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MECLIZINE

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Meclizine Adverse Events Reported to the FDA Over Time

How are Meclizine adverse event reports trending over time?

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

Most Common Meclizine Adverse Events Reported to the FDA

What are the most common Meclizine adverse events reported to the FDA?

Drug Ineffective
127 (7.29%)
Dizziness
93 (5.34%)
Completed Suicide
36 (2.07%)
Nausea
27 (1.55%)
Somnolence
26 (1.49%)
Hypersensitivity
24 (1.38%)
Headache
23 (1.32%)
Malaise
23 (1.32%)
Vertigo
20 (1.15%)
Drug Hypersensitivity
19 (1.09%)
Drug Exposure During Pregnancy
17 (.98%)
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Fatigue
17 (.98%)
Depression
15 (.86%)
Drug Toxicity
15 (.86%)
Fall
15 (.86%)
Feeling Abnormal
15 (.86%)
Asthenia
14 (.8%)
Dysarthria
14 (.8%)
Asthma
13 (.75%)
Hyperhidrosis
13 (.75%)
Hypotension
13 (.75%)
Respiratory Arrest
12 (.69%)
Diabetes Mellitus
11 (.63%)
Drug Interaction
11 (.63%)
Dyspnoea
11 (.63%)
Hypertension
11 (.63%)
Vision Blurred
11 (.63%)
Balance Disorder
10 (.57%)
Cardiac Arrest
10 (.57%)
Muscle Twitching
10 (.57%)
Amnesia
9 (.52%)
Anaemia
9 (.52%)
Anxiety
9 (.52%)
Cardio-respiratory Arrest
9 (.52%)
Confusional State
9 (.52%)
Death
9 (.52%)
Hallucination
9 (.52%)
Overdose
9 (.52%)
Syncope
9 (.52%)
Convulsion
8 (.46%)
Diarrhoea
8 (.46%)
Loss Of Consciousness
8 (.46%)
Vomiting
8 (.46%)
Abdominal Discomfort
7 (.4%)
Condition Aggravated
7 (.4%)
Diplopia
7 (.4%)
Drug Effect Decreased
7 (.4%)
Gait Disturbance
7 (.4%)
Incorrect Dose Administered
7 (.4%)
Medication Error
7 (.4%)
Memory Impairment
7 (.4%)
Palpitations
7 (.4%)
Prostate Cancer
7 (.4%)
Psychotic Disorder
7 (.4%)
Tremor
7 (.4%)
Weight Decreased
7 (.4%)
Blood Cholesterol Abnormal
6 (.34%)
Blood Glucose Decreased
6 (.34%)
Blood Pressure Fluctuation
6 (.34%)
Body Height Decreased
6 (.34%)
Coronary Artery Bypass
6 (.34%)
Gastrooesophageal Reflux Disease
6 (.34%)
Hallucination, Visual
6 (.34%)
Hot Flush
6 (.34%)
Influenza Like Illness
6 (.34%)
Product Substitution Issue
6 (.34%)
Rash
6 (.34%)
Spinal Column Stenosis
6 (.34%)
Weight Increased
6 (.34%)
Activities Of Daily Living Impaired
5 (.29%)
Alcohol Use
5 (.29%)
Blood Pressure Increased
5 (.29%)
Cardiac Disorder
5 (.29%)
Coma
5 (.29%)
Dehydration
5 (.29%)
Dyskinesia
5 (.29%)
Erectile Dysfunction
5 (.29%)
Eye Disorder
5 (.29%)
Eyelid Ptosis
5 (.29%)
Fluid Retention
5 (.29%)
Insomnia
5 (.29%)
Nervousness
5 (.29%)
Oedema Peripheral
5 (.29%)
Orthostatic Hypotension
5 (.29%)
Pain In Extremity
5 (.29%)
Pelvic Fracture
5 (.29%)
Strabismus
5 (.29%)
Tinnitus
5 (.29%)
Alopecia
4 (.23%)
Angioplasty
4 (.23%)
Arthralgia
4 (.23%)
Bladder Neoplasm
4 (.23%)
Blood Cholesterol Increased
4 (.23%)
Blood Testosterone Decreased
4 (.23%)
Central Nervous System Lesion
4 (.23%)
Chest Discomfort
4 (.23%)
Clavicle Fracture
4 (.23%)
Cleft Palate
4 (.23%)
Cough
4 (.23%)
Cyst
4 (.23%)
Cystic Lymphangioma
4 (.23%)

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

What are the most common Meclizine adverse events reported to the FDA?

