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Imiquimod adverse events reported to FDA.

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Summary

FDA Adverse Reports: 12. View All

Imiquimod FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 4

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Often additional risks of using a medication, such as Imiquimod, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Imiquimod users, Learn more about unwanted side effects & find ways to reduce them. Browse Imiquimod Adverse Reports reported to FDA and participate in Imiquimod discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Imiquimod. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Imiquimod Adverse Effect Reports (FDA)

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6957430-3 | Application Site Erythema, Application Site Rash, Application Site Reaction, Arthralgia, Autoimmune Disorder, Cutaneous Lupus Erythematosus, Exfoliative Rash, Herpes Zoster
on Aug 02, 2010 Female patient from UNITED STATES , 56 years of age, was diagnosed with lichenoid keratosis and was treated with Imiquimod (View Usage). Patient experienced the following unwanted or unexpected effects: application site erythema, application site rash, application site reaction, arthralgia, autoimmune disorder, cutaneous lupus erythematosus, exfoliative rash, herpes zoster. Imiquimod dosage: 5 Pct;qd;top.

6731423-3 | Headache, Nausea, Pyrexia
Patient was taking Imiquimod (View Usage). Patient had the following side effects: headache (What is headache?), nausea (What is nausea?), pyrexia on May 18, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 57.00 lb, was diagnosed with skin papilloma and. Imiquimod dosage: Apply To Wart Sparingly W/cover Daily Top.

6527913-9 | Pain, Penile Swelling, Pruritus, Rash, Scrotal Swelling, Secretion Discharge, Skin Irritation, Urticaria
Adverse event was reported on Jan 05, 2010 by a Male patient taking Imiquimod (View Usage) (Dosage: ) was diagnosed with anogenital warts and. Location: UNITED STATES , 60 years of age, After Imiquimod was administered, patient had the following side effects: pain (What is pain?), penile swelling, pruritus, rash (What is rash?), scrotal swelling, secretion discharge, skin irritation, urticaria.

6242012-1 | Atrial Fibrillation, Chest Pain, Dizziness, Fall, Feeling Hot
on Jun 10, 2009 Male patient from UNITED STATES , weighting 217.0 lb, was diagnosed with actinic keratosis and was treated with Imiquimod (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (What is atrial fibrillation?), chest pain (What is chest pain?), dizziness (What is dizziness?), fall (What is fall?), feeling hot. Imiquimod dosage: 1 Appl Twice A Week, 060. During the same period patient was treated with ALDARA (1 Appl Twice A Week, 060) (View Aldara Review and Aldara Label ), NORVASC (View Norvasc Review and Norvasc Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), PLAVIX (View Plavix Review and Plavix Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), BRIMONIDINE DROPS (View Brimonidine Drops Review and Brimonidine Drops Label ). Patient was hospitalized.


6028835-2 | Rash
on Jan 05, 2009 Male patient from UNITED STATES , 52 years of age, weighting 219.0 lb, was diagnosed with anogenital warts and was treated with Imiquimod (View Usage). Patient had the following side effects: rash (What is rash?). Imiquimod dosage: Apply At Bedtime Top.

5871871-7 | Acne, Fatigue, Myalgia, Neuropathy Peripheral, Rash Erythematous, Sinusitis, Swelling Face
Patient was taking Imiquimod (View Usage). After Imiquimod was administered, patient had the following side effects: acne (What is acne?), fatigue, myalgia, neuropathy peripheral, rash erythematous, sinusitis (What is sinusitis?), swelling face on Sep 04, 2008 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 180.0 lb, was diagnosed with hyperkeratosis, precancerous skin lesion and. Imiquimod dosage: Tiny Dab Every Second Day Cutaneous.

