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Zelitrex adverse events reported to FDA.

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Summary

FDA Adverse Reports: 161. View All

Zelitrex FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 102

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

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6943923-1 | Tachycardia
on Aug 18, 2010 Female patient from FRANCE , 51 years of age, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: tachycardia. Zelitrex dosage: 1g Three Times Per Day. During the same period patient was treated with XELODA (View Xeloda Review and Xeloda Label ). Patient was hospitalized.

6820071-2 | Macrocytosis
Patient was taking Zelitrex (View Usage). Patient had the following side effects: macrocytosis on Jun 28, 2010 from FRANCE Additional patient health information: Female patient , 50 years of age, was diagnosed with prophylaxis and. Zelitrex dosage: 1tab Every 3 Days.

6779634-5 | Erythema Multiforme
Adverse event was reported on Jun 10, 2010 by a Female patient taking Zelitrex (View Usage) (Dosage: 500mg Twice Per Day) was diagnosed with oral herpes and. Location: FRANCE , 66 years of age, weighting 143.3 lb, After Zelitrex was administered, patient had the following side effects: erythema multiforme.

6756500-2 | Anaemia Macrocytic, Renal Failure
on May 26, 2010 Female patient from BELGIUM , weighting 125.7 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia macrocytic, renal failure. Zelitrex dosage: 500mg Six Times Per Day. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), COVERSYL (View Coversyl Review and Coversyl Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), FOSAVANCE (View Fosavance Review and Fosavance Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), LASIX (View Lasix Review and Lasix Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ).


6754014-7 | Erythema Multiforme
on May 27, 2010 Female patient from FRANCE , 66 years of age, was diagnosed with oral herpes and was treated with Zelitrex (View Usage). Patient had the following side effects: erythema multiforme. Zelitrex dosage: 500mg Per Day.

6726393-8 | Hallucination, Olfactory, Sinus Polyp
Patient was taking Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: hallucination, olfactory, sinus polyp on May 07, 2010 from FRANCE Additional patient health information: Male patient , 62 years of age, was diagnosed with antiviral prophylaxis, osteoporosis (What is osteoporosis?) and. Zelitrex dosage: .5tab Twice Per Day. During the same period patient was treated with FOSAMAX (View Fosamax Review and Fosamax Label ).

6658161-X | Blepharitis, Cheilitis, Conjunctivitis, Dermatitis Bullous, Diarrhoea, Inflammation, Iron Deficiency, Nikolsky's Sign
Adverse event was reported on Mar 29, 2010 by a Female patient taking Zelitrex (View Usage) (Dosage: 500mg Twice Per Day) . Location: FRANCE , weighting 121.3 lb, Patient experienced the following unwanted or unexpected effects: blepharitis, cheilitis, conjunctivitis, dermatitis bullous, diarrhoea, inflammation, iron deficiency, nikolsky's sign. During the same period patient was treated with TRIFLUCAN (50mg Per Day) (View Triflucan Review and Triflucan Label ), TOLEXINE (1unit Per Day) (View Tolexine Review and Tolexine Label ), ATARAX (25mg Per Day) (View Atarax Review and Atarax Label ), LACTOBACILLUS (View Lactobacillus Review and Lactobacillus Label ), BETADINE (View Betadine Review and Betadine Label ). Patient was hospitalized.

6656084-3 | Blood Creatinine Increased, Confusional State, Constipation, Coordination Abnormal, Delirium, Dysarthria, Dysphagia, Erythema, Hallucination
on Mar 19, 2010 Female patient from NETHERLANDS , weighting 176.4 lb, was diagnosed with herpes zoster and was treated with Zelitrex (View Usage). Patient had the following side effects: blood creatinine increased, confusional state, constipation (What is constipation?), coordination abnormal, delirium, dysarthria, dysphagia, erythema, hallucination. Zelitrex dosage: 500mg Four Times Per Day. During the same period patient was treated with RENAGEL (800mg Twice Per Day) (View Renagel Review and Renagel Label ), ADALAT (60mg Per Day) (View Adalat Review and Adalat Label ), METOPROLOL (100mg Per Day) (View Metoprolol Review and Metoprolol Label ), LIPITOR (40mg Per Day) (View Lipitor Review and Lipitor Label ), ASCAL CARDIO (100mg Per Day) (View Ascal Cardio Review and Ascal Cardio Label ), PLAVIX (75mg Per Day) (View Plavix Review and Plavix Label ), ALLOPURINOL (100mg Per Day) (View Allopurinol Review and Allopurinol Label ), TRITACE (10mg Per Day) (View Tritace Review and Tritace Label ). Patient was hospitalized.

