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Ternelin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 41. View All

Ternelin FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 20

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

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6171986-2 | Altered State Of Consciousness, Back Pain, Blood Pressure Decreased, Blood Pressure Increased, Headache, Hypotension, Somnolence, Spinal Compression Fracture
on Apr 22, 2009 Female patient from JAPAN , weighting 103.6 lb, was diagnosed with back pain (What is back pain?), hypertension, depression (What is depression?) and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: altered state of consciousness, back pain (What is back pain?), blood pressure decreased, blood pressure increased, headache (What is headache?), hypotension, somnolence, spinal compression fracture. Ternelin dosage: 2 Mg, Qd. During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ), FLUVOXAMINE MALEATE (25 Mg, Qd) (View Fluvoxamine Maleate Review and Fluvoxamine Maleate Label ), NATRIX (1 Mg, Qd) (View Natrix Review and Natrix Label ), LOXONIN (120 Mg) (View Loxonin Review and Loxonin Label ). Patient was hospitalized.

6162457-8 | Altered State Of Consciousness, Back Pain, Blood Pressure Decreased, Blood Pressure Increased, Somnolence, Spinal Compression Fracture
Patient was taking Ternelin (View Usage). Patient had the following side effects: altered state of consciousness, back pain (What is back pain?), blood pressure decreased, blood pressure increased, somnolence, spinal compression fracture on Apr 07, 2009 from JAPAN Additional patient health information: Female patient , weighting 103.6 lb, was diagnosed with back pain (What is back pain?), hypertension, depression (What is depression?), insomnia, hyperlipidaemia and. Ternelin dosage: 2 Mg, Qd. During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ), FLUVOXAMINE MALEATE (25 Mg, Qd) (View Fluvoxamine Maleate Review and Fluvoxamine Maleate Label ), NATRIX (1 Mg, Qd) (View Natrix Review and Natrix Label ), LOXONIN (120 Mg) (View Loxonin Review and Loxonin Label ), DIAZEPAM (5 Mg) (View Diazepam Review and Diazepam Label ), MEVALOTIN (10 Mg) (View Mevalotin Review and Mevalotin Label ). Patient was hospitalized.

6142749-9 | Glucose Urine Present, Glycosylated Haemoglobin Increased, Proteinuria
Adverse event was reported on Mar 26, 2009 by a Male patient taking Ternelin (View Usage) (Dosage: Unk) was diagnosed with diabetes mellitus and. Location: JAPAN , 68 years of age, After Ternelin was administered, patient had the following side effects: glucose urine present, glycosylated haemoglobin increased, proteinuria. During the same period patient was treated with VOLTAREN (Unk) (View Voltaren Review and Voltaren Label ), AMARYL (View Amaryl Review and Amaryl Label ).

6069238-4 | Electrocardiogram Qt Prolonged
on Jan 28, 2009 Male patient from JAPAN , 79 years of age, was diagnosed with musculoskeletal stiffness, conjunctivitis allergic and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: electrocardiogram qt prolonged. Ternelin dosage: Unk. During the same period patient was treated with ZADITEN (Unk) (View Zaditen Review and Zaditen Label ), PLETAL (200 Mg, Qd) (View Pletal Review and Pletal Label ), COVERSYL (4 Mg) (View Coversyl Review and Coversyl Label ), URINORM (50 Mg) (View Urinorm Review and Urinorm Label ), OPALMON (15 Mg) (View Opalmon Review and Opalmon Label ).


5795552-3 | Glucose Urine Present, Glycosylated Haemoglobin Increased, Proteinuria
on Jun 18, 2008 Male patient from JAPAN , 68 years of age, was diagnosed with diabetes mellitus and was treated with Ternelin (View Usage). Patient had the following side effects: glucose urine present, glycosylated haemoglobin increased, proteinuria. Ternelin dosage: Unk. During the same period patient was treated with VOLTAREN (Unk) (View Voltaren Review and Voltaren Label ), AMARYL (View Amaryl Review and Amaryl Label ).