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

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

Dizziness
493
Vertigo
397
Drug Use For Unknown Indication
168
Product Used For Unknown Indication
141
Nausea
79
Menieres Disease
40
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Motion Sickness
33
Balance Disorder
24
Vomiting
18
Inner Ear Disorder
15
Akathisia
8
Prophylaxis Of Nausea And Vomiting
8
Headache
7
Ill-defined Disorder
7
Tinnitus
6
Prophylaxis
5
Drug Exposure During Pregnancy
5
Vertigo Positional
5
Labyrinthitis
5
Hypertension
4
Sinusitis
4
Ear Disorder
4
Antiallergic Therapy
4
Muscle Relaxant Therapy
4
Migraine
4
Pain
3
Drug Therapy
3
Hypersensitivity
3
Multiple Sclerosis
3
Neuritis
3
Head Injury
3
Antiemetic Supportive Care
2
Suicide Attempt
2
Mallory-weiss Syndrome
2
Autoimmune Disorder
2
Gastrooesophageal Reflux Disease
2
Intentional Overdose
2
Cerebrovascular Accident
2
Pneumonia
2
Diabetes Mellitus
2
Brain Injury
2
Acoustic Neuroma
2
Hallucination
2
Otitis Media
1
Rheumatoid Arthritis
1
Sinus Disorder
1
Transient Ischaemic Attack
1
Traumatic Brain Injury
1
Subclavian Steal Syndrome
1
Hyperthyroidism
1
Overdose
1

Drug Labels

LabelLabelerEffective
BonineInsight Pharmaceuticals11-JAN-10
Meclizine HydrochlorideUDL Laboratories, Inc.12-MAR-10
Meclizine HydrochlorideState of Florida DOH Central Pharmacy26-MAY-10
Meclizine Hydrochloride Blenheim Pharmacal, Inc.10-SEP-10
Meclizine HydrochlorideRebel Distributors Corp.15-SEP-10
Meclizine HydrochloridePhysicians Total Care, Inc.15-SEP-10
Medique Medi-meclizineUnifirst First Aid Corporation20-SEP-10
Meclizine Hydrochloride JUBILANT CADISTA PHARMACEUTICALS, INC.04-MAR-11
Meclizine HydrochlorideMylan Pharmaceuticals Inc.17-MAR-11
Meclizine HydrochlorideCardinal Health17-MAY-11
Meclizine Hydrochloride Par Pharmaceutical, Inc.14-JUN-11
Meclizine HydrochlorideUnit Dose Services14-JUN-11
AntivertRoerig06-JUL-11
Meclizine HydrochlorideAmerican Health Packaging12-JUL-11
MeclizineContract Pharmacal Corp26-DEC-11
MeclizineContract Pharmacal Corp26-DEC-11
Meclizine HydrochlorideGolden State Medical Supply, Inc.09-JAN-12
Meclizine HydrochlorideMcKesson Contract Packaging11-JAN-12
Meclizine Hydrochloride H.J. Harkins Company, Inc.19-JAN-12
Meclizine HydrochlorideLake Erie Medical & Surgical Supply DBA Quality Care Products LLC23-JAN-12
Meclizine Hydrochloride H.J. Harkins Company, Inc.16-FEB-12
Meclizine HydrochlorideLife Line Home Care Services, Inc.20-FEB-12
Meclizine HydrochlorideSandoz Inc10-APR-12
Meclizine HydrochlorideAmneal Pharmaceuticals11-APR-12
Meclizine HydrochlorideCardinal Health03-MAY-12
Meclizine Hydrochloride AvKARE, Inc.04-MAY-12
Meclizine HydrochlorideEpic Pharma, LLC13-AUG-12
Meclizine Hydrochloride STAT Rx USA LLC20-SEP-12
Meclizine HydrochlorideNCS HealthCare of KY, Inc dba Vangard Labs02-NOV-12
Meclizine HclRugby Laboratories Inc.09-DEC-12
Meclizine HclRugby Laboratories Inc.09-DEC-12
Meclizine HclPreferred Pharmaceuticals, Inc.13-DEC-12
Meclizine HclPreferred Pharmaceuticals, Inc.13-DEC-12
Meclizine HclBryant Ranch Prepack13-FEB-13
Meclizine HclBryant Ranch Prepack13-FEB-13
Naus-easeSunascen Therapeutics LLC03-MAR-13
Meclizine Hydrochloride Bryant Ranch Prepack06-MAR-13
Meclizine Hydrochloride AvKARE, Inc.25-APR-13

Meclizine Case Reports

What Meclizine 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 Meclizine. 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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