6590682-0 | Accidental Overdose, Agitation, Coma, Confusional State, Hypertonia, Myoclonus
on Feb 11, 2010 Male patient from FRANCE , 80 years of age, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: accidental overdose, agitation, coma, confusional state, hypertonia, myoclonus. Zelitrex dosage: 1g Three Times Per Day. During the same period patient was treated with RENAGEL (View Renagel Review and Renagel Label ), ROCALTROL (View Rocaltrol Review and Rocaltrol Label ), ATARAX (View Atarax Review and Atarax Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), KAYEXALATE (View Kayexalate Review and Kayexalate Label ), LASILIX (View Lasilix Review and Lasilix Label ). Patient was hospitalized.

6583278-8 | Blepharitis, Cheilitis, Conjunctivitis, Dermatitis Bullous, Diarrhoea, Inflammation, Iron Deficiency, Nikolsky's Sign
Patient was taking Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: blepharitis, cheilitis, conjunctivitis, dermatitis bullous, diarrhoea, inflammation, iron deficiency, nikolsky's sign on Feb 08, 2010 from FRANCE Additional patient health information: Female patient , weighting 121.3 lb, . Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with TRIFLUCAN (50mg Per Day) (View Triflucan Review and Triflucan Label ), TOLEXINE (1unit Per Day) (View Tolexine Review and Tolexine Label ), ATARAX (25mg Per Day) (View Atarax Review and Atarax Label ), LACTOBACILLUS (View Lactobacillus Review and Lactobacillus Label ), BETADINE (View Betadine Review and Betadine Label ). Patient was hospitalized.

6461048-9 | Areflexia, Balance Disorder, Blood Immunoglobulin M Increased, Dysstasia, Hypogammaglobulinaemia, Off Label Use, Pain In Extremity, Paraesthesia, Peripheral Sensory Neuropathy
Adverse event was reported on Nov 19, 2009 by a Female patient taking Zelitrex (View Usage) (Dosage: 500mg Twice Per Day) was diagnosed with antiviral prophylaxis, hypothyroidism, cerebrovascular accident and. Location: FRANCE , weighting 147.7 lb, Patient had the following side effects: areflexia, balance disorder, blood immunoglobulin m increased, dysstasia, hypogammaglobulinaemia, off label use, pain in extremity, paraesthesia, peripheral sensory neuropathy. During the same period patient was treated with LEVOTHYROXINE SODIUM (50mcg Per Day) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), CRESTOR (5mg Per Day) (View Crestor Review and Crestor Label ), KARDEGIC 160 (160mg Per Day) (View Kardegic 160 Review and Kardegic 160 Label ). Patient was hospitalized.

6443152-4 | Balance Disorder, Communication Disorder, Confusional State, Disorientation, Dizziness, Dysstasia, Fall, Fatigue, Gait Disturbance
on Nov 09, 2009 Female patient from FRANCE , weighting 88.18 lb, was diagnosed with herpes zoster, hypertension, constipation (What is constipation?) and was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: balance disorder, communication disorder, confusional state, disorientation, dizziness (What is dizziness?), dysstasia, fall (What is fall?), fatigue, gait disturbance. Zelitrex dosage: 1000mg Twice Per Day. During the same period patient was treated with DILTIAZEM (200mg Per Day) (View Diltiazem Review and Diltiazem Label ), AERIUS (5mg Per Day) (View Aerius Review and Aerius Label ), KARDEGIC (75mg Per Day) (View Kardegic Review and Kardegic Label ), LACTULOSE (10g Twice Per Day) (View Lactulose Review and Lactulose Label ), OMEPRAZOLE (10mg Per Day) (View Omeprazole Review and Omeprazole Label ).