5759849-5 | Glucose Urine Present, Glycosylated Haemoglobin Increased, Proteinuria
Patient was taking Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: glucose urine present, glycosylated haemoglobin increased, proteinuria on May 27, 2008 from JAPAN Additional patient health information: Male patient , 68 years of age, was diagnosed with diabetes mellitus and. Ternelin dosage: Unk. During the same period patient was treated with VOLTAREN (Unk) (View Voltaren Review and Voltaren Label ), AMARYL (View Amaryl Review and Amaryl Label ).

5604035-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Glucose Increased, Blood Lactate Dehydrogenase Increased, Decreased Appetite, Diarrhoea, Hepatic Function Abnormal, Nausea
Adverse event was reported on Jan 18, 2008 by a Female patient taking Ternelin (View Usage) (Dosage: 3 Mg/day) was diagnosed with parkinson's disease (What is parkinson's disease?), blood glucose increased, hypertension and. Location: JAPAN , 76 years of age, weighting 112.4 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood glucose increased, blood lactate dehydrogenase increased, decreased appetite, diarrhoea, hepatic function abnormal, nausea (What is nausea?). During the same period patient was treated with VOGLIBOSE (0.3 Mg, Bid) (View Voglibose Review and Voglibose Label ), YM (9 G, Unk) (View Ym Review and Ym Label ), CHOREITOU (7.5 Mg, Unk) (View Choreitou Review and Choreitou Label ), FORSENID (24 Mg, Unk) (View Forsenid Review and Forsenid Label ), LOXONIN (View Loxonin Review and Loxonin Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ), MAGNESIUM OXIDE (3 G, Unk) (View Magnesium Oxide Review and Magnesium Oxide Label ).

5595569-8 | Alanine Aminotransferase Increased, Anorexia, Aspartate Aminotransferase Increased, Blood Glucose Increased, Blood Lactate Dehydrogenase Increased, Decreased Appetite, Diarrhoea, Hepatic Function Abnormal, Nausea
on Jan 10, 2008 Female patient from JAPAN , 76 years of age, was diagnosed with hypertension and was treated with Ternelin (View Usage). Patient had the following side effects: alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, blood glucose increased, blood lactate dehydrogenase increased, decreased appetite, diarrhoea, hepatic function abnormal, nausea (What is nausea?). Ternelin dosage: . During the same period patient was treated with VOGLIBOSE (0.3 Mg, Bid) (View Voglibose Review and Voglibose Label ), YM (9 G, Unk) (View Ym Review and Ym Label ), CHOREITOU (22.5 Mg, Unk) (View Choreitou Review and Choreitou Label ), FORSENID (View Forsenid Review and Forsenid Label ), LOXONIN (View Loxonin Review and Loxonin Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ), MAGNESIUM OXIDE (3 G, Unk) (View Magnesium Oxide Review and Magnesium Oxide Label ).

5589462-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Decreased Appetite, Diabetes Mellitus, Hepatic Function Abnormal, Hypertension
on Dec 24, 2007 Female patient from JAPAN , 76 years of age, was diagnosed with hypertension and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, diabetes mellitus, hepatic function abnormal, hypertension. Ternelin dosage: (df). During the same period patient was treated with VOGLIBOSE (VOGLIBOSE) ((0.3 Mg Bid Oral)) (View Voglibose (voglibose) Review and Voglibose (voglibose) Label ), DIOVAN (DIOVAN VALSARTAN) ( ((df)) (View Diovan (diovan - Valsartan) ( Review and Diovan (diovan - Valsartan) ( Label ), YM (View Ym Review and Ym Label ), CHOREITOU (View Choreitou Review and Choreitou Label ), FORSENID /00571901/ (View Forsenid /00571901/ Review and Forsenid /00571901/ Label ).

