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CitraNatal Assure
is a prescription prenatal/postnatal multivitamin/mineral tablet
with Ferr-Ease
, a patented dual-iron delivery
comprising both a quick release and slow release iron, and a capsule
of an essential fatty acid. The prenatal vitamin is a white, coated,
oval multivitamin/mineral tablet. The tablet is debossed "0891" on
one side and is blank on the other. The essential fatty acid DHA capsule
is caramel colored and contains a light yellow to orange semi-solid
mixture.
Other ingredients in DHA
gelatin capsule: Gelatin, sunflower oil, glycerin, caramel color,
sunflower lecithin, rosemary extract, tocopherols, ascorbyl palmitate.
What does CitraNatal Assure look like?
What are the available doses of CitraNatal Assure?
Sorry No records found.
What should I talk to my health care provider before I take CitraNatal Assure?
Sorry No records found
How should I use CitraNatal Assure?
CitraNatal Assure
is a multivitamin/mineral prescription drug indicated
for use in improving the nutritional status of women prior to conception,
throughout pregnancy, and in the postnatal period for both lactating
and nonlactating mothers.
One tablet and one capsule daily or as directed
by a physician.
What interacts with CitraNatal Assure?
This product is contraindicated in patients
with a known hypersensitivity to any of the ingredients.
What are the warnings of CitraNatal Assure?
Sorry No Records found
What are the precautions of CitraNatal Assure?
Folic acid in doses above 0.1
mg daily may obscure pernicious anemia in that hematologic remission
can occur while neurological manifestations progress.
What are the side effects of CitraNatal Assure?
Allergic sensitization has been reported following
both oral and parenteral administration of folic acid.
What should I look out for while using CitraNatal Assure?
This product is contraindicated in patients
with a known hypersensitivity to any of the ingredients.
Folic acid alone is improper therapy
in the treatment of pernicious anemia and other megaloblastic anemias
where vitamin B
is deficient.
What might happen if I take too much CitraNatal Assure?
Sorry No Records found
How should I store and handle CitraNatal Assure?
StorageSix child-resistant blister packs of 5 tablets and 5 capsules each - NDC 0178-0891-30
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Clinical Information
Chemical Structure
No Image found
Clinical Pharmacology
Non-Clinical Toxicology
This product is contraindicated in patients
with a known hypersensitivity to any of the ingredients.
Folic acid alone is improper therapy
in the treatment of pernicious anemia and other megaloblastic anemias
where vitamin B
is deficient.
Bleeding has been reported in patients treated with pentoxifylline with or without concomitant NSAIDs, anticoagulants, or platelet aggregation inhibitors.
Increased prothrombin time has been reported in patients concomitantly treated with pentoxifylline and vitamin K antagonists. Monitoring of anticoagulant activity in these patients is recommended when pentoxifylline is introduced or the dose is changed.
Concomitant administration of pentoxifylline and theophylline-containing drugs leads to increased theophylline levels and theophylline toxicity in some individuals. Monitor theophylline levels when starting pentoxifylline or changing dose.
Concomitant administration of strong CYP1A2 inhibitors (including e.g. ciprofloxacin or fluvoxamine) may increase the exposure to pentoxifylline (see ).
Pentoxifylline has been used concurrently with antihypertensive drugs, beta blockers, digitalis, diuretics, and antiarrhythmics, without observed problems. Small decreases in blood pressure have been observed in some patients treated with pentoxifylline plus nifedipine or captopril; periodic systemic blood pressure monitoring is recommended for patients receiving concomitant antihypertensive therapy. If indicated, dosage of the antihypertensive agents should be reduced.
Postmarketing cases of increased anticoagulant activity have been reported in patients concomitantly treated with pentoxifylline and vitamin K antagonists. Monitoring of anticoagulant activity in these patients is recommended when pentoxifylline is introduced or the dose is changed.
Concomitant administration with cimetidine is reported to increase the average steady state plasma concentration of pentoxifylline (~25%) and the Metabolite I (~30%).
Folic acid in doses above 0.1
mg daily may obscure pernicious anemia in that hematologic remission
can occur while neurological manifestations progress.
Allergic sensitization has been reported following
both oral and parenteral administration of folic acid.
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Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
Clonazepam Description
Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake.
Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula:
C15H10ClN3O3 M.W. 315.72
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Tips
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Interactions
Interactions
A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib).
228 major drug interactions (854 brand and generic names)
210 moderate drug interactions (691 brand and generic names)
2 minor drug interactions (4 brand and generic names)
Show all medications in the database that may interact with Imbruvica (ibrutinib).
