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CATAPRES TTS

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Catapres Tts Adverse Events Reported to the FDA Over Time

How are Catapres Tts adverse event reports trending over time?

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

Most Common Catapres Tts Adverse Events Reported to the FDA

What are the most common Catapres Tts adverse events reported to the FDA?

Blood Pressure Increased
627 (4.15%)
Drug Ineffective
469 (3.1%)
Completed Suicide
352 (2.33%)
Hypertension
347 (2.3%)
Application Site Pruritus
319 (2.11%)
Hypotension
304 (2.01%)
Application Site Erythema
302 (2%)
Dizziness
230 (1.52%)
Application Site Rash
228 (1.51%)
Headache
228 (1.51%)
Blood Pressure Inadequately Control...
223 (1.47%)
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Somnolence
193 (1.28%)
Bradycardia
134 (.89%)
Fatigue
130 (.86%)
Overdose
129 (.85%)
Application Site Irritation
125 (.83%)
Dyspnoea
123 (.81%)
Nausea
111 (.73%)
Death
110 (.73%)
Dry Mouth
109 (.72%)
Vomiting
104 (.69%)
Cardiac Arrest
100 (.66%)
Rash
100 (.66%)
Poisoning
94 (.62%)
Asthenia
93 (.62%)
Application Site Vesicles
92 (.61%)
Drug Effect Decreased
89 (.59%)
Blood Pressure Decreased
88 (.58%)
Pruritus
87 (.58%)
Chest Pain
86 (.57%)
Feeling Abnormal
85 (.56%)
Product Substitution Issue
84 (.56%)
Respiratory Arrest
84 (.56%)
Blood Pressure Fluctuation
82 (.54%)
Drug Interaction
81 (.54%)
Medication Error
78 (.52%)
Multiple Drug Overdose
78 (.52%)
Lethargy
77 (.51%)
Drug Toxicity
74 (.49%)
Loss Of Consciousness
71 (.47%)
Heart Rate Increased
70 (.46%)
Constipation
69 (.46%)
Fall
69 (.46%)
Syncope
69 (.46%)
Suicide Attempt
67 (.44%)
Pain
66 (.44%)
Product Quality Issue
64 (.42%)
Heart Rate Decreased
63 (.42%)
Anxiety
61 (.4%)
Malaise
61 (.4%)
Confusional State
60 (.4%)
Insomnia
60 (.4%)
Agitation
57 (.38%)
Hyperhidrosis
57 (.38%)
Application Site Burn
56 (.37%)
Sinus Bradycardia
56 (.37%)
Tremor
55 (.36%)
Urticaria
54 (.36%)
Convulsion
53 (.35%)
Diarrhoea
53 (.35%)
Hypersensitivity
53 (.35%)
Cardio-respiratory Arrest
51 (.34%)
Erythema
51 (.34%)
Vision Blurred
50 (.33%)
Depressed Level Of Consciousness
49 (.32%)
Cough
48 (.32%)
Hypertensive Crisis
48 (.32%)
Sedation
48 (.32%)
Palpitations
47 (.31%)
Pyrexia
47 (.31%)
Tachycardia
46 (.3%)
Cerebrovascular Accident
45 (.3%)
Delirium
44 (.29%)
Oedema Peripheral
44 (.29%)
Condition Aggravated
43 (.28%)
Drug Abuse
43 (.28%)
Gait Disturbance
43 (.28%)
Application Site Pain
41 (.27%)
Abdominal Pain
40 (.26%)
Blood Pressure Systolic Increased
39 (.26%)
Psychomotor Hyperactivity
39 (.26%)
Coma
37 (.24%)
Drug Withdrawal Syndrome
37 (.24%)
Dysarthria
37 (.24%)
Incorrect Dose Administered
36 (.24%)
Intentional Drug Misuse
36 (.24%)
Myocardial Infarction
36 (.24%)
Alopecia
35 (.23%)
Burning Sensation
35 (.23%)
Depression
35 (.23%)
Renal Failure Acute
35 (.23%)
Respiratory Depression
34 (.22%)
Accidental Overdose
33 (.22%)
Muscular Weakness
33 (.22%)
Weight Decreased
33 (.22%)
Electrocardiogram Qt Prolonged
31 (.21%)
Intentional Overdose
31 (.21%)
Pain In Extremity
31 (.21%)
Vertigo
29 (.19%)
Application Site Discolouration
28 (.19%)
Application Site Reaction
28 (.19%)

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

What are the most common Catapres Tts adverse events reported to the FDA?

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

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

Hypertension
3298
Drug Use For Unknown Indication
840
Product Used For Unknown Indication
738
Blood Pressure
312
Blood Pressure Increased
208
Attention Deficit/hyperactivity Dis...
153
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Pain
94
Hot Flush
81
Insomnia
74
Blood Pressure Abnormal
72
Sleep Disorder
67
Anxiety
58
Tourettes Disorder
52
Drug Withdrawal Syndrome
37
Cardiac Disorder
36
Blood Pressure Management
32
Ill-defined Disorder
27
Neuralgia
26
Epidural Anaesthesia
25
Agitation
25
Bipolar Disorder
24
Back Pain
23
Nerve Block
23
Abnormal Behaviour
21
Postoperative Analgesia
21
Tic
19
Psychomotor Hyperactivity
18
Menopausal Symptoms
18
Hyperhidrosis
16
Withdrawal Syndrome
15
Essential Hypertension
15
Drug Detoxification
15
Blood Pressure Fluctuation
13
Aggression
13
Depression
12
Autism
12
Spinal Anaesthesia
12
Suicide Attempt
11
Blood Pressure Systolic Increased
11
Alcohol Withdrawal Syndrome
11
Analgesic Therapy
11
Cancer Pain
11
Convulsion
10
Local Anaesthesia
10
Blood Pressure Systolic
10
Complex Regional Pain Syndrome
9
Overdose
9
Post-traumatic Stress Disorder
9
Detoxification
9
Drug Exposure During Pregnancy
8
Anaesthesia
8

Drug Labels

LabelLabelerEffective
CatapresPhysicians Total Care, Inc.10-MAY-10
CatapresRebel Distributors Corp10-DEC-10
CatapresBoehringer Ingelheim Pharmaceuticals Inc.15-JUN-12

Catapres Tts Case Reports

What Catapres Tts 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 Catapres Tts. 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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