6441504-X | Blood Pressure Increased, Crystalluria, Hyperkalaemia, Oedema Peripheral, Off Label Use, Renal Failure Acute
on Nov 06, 2009 Male patient from FRANCE , 67 years of age, weighting 169.8 lb, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, crystalluria, hyperkalaemia, oedema peripheral, off label use, renal failure acute. Zelitrex dosage: 1g Three Times Per Day. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), COAPROVEL (View Coaprovel Review and Coaprovel Label ), MANIDIPINE HYDROCHLORIDE (View Manidipine Hydrochloride Review and Manidipine Hydrochloride Label ), IKOREL (View Ikorel Review and Ikorel Label ), NOVONORM (View Novonorm Review and Novonorm Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), TAHOR (View Tahor Review and Tahor Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6423450-0 | Neuropathy Peripheral, Off Label Use
Patient was taking Zelitrex (View Usage). Patient had the following side effects: neuropathy peripheral, off label use on Oct 21, 2009 from FRANCE Additional patient health information: Female patient , 65 years of age, was diagnosed with antiviral prophylaxis and. Zelitrex dosage: 500mg Twice Per Day.

6368512-1 | Angina Unstable, Blood Lactate Dehydrogenase Increased, Eosinophilia, Hepatocellular Injury, Leukocytosis, Lymphadenopathy, Obesity
Adverse event was reported on Sep 11, 2009 by a Male patient taking Zelitrex (View Usage) (Dosage: 1g Three Times Per Day) was diagnosed with herpes ophthalmic and. Location: FRANCE , weighting 158.7 lb, After Zelitrex was administered, patient had the following side effects: angina unstable, blood lactate dehydrogenase increased, eosinophilia, hepatocellular injury, leukocytosis, lymphadenopathy, obesity (What is obesity?). During the same period patient was treated with TAVANIC (View Tavanic Review and Tavanic Label ), TOBRADEX (View Tobradex Review and Tobradex Label ). Patient was hospitalized.

6349319-8 | Cerebellar Syndrome
on Sep 03, 2009 Male patient from FRANCE , 80 years of age, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: cerebellar syndrome. Zelitrex dosage: 500mg See Dosage Text. Patient was hospitalized.

6314990-3 | Ageusia, Alopecia, Anosmia, Disturbance In Attention, Dry Mouth, Dysarthria, Nausea, Poor Quality Sleep
on Aug 11, 2009 Female patient from NETHERLANDS , 73 years of age, was diagnosed with herpes virus infection and was treated with Zelitrex (View Usage). Patient had the following side effects: ageusia, alopecia, anosmia, disturbance in attention, dry mouth, dysarthria, nausea (What is nausea?), poor quality sleep. Zelitrex dosage: .

6129756-7 | Aphasia, Confusional State, Disorientation, Dysarthria, Gait Disturbance, Hallucination, Renal Failure Acute
Patient was taking Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: aphasia (What is aphasia?), confusional state, disorientation, dysarthria, gait disturbance, hallucination, renal failure acute on Mar 18, 2009 from FRANCE Additional patient health information: Female patient , 78 years of age, was diagnosed with herpes ophthalmic and. Zelitrex dosage: 1000mg Three Times Per Day. During the same period patient was treated with COTAREG (View Cotareg Review and Cotareg Label ), ZOCOR (10mg Per Day) (View Zocor Review and Zocor Label ), CACIT VITAMINE D3 (View Cacit Vitamine D3 Review and Cacit Vitamine D3 Label ), PARIET (10mg Per Day) (View Pariet Review and Pariet Label ). Patient was hospitalized.

