Ascor L 500 Side Effects
Generic Name: ascorbic acid
Note: This page contains information about the side effects of ascorbic acid. Some of the dosage forms included on this document may not apply to the brand name Ascor L 500.
Not all side effects for Ascor L 500 may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here.
For the Consumer
Applies to ascorbic acid: oral capsule, oral capsule extended release, oral capsule liquid filled, oral granule, oral liquid, oral lozenge/troche, oral powder, oral powder for solution, oral powder for suspension, oral solution, oral syrup, oral tablet, oral tablet chewable, oral tablet extended release, oral wafer
In addition to its needed effects, some unwanted effects may be caused by ascorbic acid (the active ingredient contained in Ascor L 500). In the event that any of these side effects do occur, they may require medical attention.
If any of the following side effects occur while taking ascorbic acid, check with your doctor or nurse as soon as possible:Less common or rare - with high doses
- Side or lower back pain
Some of the side effects that can occur with ascorbic acid may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:Less common or rare - with high doses
- dizziness or faintness (with the injection only)
- flushing or redness of skin
- increase in urination (mild)
- nausea or vomiting
- stomach cramps
For Healthcare Professionals
Applies to ascorbic acid: compounding powder, injectable solution, oral capsule, oral gum, oral liquid, oral tablet, oral tablet chewable, oral tablet disintegrating, oral tablet extended release
Renal side effects have included oxalate and urate kidney stones.
Hyperoxaluria appears to be dose-related.
Migraine headache has been reported with a daily dose of 6 grams.
The manufacturer reports temporary dizziness and faintness may be associated with too rapid of a rate during intravenous administration.
Nervous system side effects have included dizziness, faintness, fatigue, and headache in less than 1% of patients. Migraine headache has also been reported.
Other side effects have included flank pain in less than 1% of patients. Conditional scurvy has also been reported.
Conditional scurvy is reported to occur following excessive doses of ascorbic acid over a prolonged period of time. The mechanism of action for this condition is thought to be that large doses of ascorbic acid condition the patient over time for rapid clearance of ascorbic acid resulting in scurvy. The plasma levels of ascorbic acid appear to remain within normal limits. The actual existence of conditional scurvy remains controversial.
Nausea, diarrhea, and abdominal cramps appears to be associated with doses exceeding 2 g per day, although there have been some reports with as little as 1 g per day.
Esophagitis appears to be associated with prolonged or increased contact of ascorbic acid (the active ingredient contained in Ascor L 500) tablets with the esophageal mucosa.
Gastrointestinal side effects have included nausea, diarrhea, abdominal cramps, and esophagitis.
Hematologic side effects have included hemolysis.
The majority of hemolysis reports have been associated with patients who have concurrent glucose-6-phosphate dehydrogenase deficiency.
Local side effects have included transient mild soreness at the site of injection.
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