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Clonidine Transdermal System Side Effects

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Common Clonidine Transdermal System Side Effects



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If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Clonidine Transdermal System Side Effects Reported to FDA



Clonidine Transdermal System Side Effect Report#9995978
Pruritus, Erythema, Scab, Hypertension, Headache, Dry Skin
This is a report of a 66-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: hypertension, who was treated with Clonidine Transdermal System (dosage: NA, start time: 201207), combined with: NA. and developed a serious reaction and side effect(s): Pruritus, Erythema, Scab, Hypertension, Headache, Dry Skin after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System treatment in female patients, resulting in Pruritus side effect.
Clonidine Transdermal System Side Effect Report#9513560
Blood Pressure Systolic Increased, Hypertension, Feeling Jittery, Tremor, Heart Rate Increased, Burning Sensation
This report suggests a potential Clonidine Transdermal System Blood Pressure Systolic Increased side effect(s) that can have serious consequences. A 51-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: blood pressure increased,hypertension and used Clonidine Transdermal System (dosage: Change Patch Every Week) starting 2013. After starting Clonidine Transdermal System the patient began experiencing various side effects, including: Blood Pressure Systolic Increased, Hypertension, Feeling Jittery, Tremor, Heart Rate Increased, Burning SensationAdditional drugs used concurrently: NA. Although Clonidine Transdermal System demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Systolic Increased, may still occur.
Clonidine Transdermal System Side Effect Report#9417435
Blood Pressure Increased, Hot Flush
This Blood Pressure Increased problem was reported by a consumer or non-health professional from US. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: blood pressure increased,hot flush. On NS this consumer started treatment with Clonidine Transdermal System Usp (dosage: Changed Qweek). The following drugs were being taken at the same time: NA. When using Clonidine Transdermal System Usp, the patient experienced the following unwanted symptoms/side effects: Blood Pressure Increased, Hot FlushAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Pressure Increased, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9417434
Application Site Pruritus, Application Site Erythema
This Application Site Pruritus side effect was reported by a consumer or non-health professional from US. A 70-year-old male patient (weight:NA) experienced the following symptoms/conditions: blood pressure increased.The patient was prescribed Clonidine Transdermal System Usp (drug dosage: NA), which was initiated on 201209. Concurrently used drugs: NA..After starting to take Clonidine Transdermal System Usp the consumer reported adverse symptoms, such as: Application Site Pruritus, Application Site ErythemaThese side effects may potentially be related to Clonidine Transdermal System Usp.
Clonidine Transdermal System Side Effect Report#9417431
Blood Pressure Increased
This is a report of a 69-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: blood pressure increased, who was treated with Clonidine Transdermal System Usp (dosage: Qw, start time:
May 17, 2013), combined with: NA. and developed a serious reaction and side effect(s): Blood Pressure Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System Usp treatment in female patients, resulting in Blood Pressure Increased side effect.
Clonidine Transdermal System Side Effect Report#9417429
Application Site Rash
This report suggests a potential Clonidine Transdermal System Usp Application Site Rash side effect(s) that can have serious consequences. A male patient (weight: NA) from US was diagnosed with the following symptoms/conditions: attention deficit/hyperactivity disorder,off label use and used Clonidine Transdermal System Usp (dosage: Q Week) starting NS. After starting Clonidine Transdermal System Usp the patient began experiencing various side effects, including: Application Site RashAdditional drugs used concurrently: NA. Although Clonidine Transdermal System Usp demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Rash, may still occur.
Clonidine Transdermal System Side Effect Report#9417428
Blood Pressure Increased
This Blood Pressure Increased problem was reported by a consumer or non-health professional from US. A 64-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: blood pressure increased. On 2013 this consumer started treatment with Clonidine Transdermal System Usp (dosage: Qw). The following drugs were being taken at the same time:
  • Accupril
  • Amlodipine
When using Clonidine Transdermal System Usp, the patient experienced the following unwanted symptoms/side effects: Blood Pressure IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Pressure Increased, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9417426
Blood Pressure Increased
This Blood Pressure Increased side effect was reported by a pharmacist from US. A 83-year-old female patient (weight:NA) experienced the following symptoms/conditions: blood pressure.The patient was prescribed Clonidine Transdermal System Usp (drug dosage: Qw), which was initiated on
Apr 04, 2013. Concurrently used drugs:
  • Norvasc
  • Spironolactone
.After starting to take Clonidine Transdermal System Usp the consumer reported adverse symptoms, such as: Blood Pressure IncreasedThese side effects may potentially be related to Clonidine Transdermal System Usp.
Clonidine Transdermal System Side Effect Report#9417423
Pain In Extremity