6126166-3 | Blister, Epidermolysis, Mucosal Inflammation, Pyrexia, Rash, Skin Exfoliation, Stomatitis, Toxic Epidermal Necrolysis
Adverse event was reported on Mar 13, 2009 by a Male patient taking Zelitrex (View Usage) (Dosage: ) was diagnosed with prophylaxis, graft versus host disease, infection (What is infection?), dyspepsia, thrombophlebitis, hypertension and. Location: DENMARK , 36 years of age, Patient experienced the following unwanted or unexpected effects: blister, epidermolysis, mucosal inflammation, pyrexia, rash (What is rash?), skin exfoliation, stomatitis, toxic epidermal necrolysis. During the same period patient was treated with RAPAMUNE (1mg Per Day) (View Rapamune Review and Rapamune Label ), FURIX (View Furix Review and Furix Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ), VFEND (200mg Twice Per Day) (View Vfend Review and Vfend Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), DAPSON (View Dapson Review and Dapson Label ), INNOHEP (9000iu Per Day) (View Innohep Review and Innohep Label ), PLENDIL (View Plendil Review and Plendil Label ).

6094002-X | Menstrual Disorder, Syncope
on Feb 19, 2009 Female patient from FRANCE , 22 years of age, was diagnosed with herpes virus infection, contraception and was treated with Zelitrex (View Usage). Patient had the following side effects: menstrual disorder, syncope. Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with LEVONORGESTREL AND ETHINYL ESTRADIOL (View Levonorgestrel And Ethinyl Estradiol Review and Levonorgestrel And Ethinyl Estradiol Label ).

6055540-9 | Arthralgia, Hypoaesthesia, Pain
on Jan 19, 2009 Male patient from FRANCE , 64 years of age, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: arthralgia, hypoaesthesia, pain (What is pain?). Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with MABTHERA (375mgm2 Per Day) (View Mabthera Review and Mabthera Label ), FLUDARA (40mgm2 Cyclic) (View Fludara Review and Fludara Label ), BACTRIM DS (1tab Three Times Per Week) (View Bactrim Ds Review and Bactrim Ds Label ). Patient was hospitalized.

6051572-5 | Agranulocytosis, Prostatitis
Patient was taking Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: agranulocytosis, prostatitis on Jan 19, 2009 from FRANCE Additional patient health information: Male patient , 53 years of age, was diagnosed with hyperthyroidism and. Zelitrex dosage: . During the same period patient was treated with PROPYL THIOURACIL (6unit Per Day) (View Propyl-thiouracil Review and Propyl-thiouracil Label ), BACTRIM (1unit Per Day) (View Bactrim Review and Bactrim Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), ASPEGIC 325 (View Aspegic 325 Review and Aspegic 325 Label ), ATARAX (View Atarax Review and Atarax Label ), IMOVANE (View Imovane Review and Imovane Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), MAGNE B6 (View Magne B6 Review and Magne B6 Label ). Patient was hospitalized.

6038591-X | Erythema, Exfoliative Rash, Pruritus, Psoriasis, Skin Lesion
Adverse event was reported on Jan 09, 2009 by a Female patient taking Zelitrex (View Usage) (Dosage: 500mg Per Day) . Location: FRANCE , 69 years of age, weighting 141.1 lb, Patient had the following side effects: erythema, exfoliative rash, pruritus, psoriasis, skin lesion. During the same period patient was treated with TOBRADEX (1drop Twice Per Day) (View Tobradex Review and Tobradex Label ).

6000058-2 | Erythema, Exfoliative Rash, Pruritus, Psoriasis, Skin Lesion
on Dec 05, 2008 Female patient from FRANCE , 69 years of age, weighting 141.1 lb, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: erythema, exfoliative rash, pruritus, psoriasis, skin lesion. Zelitrex dosage: 500mg Per Day. During the same period patient was treated with TOBRADEX (1drop Twice Per Day) (View Tobradex Review and Tobradex Label ).

5963373-4 | Feeling Abnormal, Hallucination
on Nov 18, 2008 Female patient from FRANCE , 18 years of age, weighting 110.2 lb, was diagnosed with erythema multiforme and was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: feeling abnormal, hallucination. Zelitrex dosage: 1tab Per Day.

