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Important Note
The following information is intended to supplement, not substitute for, the expertise and judgment of your doctor. It should not be construed to indicate that use of Flextra DS is safe, appropriate, or effective for you. Consult your doctor before using Flextra DS.
Taking Flextra DS
Flextra DS should be taken by mouth, usually every 4 hours as needed or as directed by your doctor. The dosage is based on your age, medical condition, and response to therapy.
Do not exceed the recommended dosage or take Flextra DS for longer than recommended (e.g., 10 days for adults, 5 days for children, or 3 days if used for fever).
Persistent symptoms of pain or fever may be the sign of a more serious medical condition, consult your doctor if this is the case.
Side Effects
Flextra DS may cause drowsiness or nausea to occur. If either of these effects persist or worsen, notify your doctor promptly.
Tell your doctor immediately if any of these unlikely but serious side effects occur: skin redness, swelling, persistent fever, stomach pain, yellowing eyes and skin, dark urine, unusual weakness. If you notice other effects not listed above, contact your doctor or pharmacist.
Precautions
Tell your doctor your medical history, especially of: lung problems (e.g., bronchitis, emphysema), glaucoma, enlarged prostate, any allergies.
Flextra DS may make you dizzy or drowsy; use caution engaging in activities requiring alertness such as driving or using machinery. Limit alcoholic beverage intake.
Acetaminophen may cause liver damage. Daily use of alcohol and acetaminophen may increase your risk for liver damage (symptoms include nausea, stomach pain, dark urine).
When Flextra DS is used in children extra caution is required. Children may be more sensitive to the effects of Flextra DS (e.g., increased excitability).
Tell your doctor if you are pregnant or intend to become pregnant before using Flextra DS. It is unknown if Flextra DS passes into breast milk. Consult your doctor before breast-feeding.
Drug Interactions
Tell your doctor of all prescription and nonprescription medication you may use, especially: other acetaminophen-containing products. Tell your doctor if you take any drugs that cause drowsiness such as: medicine for sleep (e.g., sedatives, tranquilizers), anti-anxiety drugs (e.g., diazepam, lorazepam), narcotic pain relievers (e.g., codeine, morphine), psychiatric medicines (e.g., phenothiazines such as chlorpromazine or tri cyclic antidepressants such as amitriptyline), anti-seizure drugs (e.g., carbamazepine, topiramate), muscle relaxants, certain antihistamines (e.g., diphenhydramine). Check the labels on all your medicines (e.g., cough-and-cold products) because they may contain drowsiness-causing ingredients or acetaminophen. Ask your doctor about the safe use of these products. Do not start or stop any medicine without doctor or pharmacist approval.
Flextra DS Overdose
If an overdose of Flextra DS is suspected, contact your local poison control center or emergency room immediately.
Flextra Storage
Flextra DS should be stored at room temperature between 59 and 86 degrees F (15 and 30 degrees C).
Store Flextra DS away from light and moisture.
Keep Flextra DS out of reach of children.
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Flextra DS is a prescription pain killer used to treat the minor aches and pains (e.g., headache, backache, toothache, joint pain, cramps) associated with menstrual periods, colds, flu, dental problems, or arthritis.