5525414-8 | Dysarthria, Spinal Column Stenosis
Patient was taking Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: dysarthria, spinal column stenosis on Nov 01, 2007 from JAPAN Additional patient health information: Female patient , weighting 132.3 lb, was diagnosed with spinal osteoarthritis and. Ternelin dosage: (3 Mg Qd Oral). During the same period patient was treated with LORCAM (View Lorcam Review and Lorcam Label ), BLOPRESS (View Blopress Review and Blopress Label ), TRICHLORMETHIAZIDE (View Trichlormethiazide Review and Trichlormethiazide Label ), NATRIX (View Natrix Review and Natrix Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), MEILAX (View Meilax Review and Meilax Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

5292645-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Pressure Increased, Condition Aggravated, Gamma-glutamyltransferase Increased, Heart Rate Increased, Liver Disorder, Lymphocyte Stimulation Test Positive
Adverse event was reported on Mar 19, 2007 by a Female patient taking Ternelin (View Usage) (Dosage: 1 Mg Tid Po) was diagnosed with back pain (What is back pain?), hypertension and. Location: JAPAN , 76 years of age, weighting 114.6 lb, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, blood pressure increased, condition aggravated, gamma-glutamyltransferase increased, heart rate increased, liver disorder, lymphocyte stimulation test positive. During the same period patient was treated with CONIEL (Df) (View Coniel Review and Coniel Label ), TENORMIN (25 Mg Qday Po) (View Tenormin Review and Tenormin Label ), OPALMON (View Opalmon Review and Opalmon Label ), LOXONIN (View Loxonin Review and Loxonin Label ), KELNAC (View Kelnac Review and Kelnac Label ), BONALON (View Bonalon Review and Bonalon Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), HALCION (View Halcion Review and Halcion Label ). Patient was hospitalized.

5271849-0 | Blood Potassium Increased, Palpitations, Sinus Arrhythmia
on Mar 02, 2007 Female patient from JAPAN , 50 years of age, was diagnosed with nephrotic syndrome and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: blood potassium increased, palpitations, sinus arrhythmia. Ternelin dosage: Df. During the same period patient was treated with NEORAL (25 Mg Qday Po) (View Neoral Review and Neoral Label ), PREDNISON (View Prednison Review and Prednison Label ), BAKTAR (View Baktar Review and Baktar Label ), MARZULENE S (View Marzulene S Review and Marzulene S Label ), KENTON N (View Kenton N Review and Kenton N Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), VENCOLL (View Vencoll Review and Vencoll Label ), CARTOL (View Cartol Review and Cartol Label ).

5258278-0 | Blood Potassium Increased, Bradycardia, Sinus Arrhythmia
on Feb 16, 2007 Female patient from JAPAN , 50 years of age, was diagnosed with aplasia pure red cell, aplastic anaemia and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: blood potassium increased, bradycardia, sinus arrhythmia. Ternelin dosage: Df Unk Unk. During the same period patient was treated with NEORAL (25 Mg Qday Po) (View Neoral Review and Neoral Label ), PREDNISON (View Prednison Review and Prednison Label ), BAKTAR (View Baktar Review and Baktar Label ), MARZULENE S (View Marzulene S Review and Marzulene S Label ), KENTON N (View Kenton N Review and Kenton N Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), VENCOLL (View Vencoll Review and Vencoll Label ).

5238599-8 | Blood Urea Increased
Patient was taking Ternelin (View Usage). Patient had the following side effects: blood urea increased on Feb 07, 2007 from JAPAN Additional patient health information: Male patient , weighting 160.9 lb, was diagnosed with hypertension and. Ternelin dosage: 1 Mg. During the same period patient was treated with TRIAZOLAM (0.25 Mg) (View Triazolam Review and Triazolam Label ), MUCOSTA (100 Mg) (View Mucosta Review and Mucosta Label ), MOBIC (5 Mg) (View Mobic Review and Mobic Label ), ALDACTONE (50 Mg) (View Aldactone Review and Aldactone Label ), LASIX (20 Mg) (View Lasix Review and Lasix Label ), GASTER (20 Mg) (View Gaster Review and Gaster Label ), MICARDIS (20 Mg) (View Micardis Review and Micardis Label ), AMLODIPINE BESYLATE (5 Mg) (View Amlodipine Besylate Review and Amlodipine Besylate Label ). Patient was hospitalized.