5961575-4 | Agitation, Confusional State, Disorientation, Disturbance In Attention, Hallucination, Mental Impairment, Overdose
Patient was taking Zelitrex (View Usage). Patient had the following side effects: agitation, confusional state, disorientation, disturbance in attention, hallucination, mental impairment, overdose on Nov 19, 2008 from FRANCE Additional patient health information: Male patient , 85 years of age, was diagnosed with herpes zoster ophthalmic and. Zelitrex dosage: 500mg Six Times Per Day. Patient was hospitalized.

5959851-4 | Blister, Epidermolysis, Pyrexia, Rash, Skin Exfoliation, Stomatitis, Toxic Epidermal Necrolysis
Adverse event was reported on Nov 17, 2008 by a Male patient taking Zelitrex (View Usage) (Dosage: ) was diagnosed with graft versus host disease, thrombophlebitis and. Location: DENMARK , 36 years of age, After Zelitrex was administered, patient had the following side effects: blister, epidermolysis, pyrexia, rash (What is rash?), skin exfoliation, stomatitis, toxic epidermal necrolysis. During the same period patient was treated with RAPAMUNE (1mg Per Day) (View Rapamune Review and Rapamune Label ), FURIX (View Furix Review and Furix Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ), VFEND (View Vfend Review and Vfend Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), DAPSON (View Dapson Review and Dapson Label ), INNOHEP (9000iu Per Day) (View Innohep Review and Innohep Label ).

5959845-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Chills, Erythema, Gamma-glutamyltransferase Increased, Headache, Hepatitis Acute, Hepatocellular Injury
on Nov 17, 2008 Male patient from FRANCE , 53 years of age, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, chills, erythema, gamma-glutamyltransferase increased, headache (What is headache?), hepatitis acute, hepatocellular injury. Zelitrex dosage: . During the same period patient was treated with VELCADE (2.3mg Per Day) (View Velcade Review and Velcade Label ), DEXAMETHASONE TAB (20mg Cyclic) (View Dexamethasone Tab Review and Dexamethasone Tab Label ), BACTRIM (1tab Alternate Days) (View Bactrim Review and Bactrim Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5955064-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Chills, Erythema, Gamma-glutamyltransferase Increased, Headache, Hepatitis Acute, Hepatocellular Injury
on Nov 13, 2008 Male patient from FRANCE , 53 years of age, was treated with Zelitrex (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, chills, erythema, gamma-glutamyltransferase increased, headache (What is headache?), hepatitis acute, hepatocellular injury. Zelitrex dosage: . During the same period patient was treated with VELCADE (2.3mg Per Day) (View Velcade Review and Velcade Label ), DEXAMETHASONE 0.5MG TAB (20mg Cyclic) (View Dexamethasone 0.5mg Tab Review and Dexamethasone 0.5mg Tab Label ), BACTRIM (1tab Alternate Days) (View Bactrim Review and Bactrim Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5928079-6 | Feeling Abnormal, Hallucination
Patient was taking Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: feeling abnormal, hallucination on Oct 16, 2008 from FRANCE Additional patient health information: Female patient , 18 years of age, weighting 110.2 lb, was diagnosed with erythema multiforme and. Zelitrex dosage: 1tab Per Day.

5926628-5 | Aphthous Stomatitis, Eating Disorder, Mouth Ulceration, Quality Of Life Decreased
Adverse event was reported on Oct 13, 2008 by a Female patient taking Zelitrex (View Usage) (Dosage: ) was diagnosed with non-hodgkin's lymphoma and. Location: FRANCE , 56 years of age, Patient experienced the following unwanted or unexpected effects: aphthous stomatitis, eating disorder (What is eating disorder?), mouth ulceration, quality of life decreased. During the same period patient was treated with MABTHERA (375mgm2 Per Day) (View Mabthera Review and Mabthera Label ), PENTACARINAT (1unit Monthly) (View Pentacarinat Review and Pentacarinat Label ).

5920517-8 | Haematochezia, Haemorrhage
on Oct 09, 2008 Female patient from FRANCE , 66 years of age, was treated with Zelitrex (View Usage). Patient had the following side effects: haematochezia, haemorrhage. Zelitrex dosage: 1g Three Times Per Day.

