticals, Inc.

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