5225896-5 | Blood Pressure Decreased, Body Temperature Decreased, Disease Recurrence, Dysphoria, Gait Disturbance, Heart Rate Decreased, Multiple Sclerosis, Pain In Extremity
Adverse event was reported on Jan 12, 2007 by a Female patient taking Ternelin (View Usage) (Dosage: 3 Mg Qday Po) was diagnosed with multiple sclerosis (What is multiple sclerosis?), pyuria and. Location: JAPAN , 45 years of age, weighting 125.7 lb, After Ternelin was administered, patient had the following side effects: blood pressure decreased, body temperature decreased, disease recurrence, dysphoria, gait disturbance, heart rate decreased, multiple sclerosis (What is multiple sclerosis?), pain in extremity. During the same period patient was treated with CIPROFLOXACIN (400 Mg Qday Po) (View Ciprofloxacin Review and Ciprofloxacin Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

5211818-X | Leukocytoclastic Vasculitis
on Dec 29, 2006 Male patient from JAPAN , 34 years of age, was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: leukocytoclastic vasculitis. Ternelin dosage: Df Unk Po. During the same period patient was treated with LOXOPROFEN SODIUM (View Loxoprofen Sodium Review and Loxoprofen Sodium Label ), ALDIOXA (View Aldioxa Review and Aldioxa Label ).

5186508-2 | Inappropriate Antidiuretic Hormone Secretion
on Nov 27, 2006 Female patient from JAPAN , 80 years of age, was treated with Ternelin (View Usage). Patient had the following side effects: inappropriate antidiuretic hormone secretion. Ternelin dosage: 3 Tab Qday Po. During the same period patient was treated with PANALDINE (View Panaldine Review and Panaldine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), BLOPRESS (View Blopress Review and Blopress Label ), AMARYL (View Amaryl Review and Amaryl Label ), BASEN (View Basen Review and Basen Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), MEDICON (View Medicon Review and Medicon Label ).

5176434-7 | Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased
Patient was taking Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: blood alkaline phosphatase increased, gamma-glutamyltransferase increased on Nov 21, 2006 from JAPAN Additional patient health information: Male patient , 59 years of age, weighting 105.8 lb, was diagnosed with muscle spasms, gastric ulcer, lung neoplasm malignant, angiogram, brain neoplasm and. Ternelin dosage: 1 Mg Tid Po. During the same period patient was treated with PARIET (10 Mg Qday Po) (View Pariet Review and Pariet Label ), MUCODYNE (1500 Mg Qday Po) (View Mucodyne Review and Mucodyne Label ), TS 1 (50 Mg Bid Po) (View Ts 1 Review and Ts 1 Label ), IOPAMIRON (Df Once Iv) (View Iopamiron Review and Iopamiron Label ), NEUROTROPIN (16 Iu Qday Iv) (View Neurotropin Review and Neurotropin Label ), CODEINE PHOSPHATE (60 Mg Qday Po) (View Codeine Phosphate Review and Codeine Phosphate Label ). Patient was hospitalized.

5159261-6 | Blood Pressure Diastolic Decreased, Body Temperature Decreased, Malaise, Vomiting
Adverse event was reported on Nov 02, 2006 by a Female patient taking Ternelin (View Usage) (Dosage: 1 Mg, Bid; Po) was diagnosed with tension headache and. Location: JAPAN , 55 years of age, weighting 116.8 lb, Patient experienced the following unwanted or unexpected effects: blood pressure diastolic decreased, body temperature decreased, malaise, vomiting. During the same period patient was treated with TEGRETOL (View Tegretol Review and Tegretol Label ), VALERIN (View Valerin Review and Valerin Label ), PURSENNID (View Pursennid Review and Pursennid Label ), SEROQUEL (View Seroquel Review and Seroquel Label ), URSO (View Urso Review and Urso Label ), OMEPRAL (View Omepral Review and Omepral Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ).

