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Soma Adverse Events Reported to the FDA Over Time

How are Soma adverse event reports trending over time?

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

Most Common Soma Adverse Events Reported to the FDA

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

Completed Suicide
459 (2.04%)
Overdose
343 (1.52%)
Vomiting
342 (1.52%)
Drug Hypersensitivity
314 (1.4%)
Drug Toxicity
301 (1.34%)
Nausea
257 (1.14%)
Drug Interaction
230 (1.02%)
Somnolence
226 (1%)
Dyspnoea
220 (.98%)
Multiple Drug Overdose
206 (.92%)
Headache
188 (.84%)
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Loss Of Consciousness
188 (.84%)
Malaise
180 (.8%)
Drug Ineffective
174 (.77%)
Death
164 (.73%)
Abdominal Pain
162 (.72%)
Cardiac Arrest
162 (.72%)
Drug Abuse
162 (.72%)
Dizziness
160 (.71%)
Pain
158 (.7%)
Constipation
152 (.68%)
Respiratory Arrest
152 (.68%)
Confusional State
146 (.65%)
Pyrexia
145 (.64%)
Multiple Drug Overdose Intentional
143 (.64%)
Back Pain
140 (.62%)
Depression
123 (.55%)
Fatigue
123 (.55%)
Hypotension
123 (.55%)
Suicide Attempt
119 (.53%)
Cardio-respiratory Arrest
115 (.51%)
Fall
115 (.51%)
Intentional Overdose
111 (.49%)
Convulsion
109 (.48%)
Hallucination
107 (.48%)
Drug Exposure During Pregnancy
105 (.47%)
Asthenia
103 (.46%)
Intentional Drug Misuse
103 (.46%)
Diarrhoea
102 (.45%)
Accidental Overdose
97 (.43%)
Drug Dependence
95 (.42%)
Alanine Aminotransferase Increased
94 (.42%)
Serotonin Syndrome
94 (.42%)
Tremor
93 (.41%)
Insomnia
92 (.41%)
Rash
91 (.4%)
Feeling Abnormal
90 (.4%)
Pruritus
86 (.38%)
Agitation
85 (.38%)
Cough
85 (.38%)
Respiratory Depression
85 (.38%)
Depressed Level Of Consciousness
84 (.37%)
Weight Increased
84 (.37%)
Hyperhidrosis
82 (.36%)
Anxiety
81 (.36%)
Hypertension
81 (.36%)
Medication Error
81 (.36%)
Hypersensitivity
77 (.34%)
Coma
76 (.34%)
Metabolic Acidosis
76 (.34%)
Dehydration
75 (.33%)
Poisoning
75 (.33%)
Arthralgia
70 (.31%)
Muscle Spasms
70 (.31%)
Pneumonia
70 (.31%)
Renal Failure
69 (.31%)
Suicidal Ideation
68 (.3%)
Unresponsive To Stimuli
68 (.3%)
Chest Pain
66 (.29%)
Abdominal Pain Upper
65 (.29%)
Pulmonary Oedema
65 (.29%)
Lethargy
64 (.28%)
Renal Failure Acute
63 (.28%)
Tachycardia
63 (.28%)
Aspartate Aminotransferase Increase...
62 (.28%)
Condition Aggravated
62 (.28%)
Heart Rate Increased
62 (.28%)
Substance Abuse
62 (.28%)
Decreased Appetite
60 (.27%)
Oedema Peripheral
60 (.27%)
Drug Abuser
59 (.26%)
Pain In Extremity
59 (.26%)
Cerebrovascular Accident
58 (.26%)
Mental Status Changes
58 (.26%)
Weight Decreased
58 (.26%)
Atrial Fibrillation
57 (.25%)
Hypoaesthesia
57 (.25%)
Hypoxia
57 (.25%)
Amnesia
56 (.25%)
Blood Creatinine Increased
54 (.24%)
Road Traffic Accident
53 (.24%)
Syncope
53 (.24%)
International Normalised Ratio Incr...
52 (.23%)
Musculoskeletal Stiffness
51 (.23%)
Urticaria
51 (.23%)
Myalgia
49 (.22%)
Urinary Retention
49 (.22%)
Drug Withdrawal Syndrome
48 (.21%)
Jaundice
48 (.21%)
Paraesthesia
48 (.21%)
Abdominal Distension
47 (.21%)

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

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

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

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

Pain
2345
Drug Use For Unknown Indication
1968
Product Used For Unknown Indication
1445
Cough
674
Back Pain
620
Muscle Spasms
447
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Muscle Relaxant Therapy
269
Migraine
218
Rheumatoid Arthritis
207
Arthralgia
196
Headache
187
Analgesic Therapy
169
Osteoarthritis
126
Fibromyalgia
121
Arthritis
115
Diarrhoea
112
Ill-defined Disorder
88
Musculoskeletal Pain
83
Pain In Extremity
70
Abdominal Pain
64
Neck Pain
62
Myalgia
58
Bronchitis
56
Procedural Pain
54
Cancer Pain
48
Analgesia
46
Sciatica
43
Back Disorder
43
Insomnia
43
Sleep Disorder
43
Suicide Attempt
41
Drug Exposure During Pregnancy
41
Pain Management
40
Toothache
38
Crohns Disease
35
Bone Pain
35
Analgesic Effect
34
Foetal Exposure During Pregnancy
34
Neuralgia
33
Upper Respiratory Tract Infection
33
Breakthrough Pain
32
Chest Pain
30
Antitussive Therapy
28
Nasopharyngitis
24
Symphysiolysis
24
Pharyngitis Streptococcal
23
Muscle Disorder
22
Anxiety
21
Ankylosing Spondylitis
21
Pyrexia
19
Pneumonia
19

Drug Labels

LabelLabelerEffective
SomaRebel Distributors Corp01-DEC-10
SomaSTAT RX USA LLC07-JUL-11
SomaLake Erie Medical & Surgical Supply DBA Quality Care Products LLC31-MAY-12
SomaMeda Pharmaceuticals Inc.31-JAN-13
Soma Anti-cancergenSOMA Biotechnology Co., Ltd22-APR-13
Soma HyulgihwanSOMA Biotechnology Co., Ltd29-APR-13
Soma Pet-circleSOMA Biotechnology Co., Ltd02-MAY-13
Soma DisordergenSOMA Biotechnology Co., Ltd02-MAY-13
Soma ArthritSOMA Biotechnology Co., Ltd06-MAY-13
Soma AtocellSOMA Biotechnology Co., Ltd06-MAY-13
Soma HepatiSOMA Biotechnology Co., Ltd06-MAY-13
Soma CircumSOMA Biotechnology Co., Ltd06-MAY-13
Soma CroimSOMA Biotechnology Co., Ltd06-MAY-13
Soma Heart-qSOMA Biotechnology Co., Ltd06-MAY-13
Soma ProuriSOMA Biotechnology Co., Ltd06-MAY-13
Soma Diat SOMA Biotechnology Co., Ltd06-MAY-13

Soma Case Reports

What Soma 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 Soma. 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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