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Zaditen adverse events reported to FDA.

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Summary

FDA Adverse Reports: 150. View All

Zaditen FDA safety alerts: No

Reported hospitalizations: 45

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2Hormone Disbalance
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Often additional risks of using a medication, such as Zaditen, 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 Zaditen users, Learn more about unwanted side effects & find ways to reduce them. Browse Zaditen Adverse Reports reported to FDA and participate in Zaditen discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Zaditen. 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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Zaditen Adverse Effect Reports (FDA)

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Showing 1-50 of 150  Next Page  >

7007996-2 | Alanine Aminotransferase Increased, Blood Bilirubin Increased, Hepatitis Acute
on Sep 10, 2010 Female patient from ITALY , 48 years of age, was diagnosed with asthma (What is asthma?) and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, blood bilirubin increased, hepatitis acute. Zaditen dosage: Unk. During the same period patient was treated with DIFIX (Unk) (View Difix Review and Difix Label ). Patient was hospitalized.

7005116-1 | Bronchospasm, Dyspnoea, Pain In Extremity
Patient was taking Zaditen (View Usage). Patient had the following side effects: bronchospasm, dyspnoea, pain in extremity on Sep 13, 2010 from UKRAINE Additional patient health information: Female patient , 70 years of age, . Zaditen dosage: Unk.

6914902-5 | Abnormal Behaviour, Memory Impairment
Adverse event was reported on Jul 26, 2010 by a Male patient taking Zaditen (View Usage) (Dosage: 0.7 G, Bid) was diagnosed with otitis media and. Location: JAPAN , weighting 44.09 lb, After Zaditen was administered, patient had the following side effects: abnormal behaviour, memory impairment. During the same period patient was treated with CLAVAMOX (1.515 Mg, Bid) (View Clavamox Review and Clavamox Label ), BIOLACTIS (3 G) (View Biolactis Review and Biolactis Label ), MUCODYNE (1.2 G) (View Mucodyne Review and Mucodyne Label ).

6835541-0 | Supraventricular Extrasystoles
on Jul 06, 2010 Female patient from JAPAN , 24 years of age, was diagnosed with hypersensitivity and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: supraventricular extrasystoles. Zaditen dosage: .


6826322-2 | Supraventricular Extrasystoles
on Jul 06, 2010 Female patient from JAPAN , 24 years of age, was diagnosed with hypersensitivity and was treated with Zaditen (View Usage). Patient had the following side effects: supraventricular extrasystoles. Zaditen dosage: .

6819798-8 | Abnormal Behaviour
Patient was taking Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: abnormal behaviour on Jun 23, 2010 from JAPAN Additional patient health information: Male patient , child 5 years of age, was diagnosed with otitis media and. Zaditen dosage: Unk. During the same period patient was treated with CLAVAMOX (Unk) (View Clavamox Review and Clavamox Label ).

6800913-7 | Condition Aggravated, Erythema Multiforme, Pyrexia
Adverse event was reported on Jun 16, 2010 by a Male patient taking Zaditen (View Usage) (Dosage: 0.45 Mg, Bid) was diagnosed with hypersensitivity, otitis media acute and. Location: JAPAN , child 3 years of age, Patient experienced the following unwanted or unexpected effects: condition aggravated, erythema multiforme, pyrexia. During the same period patient was treated with TRANSAMIN (0.4 Mg) (View Transamin Review and Transamin Label ), ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ), ANTIALLERGIC AGENTS, EXCL CORTICOSTEROIDS (View Antiallergic Agents, Excl Corticosteroids Review and Antiallergic Agents, Excl Corticosteroids Label ), ALPINYL (100 Mg) (View Alpinyl Review and Alpinyl Label ), WIDECILLIN (0.93 G, Tid) (View Widecillin Review and Widecillin Label ), BIOFERMIN (0.56 G, Tid) (View Biofermin Review and Biofermin Label ). Patient was hospitalized.