5154235-3 | Blood Alkaline Phosphatase Increased, Condition Aggravated, Gamma-glutamyltransferase Increased
on Oct 27, 2006 Male patient from JAPAN , 59 years of age, weighting 105.8 lb, was diagnosed with brain neoplasm, gastric ulcer, lung neoplasm malignant and was treated with Ternelin (View Usage). Patient had the following side effects: blood alkaline phosphatase increased, condition aggravated, gamma-glutamyltransferase increased. Ternelin dosage: 1 Mg Tid Po. During the same period patient was treated with PARIET (10 Mg Qday Po) (View Pariet Review and Pariet Label ), MUCODYNE (1500 Mg Qday Po) (View Mucodyne Review and Mucodyne Label ), TS 1 (50 Mg Bid Po) (View Ts 1 Review and Ts 1 Label ), IOPAMIRON (Df Unk Iv) (View Iopamiron Review and Iopamiron Label ), NEUROTROPIN (16 Iu Qday Iv) (View Neurotropin Review and Neurotropin Label ), CODEINE PHOSPHATE (60 Mg Qday Po) (View Codeine Phosphate Review and Codeine Phosphate Label ). Patient was hospitalized.

5062857-3 | Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Liver Disorder
on Jul 06, 2006 Female patient from JAPAN , 74 years of age, weighting 119.0 lb, was diagnosed with rotator cuff syndrome, hyperlipidaemia and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal, liver disorder. Ternelin dosage: Df Po. During the same period patient was treated with LORCAM (Df Po) (View Lorcam Review and Lorcam Label ), SOLON (Df Po) (View Solon Review and Solon Label ), LIPITOR (Df Po) (View Lipitor Review and Lipitor Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), PANTOSIN (View Pantosin Review and Pantosin Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), BONALON (View Bonalon Review and Bonalon Label ). Patient was hospitalized.

4998476-4 | Granulocytopenia, White Blood Cell Count Decreased
Patient was taking Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: granulocytopenia, white blood cell count decreased on Apr 20, 2006 from JAPAN Additional patient health information: Female patient , 15 years of age, was diagnosed with muscle atrophy and. Ternelin dosage: Df Po.

4961634-9 | Headache, Treatment Noncompliance
Adverse event was reported on Mar 13, 2006 by a Male patient taking Ternelin (View Usage) (Dosage: Df Po) was diagnosed with headache (What is headache?) and. Location: JAPAN , 30 years of age, weighting 172.0 lb, Patient had the following side effects: headache (What is headache?), treatment noncompliance. During the same period patient was treated with ERISPAN (Df Po) (View Erispan Review and Erispan Label ), TRYPTANOL (Df Po) (View Tryptanol Review and Tryptanol Label ), DEPAS (Df Prn Po) (View Depas Review and Depas Label ), DICKININ (Df Po) (View Dickinin Review and Dickinin Label ), RIVOTRIL (Df) (View Rivotril Review and Rivotril Label ). Patient was hospitalized.

4883292-4 | Blood Pressure Decreased, Body Temperature Decreased, Difficulty In Walking, Dysphoria, Heart Rate Decreased, Somnolence, Urinary Retention
on Dec 28, 2005 Female patient from JAPAN , 45 years of age, weighting 125.7 lb, was diagnosed with muscle spasticity, pyuria and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: blood pressure decreased, body temperature decreased, difficulty in walking, dysphoria, heart rate decreased, somnolence, urinary retention. Ternelin dosage: 3 Mg Qday Po. During the same period patient was treated with CIPROFLOXACIN (400 Mg Qday Po) (View Ciprofloxacin Review and Ciprofloxacin Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

4851385-3 | Anaphylactic Shock
on Nov 16, 2005 Female patient from JAPAN , 61 years of age, was diagnosed with brachial plexopathy, rhinitis allergic and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock. Ternelin dosage: 3 Mg Once Po. During the same period patient was treated with CLARITIN (10 Mg Once Unk) (View Claritin Review and Claritin Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), EBASTEL (View Ebastel Review and Ebastel Label ), MYONAL (View Myonal Review and Myonal Label ), LOXONIN (View Loxonin Review and Loxonin Label ), SELBEX (View Selbex Review and Selbex Label ).

