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Aldara Application Site Erythema Side Effects

Aldara Application Site Erythema Side Effect Reports


The following Aldara Application Site Erythema side effect reports were submitted by healthcare professionals and consumers.

This information will help you understand how side effects, such as Application Site Erythema, can occur, and what you can do about them.

A side effect could appear soon after you start Aldara or it might take time to develop.



Candidiasis, Dermatitis, Postictal State, Dysuria, Grand Mal Convulsion, White Blood Cell Count Increased, Cellulitis, Application Site Erythema, Vomiting

This Application Site Erythema side effect was reported by a physician from UNITED STATES. A 2-year-old female patient (weight:NA) experienced the following symptoms/conditions: molluscum contagiosum. The patient was prescribed Aldara (dosage: Qd;top), which was started on NS. Concurrently used drugs: NA. When starting to take Aldara the consumer reported the following symptoms:
  • Candidiasis
  • Dermatitis
  • Postictal State
  • Dysuria
  • Grand Mal Convulsion
  • White Blood Cell Count Increased
  • Cellulitis
  • Application Site Erythema
  • Vomiting
The patient was hospitalized. These side effects may potentially be related to Aldara.
Colitis, Coeliac Disease, Furuncle, Application Site Scab, Gastrointestinal Disorder, Application Site Erythema

This Application Site Erythema Aldara side effect was reported by a physician from UNITED STATES on Feb 28, 2011. A Female , 41 years of age, was diagnosed with and was treated with Aldara. The patient presented the following health conditions:
  • Colitis
  • Coeliac Disease
  • Furuncle
  • Application Site Scab
  • Gastrointestinal Disorder
  • Application Site Erythema
. Aldara dosage: 5 Pct;5xw;top. Additional drugs used at the same time: NA.
Application Site Scab, Application Site Reaction, Coeliac Disease, Colitis, Dyspepsia, Application Site Erythema, Open Wound

This is a Aldara side effect report of a 41-year-old female patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: basal cell carcinoma, who was treated with Aldara (dosage:5 Pct; 5xw; Top, start time: Jan 31, 2009), combined with: NA., and developed a serious reaction and a Application Site Erythema side effect. The patient presented with:
  • Application Site Scab
  • Application Site Reaction
  • Coeliac Disease
  • Colitis
  • Dyspepsia
  • Application Site Erythema
  • Open Wound
which developed after the beginning of treatment. This side effect report can indicate a possible existence of increased vulnerability to Aldara treatment in female patients suffering from basal cell carcinoma, resulting in Application Site Erythema.

Application Site Erythema, Application Site Scab, Application Site Swelling, Lymphadenopathy, Non-small Cell Lung Cancer

A 67-year-old patient (weight: NA) from UNITED STATES with the following symptoms: basal cell carcinoma started Aldara treatment (dosage: 4xw; Top) on NS. Soon after starting Aldara treatment, the consumer experienced several side effects, including:
  • Application Site Erythema
  • Application Site Scab
  • Application Site Swelling
  • Lymphadenopathy
  • Non-small Cell Lung Cancer
. Concurrently used drugs: NA. This finding indicates that some patients can be more vulnerable to developing Aldara side effects, such as Application Site Erythema.
Application Site Abscess, Application Site Cellulitis, Application Site Discharge, Application Site Discolouration, Application Site Erythema, Application Site Infection, Application Site Inflammation, Application Site Pain, Application Site Scab

A female patient from UNITED STATES was prescribed and started Aldara on Jan 12, 2010. Patient felt the following Aldara side effects: application site abscess, application site cellulitis, application site discharge, application site discolouration, application site erythema, application site infection, application site inflammation, application site pain, application site scab Additional patient health information: Female , 57 years of age, weighting 169.0 lb, The consumer reported the following symptoms: was diagnosed with and. Aldara dosage: Q3w; Top. Concurrently used drugs:
  • Bactrim Ds (1 Df; Bid; Po)
  • Prempro
  • Vitamins
The patient was hospitalized.
Application Site Erythema

This report suggests a potential Aldara Application Site Erythema side effect(s) that can have serious consequences. A 47-year-old female patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): squamous cell carcinoma and used Aldara (dosage: Small Drop Apply To Lesion At Bedtime And Surrounding Skin X 3 Weeks) starting Oct 07, 2009. Soon after starting Aldara the patient began experiencing various side effects, including:
  • Application Site Erythema
Drugs used concurrently:NA. Although Aldara demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Erythema, may still occur.
Application Site Erythema, Application Site Irritation, Application Site Pain, Application Site Scab, Application Site Swelling, Application Site Vesicles, Supraventricular Tachycardia