6794997-2 | Cystitis, Haematuria
on Jun 10, 2010 Male patient from JAPAN , child 3 years of age, was treated with Zaditen (View Usage). Patient had the following side effects: cystitis, haematuria. Zaditen dosage: .

6763531-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, Platelet Count Decreased, Rash, Zinc Sulphate Turbidity Increased
on May 27, 2010 Female patient from JAPAN , child 11 years of age, was diagnosed with rhinitis allergic, hypersensitivity and was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, hepatic enzyme increased, platelet count decreased, rash (What is rash?), zinc sulphate turbidity increased. Zaditen dosage: 2.0 G Daily. During the same period patient was treated with ANYRUME (2.4 Mg) (View Anyrume Review and Anyrume Label ), ALESION (Unk) (View Alesion Review and Alesion Label ).

6754169-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, Platelet Count Decreased, Rash, Zinc Sulphate Turbidity Increased
Patient was taking Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, hepatic enzyme increased, platelet count decreased, rash (What is rash?), zinc sulphate turbidity increased on May 20, 2010 from JAPAN Additional patient health information: Female patient , child 11 years of age, was diagnosed with rhinitis allergic and. Zaditen dosage: 2.0 G Daily. During the same period patient was treated with ANYRUME (2.4 Mg) (View Anyrume Review and Anyrume Label ).

6751055-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, Platelet Count Decreased, Rash, Zinc Sulphate Turbidity Increased
Adverse event was reported on May 20, 2010 by a Female patient taking Zaditen (View Usage) (Dosage: 2.0 G Daily) was diagnosed with rhinitis allergic and. Location: JAPAN , child 11 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, hepatic enzyme increased, platelet count decreased, rash (What is rash?), zinc sulphate turbidity increased. During the same period patient was treated with ANYRUME (2.4 Mg) (View Anyrume Review and Anyrume Label ).

6731989-3 | Migraine With Aura, Visual Acuity Reduced
on May 07, 2010 Male patient from AUSTRALIA , 13 years of age, was diagnosed with conjunctivitis allergic and was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: migraine with aura, visual acuity reduced. Zaditen dosage: Unk.

6723658-0 | Cystitis, Haematuria
on May 11, 2010 Male patient from JAPAN , child 3 years of age, was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: cystitis, haematuria. Zaditen dosage: .

6699953-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Hepatic Enzyme Increased, Platelet Count Decreased, Rash, Viral Infection
Patient was taking Zaditen (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, hepatic enzyme increased, platelet count decreased, rash (What is rash?), viral infection (What is viral infection?) on Apr 19, 2010 from JAPAN Additional patient health information: Female patient , child 11 years of age, was diagnosed with rhinitis allergic and. Zaditen dosage: 2.0 G Daily. During the same period patient was treated with ANYRUME (2.4 Mg) (View Anyrume Review and Anyrume Label ).

6650311-4 | Abnormal Behaviour, Atonic Seizures, Convulsion, Gaze Palsy, Restlessness, Syncope
Adverse event was reported on Mar 16, 2010 by a Male patient taking Zaditen (View Usage) (Dosage: Daily) was diagnosed with dermatitis atopic and. Location: JAPAN , child 7 years of age, After Zaditen was administered, patient had the following side effects: abnormal behaviour, atonic seizures, convulsion, gaze palsy, restlessness, syncope. Patient was hospitalized.

6648063-7 | Abnormal Behaviour, Atonic Seizures, Convulsion, Frontal Lobe Epilepsy, Gaze Palsy, Restlessness, Syncope, Upper Respiratory Tract Infection
on Mar 16, 2010 Male patient from JAPAN , child 7 years of age, was diagnosed with dermatitis atopic and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, atonic seizures, convulsion, frontal lobe epilepsy, gaze palsy, restlessness, syncope, upper respiratory tract infection. Zaditen dosage: Daily. Patient was hospitalized.

