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Aldara Application Site Reaction Side Effects

Aldara Application Site Reaction Side Effect Reports


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

This information will help you understand how side effects, such as Application Site Reaction, 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.



Asthenia, Decreased Appetite, Weight Decreased, Application Site Reaction

This Application Site Reaction side effect was reported by a consumer or non-health professional from US. A 90-year-old female patient (weight:NA) experienced the following symptoms/conditions: acne. The patient was prescribed Aldara (dosage: NA), which was started on 201205. Concurrently used drugs: NA. When starting to take Aldara the consumer reported the following symptoms:
  • Asthenia
  • Decreased Appetite
  • Weight Decreased
  • Application Site Reaction
The patient was hospitalized. These side effects may potentially be related to Aldara.
Application Site Scab, Application Site Reaction, Coeliac Disease, Colitis, Dyspepsia, Application Site Erythema, Open Wound

This Application Site Reaction Aldara side effect was reported by a physician from UNITED STATES on Feb 24, 2011. A Female , 41 years of age, was diagnosed with and was treated with Aldara. The patient presented the following health conditions:
  • Application Site Scab
  • Application Site Reaction
  • Coeliac Disease
  • Colitis
  • Dyspepsia
  • Application Site Erythema
  • Open Wound
. Aldara dosage: 5 Pct; 5xw; Top. Additional drugs used at the same time: NA.
Application Site Discolouration, Application Site Erythema, Application Site Exfoliation, Application Site Reaction, Arthritis, Cough, Dry Skin, Faeces Discoloured

This is a Aldara side effect report of a 70-year-old patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: skin cancer, who was treated with Aldara (dosage:3xw - Topical, start time: Jun 17, 2009), combined with:
  • Hyrochorithiazide/triamterene (dyazide)
  • Prazsoin Hcl
, and developed a serious reaction and a Application Site Reaction side effect. The patient presented with:
  • Application Site Discolouration
  • Application Site Erythema
  • Application Site Exfoliation
  • Application Site Reaction
  • Arthritis
  • Cough
  • Dry Skin
  • Faeces Discoloured
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 skin cancer, resulting in Application Site Reaction.

Agitation, Application Site Inflammation, Application Site Reaction, Application Site Swelling, Application Site Warmth, Confusional State

A 84-year-old female patient (weight: NA) from UNITED STATES with the following symptoms: skin cancer started Aldara treatment (dosage: Cover Wound Daily 5 Days A Wee Transdermal) on May 15, 2009. Soon after starting Aldara treatment, the consumer experienced several side effects, including:
  • Agitation
  • Application Site Inflammation
  • Application Site Reaction
  • Application Site Swelling
  • Application Site Warmth
  • Confusional State
. Concurrently used drugs: NA. This finding indicates that some patients can be more vulnerable to developing Aldara side effects, such as Application Site Reaction.
Application Site Reaction, Autoimmune Disorder, Chest Discomfort, Deafness, Dry Eye, Dry Mouth, Dyspnoea, Erythema, Gastrointestinal Pain

A female patient from UNITED STATES was prescribed and started Aldara on Nov 05, 2008. Patient felt the following Aldara side effects: application site reaction, autoimmune disorder, chest discomfort, deafness, dry eye, dry mouth, dyspnoea, erythema, gastrointestinal pain Additional patient health information: Female , 52 years of age, weighting 105.0 lb, The consumer reported the following symptoms: was diagnosed with and. Aldara dosage: One Packet 4 Times Week/8 Wk. Concurrently used drugs: NA.
Abdominal Pain Upper, Application Site Reaction, Blister, Chest Pain, Dyspnoea, Influenza Like Illness, Lymphadenopathy

This report suggests a potential Aldara Application Site Reaction side effect(s) that can have serious consequences. A 46-year-old patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): hyperkeratosis and used Aldara (dosage: Spot Treatment 3 Times A Week Top) starting Jun 13, 2008. Soon after starting Aldara the patient began experiencing various side effects, including:
  • Abdominal Pain Upper
  • Application Site Reaction
  • Blister
  • Chest Pain
  • Dyspnoea
  • Influenza Like Illness
  • Lymphadenopathy
Drugs used concurrently:NA. Although Aldara demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Reaction, may still occur.
Activities Of Daily Living Impaired, Application Site Reaction, Arthropathy, Polymyositis, Weight Decreased