An adverse event was reported by a consumer or non-health professional on Aug 27, 2009 by a Female taking Aldara (dosage: Application - Qd - Topical) was diagnosed with and. Location: CANADA , 51 years of age, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Aldara side effects: application site erythema, application site irritation, application site pain, application site scab, application site swelling, application site vesicles, supraventricular tachycardia. Additional medications/treatments: The patient was hospitalized.
Application Site Discolouration, Application Site Erythema, Application Site Exfoliation, Application Site Reaction, Arthritis, Cough, Dry Skin, Faeces Discoloured

This Application Site Erythema problem was reported by a consumer or non-health professional from UNITED STATES. A 70-year-old patient (weight: NA) was diagnosed with the following medical condition(s): skin cancer.On Jun 17, 2009 a consumer started treatment with Aldara (dosage: 3xw - Topical). The following drugs/medications were being taken at the same time:
  • Hyrochorithiazide/triamterene (dyazide)
  • Prazsoin Hcl
When commencing Aldara, the patient experienced the following unwanted symptoms /side effects:
  • Application Site Discolouration
  • Application Site Erythema
  • Application Site Exfoliation
  • Application Site Reaction
  • Arthritis
  • Cough
  • Dry Skin
  • Faeces Discoloured
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential 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.
Application Site Discharge, Application Site Discolouration, Application Site Erythema, Application Site Infection, Application Site Scab, Breast Infection, Condition Aggravated, Pruritus

This is a Aldara side effect report of a 57-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: precancerous cells present,infection and was treated with Aldara (dosage: Application - 3xw - Topical) starting Jan 12, 2009. Concurrently used drugs:
  • Bactrim (Unk - Unk - Oral)
  • Prempro
Soon after that, the consumer experienced the following of symptoms:
  • Application Site Discharge
  • Application Site Discolouration
  • Application Site Erythema
  • Application Site Infection
  • Application Site Scab
  • Breast Infection
  • Condition Aggravated
  • Pruritus
The patient was hospitalized. This opens a possibility that Aldara could cause Application Site Erythema and that some female patients may be more susceptible.
Application Site Discharge, Application Site Discolouration, Application Site Erythema, Application Site Infection, Application Site Scab, Breast Infection, Condition Aggravated, Precancerous Cells Present, Pruritus

This Application Site Erythema side effect was reported by a consumer or non-health professional from UNITED STATES on May 06, 2009. A female patient from UNITED STATES , 57 years of age, was diagnosed with and was treated with Aldara. Directly after treatment started, patient experienced the unwanted or unexpected Aldara side effects: application site discharge, application site discolouration, application site erythema, application site infection, application site scab, breast infection, condition aggravated, precancerous cells present, pruritus. Aldara dosage: 3xw- Topical.
Associated medications used:
  • Sulfamethoxazole And Trimethoprim (Oral)
  • Conjugated Estrogens/medroxyprogesterone Acetate(prempro)
The patient was hospitalized. These side effects may potentially be related to Aldara.
Application Site Erosion, Application Site Erythema, Application Site Oedema, Cardiac Failure, Keratoacanthoma

This Application Site Erythema side effect was reported by a physician from SWITZERLAND. A 80-year-old female patient (weight:NA) experienced the following symptoms/conditions: actinic keratosis,bowen's disease. The patient was prescribed Aldara (dosage: Application - 2xw - Topical), which was started on NS. Concurrently used drugs: NA. When starting to take Aldara the consumer reported the following symptoms:
  • Application Site Erosion
  • Application Site Erythema
  • Application Site Oedema
  • Cardiac Failure
  • Keratoacanthoma
The patient was hospitalized. These side effects may potentially be related to Aldara.
Application Site Erythema, Application Site Swelling, Arthralgia, Back Pain, Central Nervous System Lesion, Headache, Hypertension, Lymphadenopathy

This Application Site Erythema Aldara side effect was reported by a consumer or non-health professional from UNITED STATES on Feb 29, 2008. A male , 47 years of age, was diagnosed with and was treated with Aldara. The patient presented the following health conditions:
  • Application Site Erythema
  • Application Site Swelling
  • Arthralgia
  • Back Pain
  • Central Nervous System Lesion
  • Headache
  • Hypertension
  • Lymphadenopathy
. Aldara dosage: Application - 4 Times Weekly - Topical. Additional drugs used at the same time: NA. The patient was hospitalized.
Application Site Discharge, Application Site Erythema, Application Site Irritation, Application Site Reaction, Application Site Scab, Coagulopathy, Skin Discolouration, Skin Necrosis, Thrombocytopenia