6623805-5 | Alanine Aminotransferase Increased, Blood Bilirubin Increased, Hepatitis Acute
on Feb 25, 2010 Female patient from ITALY , 48 years of age, was diagnosed with asthma (What is asthma?) and was treated with Zaditen (View Usage). Patient had the following side effects: alanine aminotransferase increased, blood bilirubin increased, hepatitis acute. Zaditen dosage: Unk. During the same period patient was treated with DIFIX (Unk) (View Difix Review and Difix Label ). Patient was hospitalized.

6614100-9 | Abnormal Behaviour, Atonic Seizures, Convulsion, Frontal Lobe Epilepsy, Gaze Palsy, Restlessness, Syncope, Upper Respiratory Tract Infection
Patient was taking Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: abnormal behaviour, atonic seizures, convulsion, frontal lobe epilepsy, gaze palsy, restlessness, syncope, upper respiratory tract infection on Feb 22, 2010 from JAPAN Additional patient health information: Male patient , child 7 years of age, was diagnosed with dermatitis atopic and. Zaditen dosage: Daily. Patient was hospitalized.

6611531-8 | Cough, Dysuria, Incorrect Dose Administered
Adverse event was reported on Feb 19, 2010 by a Male patient taking Zaditen (View Usage) (Dosage: Unk) . Location: JAPAN , child 4 years of age, Patient experienced the following unwanted or unexpected effects: cough, dysuria, incorrect dose administered. During the same period patient was treated with ONON (Unk) (View Onon Review and Onon Label ), NIPOLAZIN (Unk) (View Nipolazin Review and Nipolazin Label ). Patient was hospitalized.

6606512-4 | Abdominal Distension, Blister, Obstruction, Oedema Peripheral
on Feb 22, 2010 Male patient from BRAZIL , 82 years of age, was diagnosed with dermatitis and was treated with Zaditen (View Usage). Patient had the following side effects: abdominal distension, blister, obstruction, oedema peripheral. Zaditen dosage: 1 Mg, Bid. During the same period patient was treated with ALLEGRA (1 Tablet Daily) (View Allegra Review and Allegra Label ).

6599284-3 | Convulsion
on Feb 10, 2010 Male patient from JAPAN , child 7 years of age, was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: convulsion. Zaditen dosage: Unk. Patient was hospitalized.

6565454-3 | Cough, Dysuria, Incorrect Dose Administered
Patient was taking Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: cough, dysuria, incorrect dose administered on Jan 26, 2010 from JAPAN Additional patient health information: Male patient , child 4 years of age, . Zaditen dosage: . Patient was hospitalized.

6460062-7 | Nasopharyngitis
Adverse event was reported on Nov 20, 2009 by a Male patient taking Zaditen (View Usage) (Dosage: 2 Mg, Daily) was diagnosed with rhinitis allergic and. Location: JAPAN , child 12 years of age, Patient had the following side effects: nasopharyngitis.

6446459-X | Asthma
on Nov 12, 2009 Male patient from JAPAN , child 12 years of age, was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: asthma (What is asthma?). Zaditen dosage: Unk.

6413218-3 | Abdominal Distension, Blister, Obstruction, Oedema Peripheral
on Oct 15, 2009 Male patient from BRAZIL , 82 years of age, was diagnosed with dermatitis and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension, blister, obstruction, oedema peripheral. Zaditen dosage: 1 Mg, Bid. During the same period patient was treated with ALLEGRA (1 Tablet Daily) (View Allegra Review and Allegra Label ).

6401384-5 | Convulsion
Patient was taking Zaditen (View Usage). Patient had the following side effects: convulsion on Oct 05, 2009 from JAPAN Additional patient health information: Male patient , child 2 years of age, was diagnosed with rhinorrhoea and. Zaditen dosage: Unk. During the same period patient was treated with FLOMOX (Unk) (View Flomox Review and Flomox Label ), CALONAL (Unk) (View Calonal Review and Calonal Label ).