An adverse event was reported by a consumer or non-health professional on Apr 16, 2008 by a male taking Aldara (dosage: .22 G 3x/week Top) was diagnosed with and. Location: UNITED STATES , 58 years of age, weighting 178.0 lb, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Aldara side effects: activities of daily living impaired, application site reaction, arthropathy, polymyositis, weight decreased. Additional medications/treatments:
Application Site Discharge, Application Site Erythema, Application Site Irritation, Application Site Reaction, Application Site Scab, Coagulopathy, Skin Discolouration, Skin Necrosis, Thrombocytopenia

This Application Site Reaction problem was reported by a physician from UNITED STATES. A 77-year-old patient (weight: NA) was diagnosed with the following medical condition(s): actinic keratosis,basal cell carcinoma.On Jul 01, 2007 a consumer started treatment with Aldara (dosage: 5xw; 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 Irritation
  • Application Site Reaction
  • Application Site Scab
  • Coagulopathy
  • Skin Discolouration
  • Skin Necrosis
  • Thrombocytopenia
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 Reaction, may become evident only after a product is in use by the general population.
Application Site Reaction, Application Site Scab, Erythema Multiforme, Localised Infection

This is a Aldara side effect report of a 58-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: actinic keratosis,basal cell carcinoma and was treated with Aldara (dosage: (0.5 Sachet, 5 In 1 Week(s), Topical) starting Dec 25, 2006. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
  • Application Site Reaction
  • Application Site Scab
  • Erythema Multiforme
  • Localised Infection
This opens a possibility that Aldara could cause Application Site Reaction and that some female patients may be more susceptible.
Application Site Reaction, Erythema Multiforme, Herpes Zoster, Oral Intake Reduced, Staphylococcal Infection, Toxic Epidermal Necrolysis

This Application Site Reaction side effect was reported by a physician from UNITED STATES on Jan 17, 2007. A female patient from UNITED STATES , 58 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 reaction, erythema multiforme, herpes zoster, oral intake reduced, staphylococcal infection, toxic epidermal necrolysis. Aldara dosage: 0.5 Scahet, 5 In 1 Weeks (s)), Topical. These side effects may potentially be related to Aldara.
Application Site Inflammation, Application Site Reaction, Dysuria, Pain, Urinary Retention, Vaginal Laceration

This Application Site Reaction side effect was reported by a consumer or non-health professional from IRELAND. A 20-year-old female patient (weight:NA) experienced the following symptoms/conditions: anogenital warts. The patient was prescribed Aldara (dosage: NA), which was started on Nov 15, 2006. Concurrently used drugs: NA. When starting to take Aldara the consumer reported the following symptoms:
  • Application Site Inflammation
  • Application Site Reaction
  • Dysuria
  • Pain
  • Urinary Retention
  • Vaginal Laceration
These side effects may potentially be related to Aldara.
Application Site Pain, Application Site Reaction, Application Site Scab, Impaired Healing, Squamous Cell Carcinoma, Ulcer

This Application Site Reaction Aldara side effect was reported by a physician from UNITED STATES on Oct 18, 2006. A Female , 39 years of age, was diagnosed with and was treated with Aldara. The patient presented the following health conditions:
  • Application Site Pain
  • Application Site Reaction
  • Application Site Scab
  • Impaired Healing
  • Squamous Cell Carcinoma
  • Ulcer
. Aldara dosage: (5 In 1 Week(s)), Topical. Additional drugs used at the same time: NA.
Application Site Reaction, Erythema, Eye Irritation, Inflammation, Ocular Hyperaemia, Vision Blurred

This is a Aldara side effect report of a 61-year-old patient (weight:NA) from SPAIN, suffering from the following symptoms/conditions: skin papilloma, who was treated with Aldara (dosage:1 (1, 1 In 1 Day (s)) Topical, start time: Sep 11, 2006), combined with: NA., and developed a serious reaction and a Application Site Reaction side effect. The patient presented with:
  • Application Site Reaction
  • Erythema
  • Eye Irritation
  • Inflammation
  • Ocular Hyperaemia
  • Vision Blurred
which developed after the beginning of treatment. This side effect report can indicate a possible existence of increased vulnerability to Aldara treatment in patients suffering from skin papilloma, resulting in Application Site Reaction.
Application Site Erythema, Application Site Inflammation, Application Site Reaction, Asthenia, Dizziness, Fatigue, Hypotension, Platelet Count Decreased, Scar

