
Prescription Drug Name:
Naproxen Sodium 220 MG
ID:
a4457b00-0430-490e-9e7e-861fa361f826
Code:
34391-3
Indications and Usage
id: bc3a85a5-6ffc-4744-a103-66460fd9f61f
displayName: INDICATIONS & USAGE SECTION
FDA Article Code: 34067-9
•minor pain of arthritis
•muscular aches
•backache
•menstrual cramps
•headache
•toothache
•the common cold
•temporarily reduces fever
Warnings
id: 0e5caf44-6192-49d1-b4c5-58be926c1ffe
displayName: WARNINGS SECTION
FDA Article Code: 34071-1
•facial swelling
•asthma (wheezing)
•shock
•skin reddening
•rash
•blisters
•have had stomach ulcers or bleeding problems
•take a blood thinning (anticoagulant) or steroid drug
•take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
•have 3 or more alcoholic drinks every day while using this product
•take more or for a longer time than directed
•right before or after heart surgery
•you have a history of stomach problems, such as heartburn
•you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
•you are taking a diuretic
•you have problems or serious side effects from taking pain relievers or fever reducers
•you have asthma
•taking any other drug
•the risk of heart attack or stroke may increase if you use more than directed or for longer than directed
•feel faint
•vomit blood
•have bloody or black stools
•have stomach pain that does not get better
•pain gets worse or lasts more than 10 days
•fever gets worse or lasts more than 3 days
•you have difficulty swallowing
•it feels like the pill is stuck in your throat
•redness or swelling is present in the painful area
•any new symptoms appear
Dosage
id: 33952703-eca2-42bb-bc52-b8039f3192ad
displayName: DOSAGE & ADMINISTRATION SECTION
FDA Article Code: 34068-7
•the smallest effective dose should be used
•drink a full glass of water with each dose
•for the first dose you may take 2 tablets within the first hour
•do not exceed 2 tablets in any 8- to 12-hour period
•do not exceed 3 tablets in a 24-hour period
•store at 20-25°C (68-77°F). Avoid high humidity and excessive heat above 40°C (104°F).
Label
id: 01fe32cb-675f-466f-8679-34e0c5bb6455
displayName: PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA Article Code: 51945-4