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ASCORBIC ACID

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Ascorbic Acid Adverse Events Reported to the FDA Over Time

How are Ascorbic Acid adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Ascorbic Acid, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Ascorbic Acid is flagged as the suspect drug causing the adverse event.

Most Common Ascorbic Acid Adverse Events Reported to the FDA

What are the most common Ascorbic Acid adverse events reported to the FDA?

Nausea
32 (1.48%)
Vomiting
29 (1.34%)
Drug Interaction
27 (1.25%)
Dyspnoea
26 (1.2%)
Fatigue
25 (1.16%)
Pyrexia
25 (1.16%)
Diarrhoea
23 (1.06%)
Asthenia
21 (.97%)
Dehydration
19 (.88%)
Renal Failure Acute
18 (.83%)
Anaemia
17 (.79%)
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Condition Aggravated
17 (.79%)
Confusional State
16 (.74%)
Disease Progression
16 (.74%)
Hypotension
16 (.74%)
Toxic Epidermal Necrolysis
16 (.74%)
Abdominal Pain
15 (.69%)
Drug Exposure During Pregnancy
15 (.69%)
Malaise
15 (.69%)
Pneumonia
15 (.69%)
Back Pain
13 (.6%)
Cerebral Haemorrhage
13 (.6%)
Pleural Effusion
13 (.6%)
Dizziness
12 (.55%)
Sepsis
12 (.55%)
Somnolence
12 (.55%)
Anorexia
11 (.51%)
Convulsion
11 (.51%)
Malignant Neoplasm Progression
11 (.51%)
Renal Failure
11 (.51%)
Acute Hepatic Failure
10 (.46%)
Arthralgia
10 (.46%)
Aspartate Aminotransferase Increase...
10 (.46%)
Multiple Myeloma
10 (.46%)
Oedema
10 (.46%)
Thrombocytopenia
10 (.46%)
Atrial Fibrillation
9 (.42%)
Constipation
9 (.42%)
Insomnia
9 (.42%)
Jaundice
9 (.42%)
Muscular Weakness
9 (.42%)
Pain
9 (.42%)
Rash
9 (.42%)
Alanine Aminotransferase Increased
8 (.37%)
Blood Pressure Increased
8 (.37%)
Chills
8 (.37%)
Haemoglobin Decreased
8 (.37%)
Hepatic Necrosis
8 (.37%)
Hypercalcaemia
8 (.37%)
Lethargy
8 (.37%)
Liver Disorder
8 (.37%)
Pancytopenia
8 (.37%)
Pericardial Effusion
8 (.37%)
Pulmonary Haemorrhage
8 (.37%)
Septic Shock
8 (.37%)
Tachycardia
8 (.37%)
Abdominal Distension
7 (.32%)
Convulsive Threshold Lowered
7 (.32%)
Decreased Appetite
7 (.32%)
Dyspepsia
7 (.32%)
Electrocardiogram Qt Prolonged
7 (.32%)
Fall
7 (.32%)
Foetal Growth Retardation
7 (.32%)
Haematemesis
7 (.32%)
Headache
7 (.32%)
Hyperglycaemia
7 (.32%)
Stomatitis
7 (.32%)
Tremor
7 (.32%)
Urinary Tract Infection
7 (.32%)
Agitation
6 (.28%)
Aphthous Stomatitis
6 (.28%)
Ascites
6 (.28%)
Body Temperature Increased
6 (.28%)
Cardiac Disorder
6 (.28%)
Cataract
6 (.28%)
Chest Pain
6 (.28%)
Cough
6 (.28%)
Death
6 (.28%)
Drug Ineffective
6 (.28%)
Erythema
6 (.28%)
Flushing
6 (.28%)
General Physical Health Deteriorati...
6 (.28%)
Hyperkalaemia
6 (.28%)
Hypoaesthesia
6 (.28%)
Incorrect Dose Administered
6 (.28%)
Melaena
6 (.28%)
Mental Status Changes
6 (.28%)
Oral Herpes
6 (.28%)
Placental Infarction
6 (.28%)
Prothrombin Time Prolonged
6 (.28%)
Pruritus
6 (.28%)
Pulmonary Oedema
6 (.28%)
Respiratory Failure
6 (.28%)
Ulcerative Keratitis
6 (.28%)
Vision Blurred
6 (.28%)
Abdominal Pain Upper
5 (.23%)
Acute Respiratory Distress Syndrome
5 (.23%)
Anxiety
5 (.23%)
Blood Bilirubin Increased
5 (.23%)
Blood Iron Increased
5 (.23%)
Blood Sodium Decreased
5 (.23%)

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This graph shows the top adverse events submitted to the FDA for Ascorbic Acid, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Ascorbic Acid is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Ascorbic Acid

What are the most common Ascorbic Acid adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Ascorbic Acid, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Ascorbic Acid is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Ascorbic Acid According to Those Reporting Adverse Events

Why are people taking Ascorbic Acid, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
942
Drug Use For Unknown Indication
886
Vitamin Supplementation
543
Supplementation Therapy
202
Medical Diet
129
Routine Health Maintenance
110
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Prophylaxis
107
Nutritional Support
53
Multiple Myeloma
39
Anaemia
31
General Physical Condition
26
Acute Myeloid Leukaemia
24
Nasopharyngitis
24
Myelodysplastic Syndrome
23
Vitamin C Deficiency
17
Metastatic Malignant Melanoma
13
Ill-defined Disorder
12
Immune System Disorder
12
Mineral Supplementation
12
Asthenia
12
Hypovitaminosis
11
Pharyngitis
10
Vitamin C
10
Crohns Disease
9
Iron Deficiency
9
Multiple Sclerosis
8
Alcohol Withdrawal Syndrome
7
Unevaluable Event
7
Influenza
6
Pancreatic Carcinoma Metastatic
6
Immune Enhancement Therapy
6
Postoperative Care
6
Small Cell Lung Cancer Metastatic
6
Iron Deficiency Anaemia
5
Food Allergy
5
Feeling Cold
5
Hypertension
5
Adverse Event
5
Rheumatoid Arthritis
4
Blood Iron Decreased
4
Pigmentation Disorder
4
Fatigue
4
Melaena
4
Arthralgia
4
Albuminuria
4
Vomiting
4
Infection
4
Malaise
4
Cystic Fibrosis
4
Diarrhoea
4
Thyroid Disorder
4

Drug Labels

LabelLabelerEffective
Ascorbic AcidBioniche Pharma USA LLC12-FEB-10
Ascorbic AcidThe Torrance Company12-MAR-13
MoviprepSalix Pharmaceuticals, Inc.20-MAR-13

Ascorbic Acid Case Reports

What Ascorbic Acid safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Ascorbic Acid. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

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