A 65-year-old patient (weight: NA) from UNITED STATES with the following symptoms: basal cell carcinoma started Aldara treatment (dosage: 1 Sachet, 5 In Week(s), Topical) on Jan 01, 2006. Soon after starting Aldara treatment, the consumer experienced several side effects, including:
  • Application Site Erythema
  • Application Site Inflammation
  • Application Site Reaction
  • Asthenia
  • Dizziness
  • Fatigue
  • Hypotension
  • Platelet Count Decreased
  • Scar
. Concurrently used drugs: NA.The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Aldara side effects, such as Application Site Reaction.
Application Site Erythema, Application Site Irritation, Application Site Pain, Application Site Pruritus, Application Site Reaction, Dizziness, Hypotension, Influenza Like Illness, Insomnia

A female patient from UNITED STATES was prescribed and started Aldara on Aug 03, 2006. After Aldara was administered, patient encountered several Aldara side effects: application site erythema, application site irritation, application site pain, application site pruritus, application site reaction, dizziness, hypotension, influenza like illness, insomnia Additional patient health information: Female , 62 years of age, The consumer reported the following symptoms: was diagnosed with and. Aldara dosage: 1 Sachet, 3 In 1 Week(s)), Topical. Concurrently used drugs: NA.
Anxiety, Application Site Dryness, Application Site Pain, Application Site Pruritus, Application Site Reaction, Fatigue, Feeling Cold, Mental Disorder, Myalgia

This report suggests a potential Aldara Application Site Reaction side effect(s) that can have serious consequences. A 56-year-old female patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): anogenital warts and used Aldara (dosage: See Image) starting May 31, 2006. Soon after starting Aldara the patient began experiencing various side effects, including:
  • Anxiety
  • Application Site Dryness
  • Application Site Pain
  • Application Site Pruritus
  • Application Site Reaction
  • Fatigue
  • Feeling Cold
  • Mental Disorder
  • Myalgia
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 Reaction, may still occur.
Application Site Erythema, Application Site Reaction, Cutaneous Lupus Erythematosus, Post Procedural Complication, Post Procedural Oedema, Procedural Pain

An adverse event was reported by a health professional on May 18, 2006 by a Female taking Aldara (dosage: (2 In 1 Week (s)), Topical) was diagnosed with and. Location: UNITED STATES , 55 years of age, patient began experiencing various side effects, including: Patient felt the following Aldara side effects: application site erythema, application site reaction, cutaneous lupus erythematosus, post procedural complication, post procedural oedema, procedural pain. Additional medications/treatments:
Alanine Aminotransferase Increased, Application Site Erythema, Application Site Reaction, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Iron Increased, Liver Function Test Abnormal, Scab

This Application Site Reaction problem was reported by a consumer or non-health professional from UNITED STATES. A 82-year-old patient (weight: NA) was diagnosed with the following medical condition(s): basal cell carcinoma.On Jun 08, 2005 a consumer started treatment with Aldara (dosage: See Image). The following drugs/medications were being taken at the same time: NA. When commencing Aldara, the patient experienced the following unwanted symptoms /side effects:
  • Alanine Aminotransferase Increased
  • Application Site Erythema
  • Application Site Reaction
  • Aspartate Aminotransferase Increased
  • Blood Alkaline Phosphatase Increased
  • Blood Iron Increased
  • Liver Function Test Abnormal
  • Scab
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 Reaction, may become evident only after a product is in use by the general population.
Application Site Erythema, Application Site Oedema, Application Site Pain, Application Site Reaction, Dehydration, Dysgeusia, Dyspepsia, Headache

This is a Aldara side effect report of a 52-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: basal cell carcinoma and was treated with Aldara (dosage: See Image) starting Apr 06, 2005. Concurrently used drugs:
  • Multivitamin
Soon after that, the consumer experienced the following of symptoms:
  • Application Site Erythema
  • Application Site Oedema
  • Application Site Pain
  • Application Site Reaction
  • Dehydration
  • Dysgeusia
  • Dyspepsia
  • Headache
This opens a possibility that Aldara could cause Application Site Reaction and that some female patients may be more susceptible.
Accidental Exposure, Application Site Erythema, Application Site Pruritus, Application Site Reaction

This Application Site Reaction side effect was reported by a consumer or non-health professional from UNITED STATES on Mar 25, 2006. A female patient from UNITED STATES , 76 years of age, was diagnosed with and was treated with Aldara. Patient felt the following Aldara side effects: accidental exposure, application site erythema, application site pruritus, application site reaction. Aldara dosage: 1 Sachet, 3 In 1 Week(s), Topical.
Multiple prescriptions taken:
  • Synthroid
  • Aspirin
These side effects may potentially be related to Aldara.

DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Aldara Application Site Reaction Causes and Reviews


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Aldara Application Site Reaction 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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