6389212-8 | Abdominal Distension, Blister, Obstruction, Oedema Peripheral
Adverse event was reported on Sep 23, 2009 by a Male patient taking Zaditen (View Usage) (Dosage: 1 Mg, Bid) was diagnosed with dermatitis and. Location: BRAZIL , 82 years of age, After Zaditen was administered, patient had the following side effects: abdominal distension, blister, obstruction, oedema peripheral. During the same period patient was treated with ALLEGRA (1 Tablet Daily) (View Allegra Review and Allegra Label ).

6347938-6 | Abnormal Behaviour, Convulsion
on Sep 04, 2009 Female patient from JAPAN , child 7 years of age, was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, convulsion. Zaditen dosage: Unk.

6334550-8 | Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Biopsy Liver, Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Liver Disorder, Pyrexia
on Aug 18, 2009 Female patient from JAPAN , weighting 141.1 lb, was diagnosed with seasonal allergy and was treated with Zaditen (View Usage). Patient had the following side effects: alanine aminotransferase increased, arthralgia, aspartate aminotransferase increased, biopsy liver, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, liver disorder, pyrexia. Zaditen dosage: Unk. During the same period patient was treated with PSEUDOEPHEDRINE HCL (Unk) (View Pseudoephedrine Hcl Review and Pseudoephedrine Hcl Label ). Patient was hospitalized.

6301095-0 | Haematuria
Patient was taking Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: haematuria on Jul 27, 2009 from JAPAN Additional patient health information: Male patient , 36 years of age, was diagnosed with rhinorrhoea, cough and. Zaditen dosage: 2 Mg Daily. During the same period patient was treated with LENDORMIN (View Lendormin Review and Lendormin Label ), SOLANAX (View Solanax Review and Solanax Label ), BISOLVON (View Bisolvon Review and Bisolvon Label ), BERIZYM (View Berizym Review and Berizym Label ).

6290651-4 | Arthralgia, Arthropathy, Asthenia, Balance Disorder, Blood Pressure Increased, Feeling Drunk, Headache, Osteoarthritis, Sedation
Adverse event was reported on Jul 16, 2009 by a Female patient taking Zaditen (View Usage) (Dosage: 2 Mg, 1 Tablet At Night) was diagnosed with dermatitis allergic, osteoarthritis (What is osteoarthritis?), hypertension and. Location: BRAZIL , weighting 154.3 lb, Patient experienced the following unwanted or unexpected effects: arthralgia, arthropathy, asthenia, balance disorder, blood pressure increased, feeling drunk, headache (What is headache?), osteoarthritis (What is osteoarthritis?), sedation. During the same period patient was treated with LOVAZA (4 Capsules Daily) (View Lovaza Review and Lovaza Label ), ACECLOFENAC (100 Mg, Unk) (View Aceclofenac Review and Aceclofenac Label ), NIMESULIDE (100 Mg, Unk) (View Nimesulide Review and Nimesulide Label ), FAMOTIDINE (20 Mg, Unk) (View Famotidine Review and Famotidine Label ), SERTRALINE (50 Mg, Unk) (View Sertraline Review and Sertraline Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (1 Capsule Daily) (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ).

6263763-9 | Agranulocytosis, C-reactive Protein Increased, Fatigue, Haemophilus Infection, Lung Infiltration, Mood Altered, Nasopharyngitis, Neutrophil Count Decreased, Pneumonia
on Jul 03, 2009 Male patient from JAPAN , weighting 14.77 lb, was diagnosed with urticaria, eczema (What is eczema?) and was treated with Zaditen (View Usage). Patient had the following side effects: agranulocytosis, c-reactive protein increased, fatigue, haemophilus infection, lung infiltration, mood altered, nasopharyngitis, neutrophil count decreased, pneumonia (What is pneumonia?). Zaditen dosage: Unk. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6258322-8 | Haematuria
on Jun 29, 2009 Male patient from JAPAN , 36 years of age, was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: haematuria. Zaditen dosage: .