5913903-3 | Anaemia
on Sep 29, 2008 Male patient from FRANCE , 40 years of age, was diagnosed with opportunistic infection prophylaxis, fungal infection (What is fungal infection?), hepatitis c positive and was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: anaemia. Zelitrex dosage: . During the same period patient was treated with PREZISTA (600mg Twice Per Day) (View Prezista Review and Prezista Label ), NORVIR (100mg Twice Per Day) (View Norvir Review and Norvir Label ), TRUVADA (View Truvada Review and Truvada Label ), TRIFLUCAN (View Triflucan Review and Triflucan Label ), PEGINTERFERON ALFA 2B (View Peginterferon Alfa-2b Review and Peginterferon Alfa-2b Label ), RIBAVIRIN (View Ribavirin Review and Ribavirin Label ).

5895260-4 | Leukopenia, Neutropenia, Overdose
Patient was taking Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: leukopenia, neutropenia, overdose on Sep 18, 2008 from DENMARK Additional patient health information: Male patient , 65 years of age, was diagnosed with herpes simplex (What is herpes simplex?) and. Zelitrex dosage: 1000mg Per Day.

5876501-6 | Condition Aggravated, Corneal Disorder, Corneal Oedema, Eye Pain, Fatigue, Keratitis Herpetic
Adverse event was reported on Sep 03, 2008 by a Female patient taking Zelitrex (View Usage) (Dosage: 1tab See Dosage Text) . Location: FRANCE , 17 years of age, Patient had the following side effects: condition aggravated, corneal disorder, corneal oedema, eye pain, fatigue, keratitis herpetic. Patient was hospitalized.

5856282-2 | Agranulocytosis, Neutrophil Count Decreased, Spinal Myelogram Abnormal
on Aug 19, 2008 Female patient from FRANCE , 50 years of age, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: agranulocytosis, neutrophil count decreased, spinal myelogram abnormal. Zelitrex dosage: 500mg Per Day. During the same period patient was treated with DEROXAT (View Deroxat Review and Deroxat Label ), BACTRIM DS (3tab Weekly) (View Bactrim Ds Review and Bactrim Ds Label ), NOCTAMIDE (.5unit Per Day) (View Noctamide Review and Noctamide Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), LEDERFOLINE (View Lederfoline Review and Lederfoline Label ). Patient was hospitalized.

5848211-2 | Angioedema, Depressed Level Of Consciousness, Dizziness, Malaise, Pruritus
on Aug 05, 2008 Female patient from BELGIUM , 50 years of age, was diagnosed with genital herpes and was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, depressed level of consciousness, dizziness (What is dizziness?), malaise, pruritus. Zelitrex dosage: 500mg Single Dose.

5832311-7 | Altered State Of Consciousness, C-reactive Protein Increased, Clonus, Computerised Tomogram Abnormal, Confusional State, Csf Glucose Decreased, Disorientation, Leukoencephalopathy, Nuclear Magnetic Resonance Imaging Abnormal
Patient was taking Zelitrex (View Usage). Patient had the following side effects: altered state of consciousness, c-reactive protein increased, clonus, computerised tomogram abnormal, confusional state, csf glucose decreased, disorientation, leukoencephalopathy, nuclear magnetic resonance imaging abnormal on Jul 25, 2008 from FRANCE Additional patient health information: Female patient , 71 years of age, was diagnosed with herpes zoster and. Zelitrex dosage: 2tab Per Day. During the same period patient was treated with VELCADE (View Velcade Review and Velcade Label ), RIVOTRIL (View Rivotril Review and Rivotril Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), NORSET (View Norset Review and Norset Label ), NEORECORMON (View Neorecormon Review and Neorecormon Label ), ATARAX 25 (2tab Per Day) (View Atarax 25 Review and Atarax 25 Label ). Patient was hospitalized.