This is a report of a 56-year-old male patient (weight: NA) from US, suffering from the following health symptoms/conditions: pain in extremity,off label use,complex regional pain syndrome, who was treated with Clonidine Transdermal System Usp (dosage: One Patch To Each Food Every 4 Days, start time:
Apr 09, 2013), combined with: NA. and developed a serious reaction and side effect(s): Pain In Extremity after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System Usp treatment in male patients, resulting in Pain In Extremity side effect.
Clonidine Transdermal System Side Effect Report#9255196
Application Site Erythema, Application Site Pruritus
This report suggests a potential Clonidine Transdermal System Usp Application Site Erythema side effect(s) that can have serious consequences. A 58-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: hypertension and used Clonidine Transdermal System Usp (dosage: Changed Qw) starting 201212. After starting Clonidine Transdermal System Usp the patient began experiencing various side effects, including: Application Site Erythema, Application Site PruritusAdditional drugs used concurrently: NA. Although Clonidine Transdermal System Usp demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Erythema, may still occur.
Clonidine Transdermal System Side Effect Report#9255194
Application Site Rash
This Application Site Rash problem was reported by a consumer or non-health professional from US. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: blood pressure increased. On 201202 this consumer started treatment with Clonidine Transdermal System Usp (dosage: Changes Q.w.). The following drugs were being taken at the same time: NA. When using Clonidine Transdermal System Usp, the patient experienced the following unwanted symptoms/side effects: Application Site RashAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Application Site Rash, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9255187
Headache, Asthenia, Pain
This Headache side effect was reported by a physician from US. A 83-year-old female patient (weight:NA) experienced the following symptoms/conditions: blood pressure increased.The patient was prescribed Clonidine Transdermal System Usp (drug dosage: Change Weekly), which was initiated on
Jan 02, 2013. Concurrently used drugs:
  • Diovan
  • Indapamide
.After starting to take Clonidine Transdermal System Usp the consumer reported adverse symptoms, such as: Headache, Asthenia, PainThese side effects may potentially be related to Clonidine Transdermal System Usp.
Clonidine Transdermal System Side Effect Report#9255185
Dysgeusia, Dizziness, Nausea
This is a report of a 68-year-old male patient (weight: NA) from US, suffering from the following health symptoms/conditions: blood pressure increased, who was treated with Clonidine Transdermal System Usp (dosage: Qw, start time:
Dec 31, 2012), combined with:
  • Metoprolol
  • Enalapril
  • Hctz
and developed a serious reaction and side effect(s): Dysgeusia, Dizziness, Nausea after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System Usp treatment in male patients, resulting in Dysgeusia side effect.
Clonidine Transdermal System Side Effect Report#9255184
Blood Pressure Increased
This report suggests a potential Clonidine Transdermal System Usp Blood Pressure Increased side effect(s) that can have serious consequences. A 54-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: blood pressure increased and used Clonidine Transdermal System Usp (dosage: Changed Qw) starting 201205. After starting Clonidine Transdermal System Usp the patient began experiencing various side effects, including: Blood Pressure IncreasedAdditional drugs used concurrently:
  • Diovan
  • Diuretic
Although Clonidine Transdermal System Usp demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Increased, may still occur.
Clonidine Transdermal System Side Effect Report#9064156
Application Site Pruritus, Rash Macular, Application Site Reaction
This Application Site Pruritus problem was reported by a consumer or non-health professional from US. A 77-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: blood pressure increased. On 201106 this consumer started treatment with Clonidine Transdermal System (dosage: Changes Q 5 Days). The following drugs were being taken at the same time: NA. When using Clonidine Transdermal System, the patient experienced the following unwanted symptoms/side effects: Application Site Pruritus, Rash Macular, Application Site ReactionAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Application Site Pruritus, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9064155
Anxiety
This Anxiety side effect was reported by a consumer or non-health professional from US. A 70-year-old male patient (weight:NA) experienced the following symptoms/conditions: blood pressure increased.The patient was prescribed Clonidine Transdermal System (drug dosage: Changes Q.w.), which was initiated on 201211. Concurrently used drugs: NA..After starting to take Clonidine Transdermal System the consumer reported adverse symptoms, such as: AnxietyThese side effects may potentially be related to Clonidine Transdermal System.
Clonidine Transdermal System Side Effect Report#9064153
Hypertension
This is a report of a 68-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: hypertension, who was treated with Clonidine Transdermal System (dosage: Q Week, start time: 201206), combined with:
  • Labetalol
  • Lisinopril
and developed a serious reaction and side effect(s): Hypertension after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System treatment in female patients, resulting in Hypertension side effect.
Clonidine Transdermal System Side Effect Report#9064151
Tachycardia, Dyspnoea, Chills, Hyperhidrosis