6248339-1 | Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Biopsy Liver, Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Liver Disorder, Pyrexia
Patient was taking Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, arthralgia, aspartate aminotransferase increased, biopsy liver, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, liver disorder, pyrexia on Jun 19, 2009 from JAPAN Additional patient health information: Female patient , weighting 141.1 lb, was diagnosed with seasonal allergy and. Zaditen dosage: Unk. During the same period patient was treated with PSEUDOEPHEDRINE HCL (Unk) (View Pseudoephedrine Hcl Review and Pseudoephedrine Hcl Label ). Patient was hospitalized.

6234056-0 | Dizziness, Dyspnoea, Gastrointestinal Disorder, Hypotonia, Loss Of Consciousness, Nausea
Adverse event was reported on May 27, 2009 by a Female patient taking Zaditen (View Usage) (Dosage: Unk) was diagnosed with conjunctivitis allergic and. Location: RUSSIAN FEDERATION , 37 years of age, Patient had the following side effects: dizziness (What is dizziness?), dyspnoea, gastrointestinal disorder, hypotonia, loss of consciousness, nausea (What is nausea?).

6228524-5 | Agranulocytosis, C-reactive Protein Increased, Fatigue, Haemophilus Infection, Lung Infiltration, Mood Altered, Nasopharyngitis, Neutrophil Count Decreased, Pneumonia
on Jun 02, 2009 Male patient from JAPAN , weighting 14.77 lb, was diagnosed with urticaria, eczema (What is eczema?) and was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: agranulocytosis, c-reactive protein increased, fatigue, haemophilus infection, lung infiltration, mood altered, nasopharyngitis, neutrophil count decreased, pneumonia (What is pneumonia?). Zaditen dosage: Unk. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6228262-9 | Syncope
on Jun 03, 2009 Female patient from FINLAND , child 10 years of age, was diagnosed with hypersensitivity and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: syncope. Zaditen dosage: .

6227615-2 | Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Biopsy Liver, Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Liver Disorder, Pyrexia
Patient was taking Zaditen (View Usage). Patient had the following side effects: alanine aminotransferase increased, arthralgia, aspartate aminotransferase increased, biopsy liver, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, liver disorder, pyrexia on Jun 01, 2009 from JAPAN Additional patient health information: Female patient , weighting 141.1 lb, was diagnosed with seasonal allergy and. Zaditen dosage: Unk. During the same period patient was treated with PSEUDOEPHEDRINE HCL (Unk) (View Pseudoephedrine Hcl Review and Pseudoephedrine Hcl Label ). Patient was hospitalized.

6198482-0 | Liver Disorder
Adverse event was reported on May 13, 2009 by a Female patient taking Zaditen (View Usage) (Dosage: Unk) . Location: JAPAN , 50 years of age, After Zaditen was administered, patient had the following side effects: liver disorder. Patient was hospitalized.

6193944-4 | Erythema, Face Oedema, Pruritus, Skin Exfoliation
on May 07, 2009 Female patient from JAPAN , 53 years of age, was diagnosed with seasonal allergy and was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, face oedema, pruritus, skin exfoliation. Zaditen dosage: 1 Df/day.

6173715-5 | Nervousness, Tachycardia
on Apr 22, 2009 Female patient from SPAIN , 46 years of age, was diagnosed with hypersensitivity and was treated with Zaditen (View Usage). Patient had the following side effects: nervousness, tachycardia. Zaditen dosage: Unk.

6172401-5 | Accidental Overdose, Hypersomnia, Vomiting
Patient was taking Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: accidental overdose, hypersomnia, vomiting on Apr 21, 2009 from JAPAN Additional patient health information: Female patient , child 3 years of age, weighting 22.05 lb, was diagnosed with rhinitis and. Zaditen dosage: 4.5 Mg. Patient was hospitalized.