5762547-5 | Rash, Visual Acuity Reduced
Adverse event was reported on Jun 02, 2008 by a Male patient taking Zelitrex (View Usage) (Dosage: 500mg Three Times Per Day) . Location: NETHERLANDS , 61 years of age, After Zelitrex was administered, patient had the following side effects: rash (What is rash?), visual acuity reduced. During the same period patient was treated with NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), METOPROLOLTARTRAAT (100mg Per Day) (View Metoprololtartraat Review and Metoprololtartraat Label ).

5761187-1 | Keratitis Herpetic
on Jun 02, 2008 Female patient from FRANCE , 17 years of age, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: keratitis herpetic. Zelitrex dosage: 2tab Per Day. Patient was hospitalized.

5759793-3 | Alanine Aminotransferase Increased, Alpha 2 Globulin Increased, Anorexia, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Chromaturia, Cytolytic Hepatitis, Gamma-glutamyltransferase Increased
on May 29, 2008 Female patient from FRANCE , 73 years of age, was treated with Zelitrex (View Usage). Patient had the following side effects: alanine aminotransferase increased, alpha 2 globulin increased, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, chromaturia, cytolytic hepatitis, gamma-glutamyltransferase increased. Zelitrex dosage: . During the same period patient was treated with KENZEN (View Kenzen Review and Kenzen Label ), VITABACT (View Vitabact Review and Vitabact Label ). Patient was hospitalized.

5757095-2 | Stevens-johnson Syndrome
Patient was taking Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: stevens-johnson syndrome on May 27, 2008 from SOUTH AFRICA Additional patient health information: Male patient , 23 years of age, . Zelitrex dosage: . Patient was hospitalized.

5734880-4 | Blood Creatinine Increased, Constipation, Delirium, Dysarthria, Dysphagia, Incontinence, Oedema, Orthopnoea, Renal Failure Acute
Adverse event was reported on May 07, 2008 by a Female patient taking Zelitrex (View Usage) (Dosage: 500mg Four Times Per Day) was diagnosed with herpes zoster and. Location: NETHERLANDS , 83 years of age, weighting 176.4 lb, Patient experienced the following unwanted or unexpected effects: blood creatinine increased, constipation (What is constipation?), delirium, dysarthria, dysphagia, incontinence, oedema, orthopnoea, renal failure acute. During the same period patient was treated with RENAGEL (800mg Twice Per Day) (View Renagel Review and Renagel Label ), ADALAT (60mg Per Day) (View Adalat Review and Adalat Label ), METOPROLOL TARTRATE (100mg Per Day) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), LIPITOR (40mg Per Day) (View Lipitor Review and Lipitor Label ), ASCAL CARDIO (100mg Per Day) (View Ascal Cardio Review and Ascal Cardio Label ), PLAVIX (75mg Per Day) (View Plavix Review and Plavix Label ), ALLOPURINOL (100mg Per Day) (View Allopurinol Review and Allopurinol Label ), TRITACE (10mg Per Day) (View Tritace Review and Tritace Label ). Patient was hospitalized.

5730604-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased
on Apr 29, 2008 Female patient from FRANCE , 72 years of age, was diagnosed with genital herpes, sciatica (What is sciatica?) and was treated with Zelitrex (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyltransferase increased. Zelitrex dosage: 500mg Per Day. During the same period patient was treated with CLONAZEPAM (View Clonazepam Review and Clonazepam Label ).

5723566-8 | Blood Creatinine Increased, Hyperthermia, Protein Urine Present, Renal Failure Acute, Renal Tubular Disorder
on Apr 25, 2008 Male patient from FRANCE , 75 years of age, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: blood creatinine increased, hyperthermia, protein urine present, renal failure acute, renal tubular disorder. Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with BACTRIM DS (View Bactrim Ds Review and Bactrim Ds Label ), TEGELINE (View Tegeline Review and Tegeline Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), VFEND (View Vfend Review and Vfend Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), DAFLON (500mg Six Times Per Day) (View Daflon Review and Daflon Label ). Patient was hospitalized.