This report suggests a potential Clonidine Transdermal System Tachycardia side effect(s) that can have serious consequences. A 24-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: tachycardia and used Clonidine Transdermal System (dosage: Qweek) starting 201209. After starting Clonidine Transdermal System the patient began experiencing various side effects, including: Tachycardia, Dyspnoea, Chills, HyperhidrosisAdditional drugs used concurrently: NA. Although Clonidine Transdermal System demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Tachycardia, may still occur.
Clonidine Transdermal System Side Effect Report#9064147
Application Site Erythema, Application Site Pruritus
This Application Site Erythema problem was reported by a consumer or non-health professional from US. A 66-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On 201206 this consumer started treatment with Clonidine Transdermal System (dosage: Changed Qw). The following drugs were being taken at the same time: NA. When using Clonidine Transdermal System, the patient experienced the following unwanted symptoms/side effects: Application Site Erythema, Application Site PruritusAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Application Site Erythema, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9064145
Application Site Erythema, Application Site Pruritus
This Application Site Erythema side effect was reported by a consumer or non-health professional from US. A 85-year-old female patient (weight:NA) experienced the following symptoms/conditions: blood pressure increased,adhesion.The patient was prescribed Clonidine Transdermal System (drug dosage: Change Weekly), which was initiated on 201207. Concurrently used drugs: NA..After starting to take Clonidine Transdermal System the consumer reported adverse symptoms, such as: Application Site Erythema, Application Site PruritusThese side effects may potentially be related to Clonidine Transdermal System.
Clonidine Transdermal System Side Effect Report#9064142
Application Site Erythema
This is a report of a 14-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: pain,off label use,gastroenteritis, who was treated with Clonidine Transdermal System (dosage: Changed Qw, start time: 201205), combined with: NA. and developed a serious reaction and side effect(s): Application Site Erythema after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System treatment in female patients, resulting in Application Site Erythema side effect.
Clonidine Transdermal System Side Effect Report#9064140
Blood Pressure Increased
This report suggests a potential Clonidine Transdermal System Blood Pressure Increased side effect(s) that can have serious consequences. A 68-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: blood pressure increased and used Clonidine Transdermal System (dosage: Changed Qw) starting
Oct 15, 2012. After starting Clonidine Transdermal System the patient began experiencing various side effects, including: Blood Pressure IncreasedAdditional drugs used concurrently: NA. Although Clonidine Transdermal System demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Increased, may still occur.
Clonidine Transdermal System Side Effect Report#9064138
Blood Pressure Increased
This Blood Pressure Increased problem was reported by a consumer or non-health professional from US. A 74-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: blood pressure increased. On
Sep 25, 2012 this consumer started treatment with Clonidine Transdermal System (dosage: Change Weekly). The following drugs were being taken at the same time:
  • Ntg
  • Toprol (Xl)
When using Clonidine Transdermal System, the patient experienced the following unwanted symptoms/side effects: Blood Pressure IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Pressure Increased, may become evident only after a product is in use by the general population.
Clonidine Transdermal System Side Effect Report#9064135
Application Site Rash
This Application Site Rash side effect was reported by a physician from US. A 55-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension,diabetes mellitus.The patient was prescribed Clonidine Transdermal System (drug dosage: Q Week), which was initiated on 201207. Concurrently used drugs:
  • Oral Antidiabetics
.After starting to take Clonidine Transdermal System the consumer reported adverse symptoms, such as: Application Site RashThese side effects may potentially be related to Clonidine Transdermal System.
Clonidine Transdermal System Side Effect Report#8871337
Blood Pressure Increased
This is a report of a 70-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: hypertension, who was treated with Clonidine Transdermal System (dosage: Changes Every Week, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Blood Pressure Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Clonidine Transdermal System treatment in female patients, resulting in Blood Pressure Increased side effect.


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The appearance of Clonidine Transdermal System on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Clonidine Transdermal System reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Clonidine Transdermal System Safety Alerts, Active Ingredients, Usage Information

    NDC0591-3508
    TypeHUMAN PRESCRIPTION DRUG
    Proprietary NameClonidine transdermal system
    NameClonidine
    Dosage FormPATCH
    RouteTRANSDERMAL
    On market since20140506
    LabelerActavis Pharma, Inc.
    Active Ingredient(s)CLONIDINE
    Strength(s)0.1
    Unit(s)mg/d
    Pharma ClassAdrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

    More About Clonidine transdermal system

    Side Effects reported to FDA: 30

    Clonidine Transdermal System safety alerts: No

    Reported hospitalizations: 1

    Latest Clonidine Transdermal System clinical trials