6045566-3 | Accidental Overdose, Somnolence
Adverse event was reported on Feb 26, 2008 by a Female patient taking Zaditen (View Usage) (Dosage: 2 Capsules, Once) was diagnosed with seasonal allergy and. Location: JAPAN , 42 years of age, Patient experienced the following unwanted or unexpected effects: accidental overdose, somnolence.

5978809-2 | Arrhythmia, Bradycardia
on Nov 26, 2008 Female patient from JAPAN , 77 years of age, was treated with Zaditen (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), bradycardia. Zaditen dosage: 4 Mg, Bid.

5940982-X | Arrhythmia, Bradycardia
on Oct 28, 2008 Female patient from JAPAN , 77 years of age, was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: arrhythmia (What is arrhythmia?), bradycardia. Zaditen dosage: 4 Mg, Bid.

5940966-1 | Gamma-glutamyltransferase Increased
Patient was taking Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: gamma-glutamyltransferase increased on Oct 27, 2008 from GREECE Additional patient health information: Female patient , 38 years of age, . Zaditen dosage: 1 Mg.

5908780-0 | Eczema, Erythema Multiforme, Eye Swelling, Impetigo, Pyrexia, Rash Papular, Skin Exfoliation, Staphylococcal Infection
Adverse event was reported on Sep 26, 2008 by a Male patient taking Zaditen (View Usage) (Dosage: Unk) was diagnosed with dermatitis allergic, pruritus, rash (What is rash?) and. Location: JAPAN , weighting 19.84 lb, Patient had the following side effects: eczema (What is eczema?), erythema multiforme, eye swelling, impetigo (What is impetigo?), pyrexia, rash papular, skin exfoliation, staphylococcal infection (What is staphylococcal infection?). During the same period patient was treated with CELTECT (0.5g) (View Celtect Review and Celtect Label ), STADERM (Unk) (View Staderm Review and Staderm Label ).

5899588-3 | Erythema Multiforme, Eye Swelling, Stevens-johnson Syndrome
on Sep 19, 2008 Male patient from JAPAN , child 1 years of age, was treated with Zaditen (View Usage). After Zaditen was administered, patient had the following side effects: erythema multiforme, eye swelling, stevens-johnson syndrome. Zaditen dosage: Unk. During the same period patient was treated with STADERM (View Staderm Review and Staderm Label ).

5874541-4 | Erythema Multiforme, Eye Swelling, Stevens-johnson Syndrome
on Sep 01, 2008 Male patient from JAPAN , child 1 years of age, was treated with Zaditen (View Usage). Patient experienced the following unwanted or unexpected effects: erythema multiforme, eye swelling, stevens-johnson syndrome. Zaditen dosage: Unk.

5866295-2 | Accidental Overdose, Somnolence
Patient was taking Zaditen (View Usage). Patient had the following side effects: accidental overdose, somnolence on Aug 21, 2008 from JAPAN Additional patient health information: Male patient , 26 years of age, was diagnosed with rhinorrhoea and. Zaditen dosage: Unk.

Showing 1-50 of 150  Next Page  >


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Zaditen Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

hamed   Iran

12:45pm on Friday, April 15th, 2011

I wanna know that what is the exact effect of the zaditen pomade on children(boy)under one yrs old?

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 Zaditen 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 Zaditen quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Zaditen 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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Zaditen Reactions
Abnormal Behaviour
Accidental Overdose
Alanine Aminotransferase Increased
Arthralgia
Aspartate Aminotransferase Increased
AsthmaWhat is Asthma?
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Cholesterol Increased
Blood Glucose Increased
Blood Lactate Dehydrogenase Increased
Blood Pressure Decreased
Blood Pressure Increased
Convulsion
Depressed Level Of Consciousness
Erythema Multiforme
Febrile Convulsion
Gamma-glutamyltransferase Increased
Gaze Palsy
Haematuria
HeadacheWhat is Headache?
Liver Disorder
Loss Of Consciousness
Nasopharyngitis
Pallor
Platelet Count Decreased
PneumoniaWhat is Pneumonia?
Pyrexia
Somnolence
Syncope
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