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MULTI VITAMINS

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Multi Vitamins Adverse Events Reported to the FDA Over Time

How are Multi Vitamins adverse event reports trending over time?

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

Most Common Multi Vitamins Adverse Events Reported to the FDA

What are the most common Multi Vitamins adverse events reported to the FDA?

Cleft Palate
25 (2.6%)
Memory Impairment
17 (1.77%)
Choking
13 (1.35%)
Drug Interaction
13 (1.35%)
Nausea
13 (1.35%)
Cardiac Disorder
11 (1.15%)
Cleft Lip
11 (1.15%)
Malaise
11 (1.15%)
Eustachian Tube Dysfunction
10 (1.04%)
Medication Error
10 (1.04%)
Otitis Media Chronic
10 (1.04%)
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Respiratory Disorder
10 (1.04%)
Arthralgia
9 (.94%)
Body Dysmorphic Disorder
9 (.94%)
Craniosynostosis
9 (.94%)
Deafness
9 (.94%)
Developmental Delay
9 (.94%)
Emotional Disorder
9 (.94%)
Flushing
9 (.94%)
Glaucoma
9 (.94%)
Headache
9 (.94%)
Hyperbilirubinaemia
9 (.94%)
Pierre Robin Syndrome
9 (.94%)
Congenital Anomaly
8 (.83%)
Myocardial Infarction
8 (.83%)
Weight Decreased
8 (.83%)
Dyspepsia
7 (.73%)
Maternal Drugs Affecting Foetus
7 (.73%)
Vomiting
7 (.73%)
Bradycardia
6 (.63%)
Condition Aggravated
6 (.63%)
Dehydration
6 (.63%)
Diarrhoea
6 (.63%)
Dyspnoea
6 (.63%)
Ear Infection
6 (.63%)
Feeling Abnormal
6 (.63%)
Gastrooesophageal Reflux Disease
6 (.63%)
Hydrocele
6 (.63%)
Jaundice Neonatal
6 (.63%)
Caesarean Section
5 (.52%)
Cerebrovascular Accident
5 (.52%)
Completed Suicide
5 (.52%)
Conductive Deafness
5 (.52%)
Constipation
5 (.52%)
Drug Exposure During Pregnancy
5 (.52%)
Fatigue
5 (.52%)
Feeding Disorder
5 (.52%)
Hyperhidrosis
5 (.52%)
Hypersensitivity
5 (.52%)
Speech Disorder
5 (.52%)
Tremor
5 (.52%)
Abdominal Discomfort
4 (.42%)
Aneurysm
4 (.42%)
Arterial Disorder
4 (.42%)
Blood Glucose Increased
4 (.42%)
Bronchial Hyperreactivity
4 (.42%)
Cardio-respiratory Arrest
4 (.42%)
Confusional State
4 (.42%)
Cyanosis
4 (.42%)
Diabetes Mellitus
4 (.42%)
Dizziness
4 (.42%)
Drug Ineffective
4 (.42%)
Gestational Diabetes
4 (.42%)
Hypertension
4 (.42%)
Nasopharyngitis
4 (.42%)
Pain In Extremity
4 (.42%)
Pneumonia
4 (.42%)
Pneumonia Aspiration
4 (.42%)
Pregnancy
4 (.42%)
Premature Baby
4 (.42%)
Pruritus
4 (.42%)
Respiratory Arrest
4 (.42%)
Subarachnoid Haemorrhage
4 (.42%)
Upper Respiratory Tract Infection
4 (.42%)
Uterine Contractions During Pregnan...
4 (.42%)
Abdominal Pain Upper
3 (.31%)
Agitation
3 (.31%)
Anaemia
3 (.31%)
Anxiety
3 (.31%)
Asthenia
3 (.31%)
Blood Pressure Decreased
3 (.31%)
Bronchitis
3 (.31%)
Bronchomalacia
3 (.31%)
Burns Second Degree
3 (.31%)
Chills
3 (.31%)
Decreased Appetite
3 (.31%)
Depression
3 (.31%)
Diabetic Neuropathy
3 (.31%)
Drug Withdrawal Syndrome Neonatal
3 (.31%)
Dry Mouth
3 (.31%)
Erythema
3 (.31%)
Faeces Discoloured
3 (.31%)
Fibromyalgia
3 (.31%)
Foetal Distress Syndrome
3 (.31%)
Heart Rate Decreased
3 (.31%)
Hypotension
3 (.31%)
Loss Of Consciousness
3 (.31%)
Muscle Spasms
3 (.31%)
Musculoskeletal Stiffness
3 (.31%)
Neuropathy Peripheral
3 (.31%)
No Adverse Event
3 (.31%)

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This graph shows the top adverse events submitted to the FDA for Multi Vitamins, 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 Multi Vitamins 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 Multi Vitamins

What are the most common Multi Vitamins adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Multi Vitamins, 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 Multi Vitamins 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 Multi Vitamins According to Those Reporting Adverse Events

Why are people taking Multi Vitamins, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
1120
Drug Use For Unknown Indication
868
Vitamin Supplementation
678
Supplementation Therapy
332
Medical Diet
227
Nutritional Support
122
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Pregnancy
122
Routine Health Maintenance
115
Prophylaxis
82
Foetal Exposure During Pregnancy
56
General Physical Condition
29
Anaemia
15
Crohns Disease
13
Hypovitaminosis
12
Malnutrition
11
Ill-defined Disorder
11
Hiv Infection
9
Drug Exposure During Pregnancy
8
Hyperemesis Gravidarum
7
Eye Disorder
7
Fatigue
7
Immune System Disorder
7
Prenatal Care
6
Macular Degeneration
6
Rheumatoid Arthritis
5
Mineral Supplementation
5
Malabsorption
4
Obesity Surgery
4
Bone Disorder
4
Osteopenia
4
Asthenia
4
Unevaluable Event
4
Inflammatory Bowel Disease
4
Cystic Fibrosis
4
Mitral Valve Prolapse
4
Supportive Care
3
Depression
3
Alcoholism
3
Hepatitis B Virus Test
3
Renal Tubular Disorder
3
Blood Pressure
3
Dehydration
3
Blood Cholesterol
3
Alcohol Use
3
Liver Disorder
3
Optic Nerve Disorder
2
Hypertensive Crisis
2
Cardiac Disorder
2
Glossodynia
2
Aphthous Stomatitis
2
Pre-existing Condition Improved
2

Multi Vitamins Case Reports

What Multi Vitamins 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 Multi Vitamins. 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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