This is a Aldara side effect report of a 77-year-old patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: actinic keratosis,basal cell carcinoma, who was treated with Aldara (dosage:5xw; Topical, start time: Jul 01, 2007), combined with: NA., and developed a serious reaction and a Application Site Erythema side effect. The patient presented with:
  • Application Site Discharge
  • Application Site Erythema
  • Application Site Irritation
  • Application Site Reaction
  • Application Site Scab
  • Coagulopathy
  • Skin Discolouration
  • Skin Necrosis
  • Thrombocytopenia
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Aldara treatment in patients suffering from actinic keratosis,basal cell carcinoma, resulting in Application Site Erythema.
Application Site Discharge, Application Site Erythema, Application Site Scab, Coagulopathy, Incorrect Dose Administered

A 77-year-old patient (weight: NA) from UNITED STATES with the following symptoms: actinic keratosis started Aldara treatment (dosage: Application - 5xw - Topical) on Aug 06, 2007. Soon after starting Aldara treatment, the consumer experienced several side effects, including:
  • Application Site Discharge
  • Application Site Erythema
  • Application Site Scab
  • Coagulopathy
  • Incorrect Dose Administered
. Concurrently used drugs: NA. This finding indicates that some patients can be more vulnerable to developing Aldara side effects, such as Application Site Erythema.
Application Site Discolouration, Application Site Erythema, Application Site Irritation, Application Site Scab, Hypercoagulation, Overdose, Skin Discolouration

A patient from UNITED STATES was prescribed and started Aldara on Oct 22, 2007. After Aldara was administered, patient encountered several Aldara side effects: application site discolouration, application site erythema, application site irritation, application site scab, hypercoagulation, overdose, skin discolouration Additional patient health information: male , 70 years of age, The consumer reported the following symptoms: . Aldara dosage: Topical. Concurrently used drugs: NA. The patient was hospitalized.
Application Site Erythema, Application Site Irritation, Application Site Scab, Blood Pressure Increased, Bronchitis, Haematochezia, Oral Herpes, Urinary Tract Infection

This report suggests a potential Aldara Application Site Erythema side effect(s) that can have serious consequences. A 68-year-old female patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): basal cell carcinoma,biopsy and used Aldara (dosage: Application - 7xw- Topical) starting Jun 02, 2007. Soon after starting Aldara the patient began experiencing various side effects, including:
  • Application Site Erythema
  • Application Site Irritation
  • Application Site Scab
  • Blood Pressure Increased
  • Bronchitis
  • Haematochezia
  • Oral Herpes
  • Urinary Tract Infection
Drugs used concurrently:NA. The patient was hospitalized. Although Aldara demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Erythema, may still occur.
Application Site Erythema, Application Site Pruritus, C-reactive Protein Increased, Fatigue, Influenza Like Illness, Myalgia, Red Blood Cell Sedimentation Rate Increased

An adverse event was reported by a consumer or non-health professional on Feb 16, 2007 by a male taking Aldara (dosage: 0.5 Df, 5 Times Weekly (0.5 Dosage Forms, 5 In 1 Week(s))) was diagnosed with and. Location: FRANCE , 75 years of age, patient began experiencing various side effects, including: Patient felt the following Aldara side effects: application site erythema, application site pruritus, c-reactive protein increased, fatigue, influenza like illness, myalgia, red blood cell sedimentation rate increased. Additional medications/treatments:
Multiple prescriptions taken:
  • Xatral Lp (alufuzosin Hydrochloride)
  • Prednisone
  • Methotrexate
Application Site Discharge, Application Site Erythema, Application Site Pain, Application Site Swelling, Cellulitis, Pyrexia

This Application Site Erythema problem was reported by a physician from UNITED STATES. A 26-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): anogenital warts.On Jan 21, 2007 a consumer started treatment with Aldara (dosage: (unk 2 Total), Topical). The following drugs/medications were being taken at the same time: NA. When commencing Aldara, the patient experienced the following unwanted symptoms /side effects:
  • Application Site Discharge
  • Application Site Erythema
  • Application Site Pain
  • Application Site Swelling
  • Cellulitis
  • Pyrexia
Although all drugs are carefully tested before they are licensed for use, they carry potential 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.
Application Site Erythema, Application Site Inflammation, Application Site Reaction, Asthenia, Dizziness, Fatigue, Hypotension, Platelet Count Decreased, Scar