5738406-0 | Angioedema, Dehydration, Diarrhoea, Hypersensitivity, Hypotension, Hypoxia, Nausea, Renal Failure
Adverse event was reported on May 01, 2008 by a Male patient taking Imiquimod (View Usage) (Dosage: 250 Mg; Biw; Top) was diagnosed with hypertension and. Location: UNITED STATES , 57 years of age, weighting 189.0 lb, Patient experienced the following unwanted or unexpected effects: angioedema, dehydration, diarrhoea, hypersensitivity, hypotension, hypoxia, nausea (What is nausea?), renal failure. During the same period patient was treated with LISINOPRIL (10 Mg; Qd; Po) (View Lisinopril Review and Lisinopril Label ), VITAMIN CAP (View Vitamin Cap Review and Vitamin Cap Label ), MAGNESIUM (View Magnesium Review and Magnesium Label ). Patient was hospitalized.

5725847-0 | Dehydration, Hypersensitivity, Hypotension
on Apr 18, 2008 Male patient from UNITED STATES , 57 years of age, weighting 189.0 lb, was diagnosed with hypertension and was treated with Imiquimod (View Usage). Patient had the following side effects: dehydration, hypersensitivity, hypotension. Imiquimod dosage: 250 Mg;biw;top. During the same period patient was treated with LISINOPRIL (10 Mg) (View Lisinopril Review and Lisinopril Label ), VITAMIN CAP (View Vitamin Cap Review and Vitamin Cap Label ), MAGNESIUM (View Magnesium Review and Magnesium Label ). Patient was hospitalized.

5165516-1 | Application Site Bleeding, Blood Immunoglobulin G Increased, Erythema, Herpes Simplex, Pain, Rash Papular
on Nov 24, 2006 Female patient from NETHERLANDS , 59 years of age, was diagnosed with basal cell carcinoma and was treated with Imiquimod (View Usage). After Imiquimod was administered, patient had the following side effects: application site bleeding, blood immunoglobulin g increased, erythema, herpes simplex (What is herpes simplex?), pain (What is pain?), rash papular. Imiquimod dosage: Topical.

5153414-9 | Accidental Overdose, Application Site Erosion, Bacterial Infection, Ectropion, Keratitis
Patient was taking Imiquimod (View Usage). Patient experienced the following unwanted or unexpected effects: accidental overdose, application site erosion, bacterial infection (What is bacterial infection?), ectropion, keratitis on Oct 26, 2006 from PORTUGAL Additional patient health information: Male patient , 70 years of age, was diagnosed with actinic keratosis and. Imiquimod dosage: 3 Unpsec., 3 In 1 Week(s). Patient was hospitalized.

4918507-7 | Rash
Adverse event was reported on Feb 21, 2006 by a Male patient taking Imiquimod (View Usage) (Dosage: ) . Location: UNITED STATES , 28 years of age, weighting 199.1 lb, Patient had the following side effects: rash (What is rash?).

4893359-2 | Rash
on Jan 25, 2006 Male patient from UNITED STATES , 28 years of age, weighting 199.1 lb, was treated with Imiquimod (View Usage). After Imiquimod was administered, patient had the following side effects: rash (What is rash?). Imiquimod dosage: .


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Imiquimod risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Imiquimod quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Imiquimod use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Imiquimod Reactions
Accidental Overdose
AcneWhat is Acne?
Angioedema
Application Site Bleeding
Application Site Erosion
Application Site Erythema
Application Site Rash
Application Site Reaction
Arthralgia
Atrial FibrillationWhat is Atrial fibrillation?
Autoimmune Disorder
Bacterial InfectionWhat is Bacterial infection?
Blood Immunoglobulin G Increased
Chest PainWhat is Chest pain?
Cutaneous Lupus Erythematosus
Dehydration
Diarrhoea
DizzinessWhat is Dizziness?
Ectropion
Erythema
Exfoliative Rash
FallWhat is Fall?
Fatigue
Feeling Hot
Hypersensitivity
Hypotension
NauseaWhat is Nausea?
PainWhat is Pain?
RashWhat is Rash?
Vomiting
Imiquimod Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Imiquimod adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!