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Permethrin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 11. View All

Permethrin FDA safety alerts: No

Reported hospitalizations: 4

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Often additional risks of using a medication, such as Permethrin, 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 Permethrin users, Learn more about unwanted side effects & find ways to reduce them. Browse Permethrin Adverse Reports reported to FDA and participate in Permethrin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Permethrin. 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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Permethrin Adverse Effect Reports (FDA)

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6943121-1 | Anaphylactic Reaction
on Aug 25, 2010 Female patient from UNITED STATES , 60 years of age, weighting 238.1 lb, was diagnosed with acarodermatitis and was treated with Permethrin (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction. Permethrin dosage: .

6924350-X | Rash Pruritic
Patient was taking Permethrin (View Usage). Patient had the following side effects: rash pruritic on Aug 11, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 154.0 lb, was diagnosed with acarodermatitis and. Permethrin dosage: Topically.

6906213-9 | Guillain-barre Syndrome, Muscular Weakness, Paraesthesia
Adverse event was reported on Jul 30, 2010 by a Female patient taking Permethrin (View Usage) (Dosage: 1 Application, Single) was diagnosed with acarodermatitis, bronchitis (What is bronchitis?) and. Location: UNITED STATES , 70 years of age, weighting 155.0 lb, After Permethrin was administered, patient had the following side effects: guillain-barre syndrome (What is guillain-barre syndrome?), muscular weakness, paraesthesia. During the same period patient was treated with PREDNISONE (Unk, Daily) (View Prednisone Review and Prednisone Label ), ANTIBIOTICS (Unk, Daily) (View Antibiotics Review and Antibiotics Label ). Patient was hospitalized.

6441682-2 | Eye Swelling, Swelling Face, Urticaria
on Nov 13, 2009 Male patient from UNITED STATES , weighting 29.98 lb, was diagnosed with acarodermatitis and was treated with Permethrin (View Usage). Patient experienced the following unwanted or unexpected effects: eye swelling, swelling face, urticaria. Permethrin dosage: Applied From Neck To Toes Once Topical.


6414676-0 | Arthralgia, Dermatitis, Hypersensitivity, Impaired Healing, Inflammation, Leukocytoclastic Vasculitis, Oedema Peripheral, Tendon Rupture
on Oct 14, 2009 Male patient from UNITED STATES , 49 years of age, weighting 198.0 lb, was diagnosed with pruritus, rash (What is rash?) and was treated with Permethrin (View Usage). Patient had the following side effects: arthralgia, dermatitis, hypersensitivity, impaired healing, inflammation, leukocytoclastic vasculitis, oedema peripheral, tendon rupture. Permethrin dosage: 1 Application, Twice In 3 Days, Topical. During the same period patient was treated with ANALGESICS (View Analgesics Review and Analgesics Label ). Patient was hospitalized.

6260987-1 | Alcoholism, Anxiety
Patient was taking Permethrin (View Usage). After Permethrin was administered, patient had the following side effects: alcoholism (What is alcoholism?), anxiety (What is anxiety?) on Jun 29, 2009 from UNITED STATES Additional patient health information: Female patient , 68 years of age, weighting 136.9 lb, was diagnosed with acarodermatitis and. Permethrin dosage: One Application, Once, Topical. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6030528-2 | Hypoaesthesia, Paraesthesia, Skin Burning Sensation
Adverse event was reported on Jan 05, 2009 by a Female patient taking Permethrin (View Usage) (Dosage: 60g 5 Times Top) was diagnosed with acarodermatitis and. Location: UNITED STATES , 48 years of age, weighting 128.0 lb, Patient experienced the following unwanted or unexpected effects: hypoaesthesia, paraesthesia, skin burning sensation.

5888774-4 | Burning Sensation, Diarrhoea, Eye Pain, Hypoaesthesia Oral, Lip Swelling, Nausea, Paraesthesia, Pyrexia, Somnolence
on Sep 17, 2008 Female patient from UNITED STATES , 52 years of age, weighting 170.0 lb, was diagnosed with acarodermatitis and was treated with Permethrin (View Usage). Patient had the following side effects: burning sensation, diarrhoea, eye pain, hypoaesthesia oral, lip swelling, nausea (What is nausea?), paraesthesia, pyrexia, somnolence. Permethrin dosage: Layer Of Cream Once Or Twice On Body.

5602018-X | Incorrect Dose Administered, Initial Insomnia, Sensory Disturbance
on Jan 22, 2008 Male patient from CANADA , 33 years of age, weighting 210.0 lb, was treated with Permethrin (View Usage). After Permethrin was administered, patient had the following side effects: incorrect dose administered, initial insomnia, sensory disturbance. Permethrin dosage: . During the same period patient was treated with . (View . Review and . Label ).

5136045-6 | Application Site Irritation, Balance Disorder, Burning Sensation, Dizziness, Dysarthria, Dyspnoea, Headache, Miosis, Muscle Twitching
Patient was taking Permethrin (View Usage). Patient experienced the following unwanted or unexpected effects: application site irritation, balance disorder, burning sensation, dizziness (What is dizziness?), dysarthria, dyspnoea, headache (What is headache?), miosis, muscle twitching on Oct 11, 2006 from UNITED STATES Additional patient health information: Male patient , 47 years of age, weighting 150.0 lb, was diagnosed with acarodermatitis and. Permethrin dosage: Qd; Top. During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ), RID MOUSSE (View Rid Mousse Review and Rid Mousse Label ).

5096951-8 | Abasia, Chest Discomfort, Dizziness, Headache, Lumbar Puncture Abnormal, Nonspecific Reaction
Adverse event was reported on Aug 23, 2006 by a Female patient taking Permethrin (View Usage) (Dosage: X1; Top) was diagnosed with acarodermatitis and. Location: UNITED STATES , 54 years of age, Patient had the following side effects: abasia, chest discomfort, dizziness (What is dizziness?), headache (What is headache?), lumbar puncture abnormal, nonspecific reaction. During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.


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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 Permethrin 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 Permethrin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Permethrin 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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Post Permethrin Side Effect Reporting Your Permethrin side effect will help others recognize and deal with Permethrin side effects. Recent Reports View Permethrin ...

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Permethrin Reactions
Abasia
AlcoholismWhat is Alcoholism?
Anaphylactic Reaction
AnxietyWhat is Anxiety?
Application Site Irritation
Arthralgia
Balance Disorder
Burning Sensation
Chest Discomfort
Dermatitis
Diarrhoea
DizzinessWhat is Dizziness?
Dysarthria
Dyspnoea
Eye Pain
Eye Swelling
Guillain-barre SyndromeWhat is Guillain-barre syndrome?
HeadacheWhat is Headache?
Hypersensitivity
Hypoaesthesia
Hypoaesthesia Oral
Impaired Healing
Incorrect Dose Administered
Inflammation
Initial Insomnia
Leukocytoclastic Vasculitis
Lip Swelling
Lumbar Puncture Abnormal
Miosis
Paraesthesia
Permethrin 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 Permethrin 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!