This is a Aldara side effect report of a 65-year-old patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: basal cell carcinoma and was treated with Aldara (dosage: 1 Sachet, 5 In Week(s), Topical) starting Jan 01, 2006. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
  • Application Site Erythema
  • Application Site Inflammation
  • Application Site Reaction
  • Asthenia
  • Dizziness
  • Fatigue
  • Hypotension
  • Platelet Count Decreased
  • Scar
The patient was hospitalized. This opens a possibility that Aldara could cause Application Site Erythema and that some patients may be more susceptible.
Application Site Erythema, Application Site Irritation, Application Site Pain, Application Site Pruritus, Application Site Reaction, Dizziness, Hypotension, Influenza Like Illness, Insomnia

This Application Site Erythema side effect was reported by a consumer or non-health professional from UNITED STATES on Aug 03, 2006. A female patient from UNITED STATES , 62 years of age, was diagnosed with and was treated with Aldara. Patient felt the following Aldara side effects: application site erythema, application site irritation, application site pain, application site pruritus, application site reaction, dizziness, hypotension, influenza like illness, insomnia. Aldara dosage: 1 Sachet, 3 In 1 Week(s)), Topical. These side effects may potentially be related to Aldara.
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DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Aldara Application Site Erythema Causes and Reviews


We are sorry, but no medical information on this topic currently exists in our database. Our articles are updated often, please revisit soon.


Aldara Application Site Erythema Reviews

Sat, 21 Jan 2012

Symptoms of an overdose, flu, headache, chest pain, back pain, mental distress and anxiety.  Long term effects still occurring with respiratory distress (used it on my chest).  I feel my airways have been damaged.  

Sat, 18 Feb 2012

Got a huge painful mouth ulcer, cough and upper lip inflamation. I told the doctor who prescribed them that I was being investigated for an automune disorder but noone seemed worried!!! So irresponsible its unreal. I mean who the hell does this? Doctors dont have a bloody clue.... just cos they've got the title they think theyre kings of the world.... and you dont need to be a rocket scientist to figure out what i did!!!!

Fri, 09 Dec 2011

Told by dermatologist to apply Aldara to chest area three times per week to eliminate precancer third week started getting red sores on chest so i called the Quack and was told this was normal and continue applying. By the forth week i was getting very tired and my whole body hurt like i had the flu so i quit applying Aldara. Flu feeling intensified as well as feeling sick to my stomach and a major headache and my back hurt as well as my Bones and feet. I felt like i had cancer now. Called my dermatologist in mean Quack and told him my symptoms he told me that they were not related to the Aldara and to see my primary care doctor. Primary care doctor told me it was from the Aldara that i should have stopped putting it on when the sores appeared.
He gave me pain meds and told me that it should be out of my system in 2 -3 weeks. fifth week no change second week off work. Sixth week the flu symptoms and and bone pain and back pain disappeared. Sixth week now still tired with major headache and nausea. I'm praying these disappear.

Sat, 09 Jan 2010
I have been using Aldara for the last month and began developing reactions (redface, swelling at sight). Given the reactions I'm experiencing using Aldara, I was wondering if it would be safe to get the seasonal and H1N1 vaccinations while taking Aldara?
Thu, 17 Feb 2011
I have suffered injury from Aldara and want to know if there is anyone else out there that has been injured .
DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

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Top Aldara Side Effects

Application Site Erythema (50)
Fatigue (46)
Influenza Like Illness (41)
Application Site Reaction (37)
Headache (33)
Dizziness (30)
Erythema (24)
Application Site Pain (23)
Application Site Irritation (22)
Application Site Scab (19)
Arthralgia (18)
Back Pain (18)
Pyrexia (18)
Lymphadenopathy (18)
Nausea (17)
Dyspnoea (17)
Diarrhoea (17)
Application Site Inflammation (16)
Pain (16)
Asthenia (16)
Myalgia (15)
Inflammation (12)
Application Site Pruritus (12)
Malaise (12)
Scab (12)
Balance Disorder (11)
Pruritus (10)
Burning Sensation (10)
Condition Aggravated (10)
Application Site Discharge (9)
Application Site Oedema (9)
Vision Blurred (9)
Application Site Ulcer (9)
Eczema (9)
Chills (8)
Blood Pressure Increased (8)
Dysuria (8)
Feeling Abnormal (8)
Skin Discolouration (8)
Application Site Infection (7)
Application Site Discolouration (7)
Anaemia (7)
Alanine Aminotransferase Increased (7)
Application Site Swelling (7)
Blister (7)
Palpitations (7)
Gait Disturbance (7)
Erythema Multiforme (7)
Chest Pain (7)
Aspartate Aminotransferase Increased (7)

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