5709639-4 | Blood Creatinine Increased, Hyperthermia, Protein Urine Present, Renal Failure Acute, Renal Tubular Disorder
Patient was taking Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, hyperthermia, protein urine present, renal failure acute, renal tubular disorder on Apr 09, 2008 from FRANCE Additional patient health information: Male patient , 75 years of age, . Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ), TEGELINE (View Tegeline Review and Tegeline Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), VFEND (View Vfend Review and Vfend Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), DAFLON (500mg Six Times Per Day) (View Daflon Review and Daflon Label ). Patient was hospitalized.

5593316-7 | Chills, Eye Inflammation, Fatigue, Musculoskeletal Stiffness, Pyrexia, Rash Morbilliform, Serum Sickness
Adverse event was reported on Jan 10, 2008 by a Male patient taking Zelitrex (View Usage) (Dosage: ) . Location: FRANCE , 59 years of age, Patient had the following side effects: chills, eye inflammation, fatigue, musculoskeletal stiffness, pyrexia, rash morbilliform, serum sickness. During the same period patient was treated with ROCEPHIN (View Rocephin Review and Rocephin Label ). Patient was hospitalized.

5589731-8 | Angioedema, Hypotension, Urticaria
on Jan 08, 2008 Female patient from BELGIUM , 50 years of age, was treated with Zelitrex (View Usage). After Zelitrex was administered, patient had the following side effects: angioedema, hypotension, urticaria. Zelitrex dosage: 500mg Per Day. Patient was hospitalized.

5584288-X | Blood Lactate Dehydrogenase Increased, Haemolytic Anaemia, Haptoglobin Decreased
on Dec 31, 2007 Male patient from FRANCE , child 12 years of age, was treated with Zelitrex (View Usage). Patient experienced the following unwanted or unexpected effects: blood lactate dehydrogenase increased, haemolytic anaemia, haptoglobin decreased. Zelitrex dosage: 500mg Twice Per Day. During the same period patient was treated with ORACILLIN (500iu Twice Per Day) (View Oracillin Review and Oracillin Label ), FUNGIZONE (View Fungizone Review and Fungizone Label ), GARDENAL (View Gardenal Review and Gardenal Label ). Patient was hospitalized.

5580274-4 | Altered State Of Consciousness, Hallucination, Malaise, Overdose
Patient was taking Zelitrex (View Usage). Patient had the following side effects: altered state of consciousness, hallucination, malaise, overdose on Dec 24, 2007 from FRANCE Additional patient health information: Male patient , 86 years of age, weighting 198.4 lb, was diagnosed with herpes zoster and. Zelitrex dosage: 500mg Three Times Per Day. During the same period patient was treated with EPO (View Epo Review and Epo Label ), LASILIX (View Lasilix Review and Lasilix Label ), PRITOR (View Pritor Review and Pritor Label ), AMLOR (View Amlor Review and Amlor Label ). Patient was hospitalized.

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Zelitrex Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

scharlene   JOhannesburg

11:32am on Wednesday, August 24th, 2011

How long can one take zelitrex for as a prophlactic to prevent an outbreal of herpes 2? and at what ... read more »

wonderfulkba   Johannesburg

7:02pm on Sunday, November 15th, 2009

I have just realised I have been overdosing (two tablets instead of one tablet three time a day) for... read more »

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 Zelitrex 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 Zelitrex quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Zelitrex 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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Zelitrex Reactions
Abdominal PainWhat is Abdominal pain?
Abdominal Pain Upper
Agitation
Alanine Aminotransferase Increased
Anaemia
Aspartate Aminotransferase Increased
Balance Disorder
Blood Creatinine Increased
Chills
Confusional State
Diarrhoea
Disorientation
DizzinessWhat is Dizziness?
Dysarthria
Eosinophilia
Erythema
FallWhat is Fall?
Fatigue
Gamma-glutamyltransferase Increased
Hallucination
Hallucination, Visual
HeadacheWhat is Headache?
Leukopenia
NauseaWhat is Nausea?
Overdose
Pyrexia
Renal Failure Acute
Thrombocytopenia
Toxic Skin Eruption
Vomiting
Zelitrex 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 Zelitrex 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!