4819864-2 | Anaphylactic Shock
Patient was taking Ternelin (View Usage). Patient had the following side effects: anaphylactic shock on Oct 17, 2005 from JAPAN Additional patient health information: Female patient , 65 years of age, . Ternelin dosage: Df. During the same period patient was treated with LORATADINE (Df) (View Loratadine Review and Loratadine Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), EBASTEL (View Ebastel Review and Ebastel Label ).

4807163-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Cholesterol Increased, Blood Lactate Dehydrogenase Increased, Erythema, Feeling Hot
Adverse event was reported on Oct 03, 2005 by a Female patient taking Ternelin (View Usage) (Dosage: 3 Mg Qday Po) was diagnosed with deafness, muscle tightness and. Location: JAPAN , 50 years of age, After Ternelin was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood cholesterol increased, blood lactate dehydrogenase increased, erythema, feeling hot. During the same period patient was treated with DORNER (3 Df Qday Po) (View Dorner Review and Dorner Label ), RINDERON (2 G Qday Po) (View Rinderon Review and Rinderon Label ), MELEX (2 G Qday Po) (View Melex Review and Melex Label ), AMOXAN (0.8 G Qday Po) (View Amoxan Review and Amoxan Label ), CLIMAGEN (Df Unk Po) (View Climagen Review and Climagen Label ), EPADEL (3 Df Qday Po) (View Epadel Review and Epadel Label ). Patient was hospitalized.

4775016-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Erythema, Face Oedema, Feeling Hot, Liver Disorder, Pyrexia
on Sep 02, 2005 Female patient from JAPAN , 50 years of age, was diagnosed with deafness, muscle tightness and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, erythema, face oedema, feeling hot, liver disorder, pyrexia. Ternelin dosage: 3 Mg Qday Po. During the same period patient was treated with DORNER (3 Df Qday Po) (View Dorner Review and Dorner Label ), BETAMETHASONE SODIUM PHOSPHATE (2 G Qday Po) (View Betamethasone Sodium Phosphate Review and Betamethasone Sodium Phosphate Label ), MELEX (2 G Qday Po) (View Melex Review and Melex Label ), AMOXAN (0.8 G Qday Po) (View Amoxan Review and Amoxan Label ), CLIMAGEN (Df Po) (View Climagen Review and Climagen Label ). Patient was hospitalized.

4765232-1 | Blood Pressure Decreased, Cardio-respiratory Arrest, Feeling Abnormal, Hypothermia, Loss Of Consciousness, Myocardial Infarction
on Aug 17, 2005 Female patient from JAPAN , 83 years of age, was diagnosed with back pain (What is back pain?) and was treated with Ternelin (View Usage). Patient had the following side effects: blood pressure decreased, cardio-respiratory arrest, feeling abnormal, hypothermia (What is hypothermia?), loss of consciousness, myocardial infarction. Ternelin dosage: 3 Mg Qday Po. During the same period patient was treated with SOLANTAL (150 Mg Qday Po) (View Solantal Review and Solantal Label ), MARZULENE (View Marzulene Review and Marzulene Label ), DIOVAN (View Diovan Review and Diovan Label ), CALSLOT (View Calslot Review and Calslot Label ). Patient was hospitalized.

4736412-6 | Chest Pain, Hypoaesthesia, Peripheral Coldness
Patient was taking Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: chest pain (What is chest pain?), hypoaesthesia, peripheral coldness on Jul 15, 2005 from JAPAN Additional patient health information: Male patient , 56 years of age, . Ternelin dosage: Df.

4718975-X | Body Temperature Decreased, Myocardial Infarction
Adverse event was reported on Jun 30, 2005 by a Female patient taking Ternelin (View Usage) (Dosage: 1 Mg Qday; Po) was diagnosed with back pain (What is back pain?) and. Location: JAPAN , 83 years of age, Patient experienced the following unwanted or unexpected effects: body temperature decreased, myocardial infarction. During the same period patient was treated with SOLANTAL (50 Mg Qday; Po) (View Solantal Review and Solantal Label ), MARZULENE (View Marzulene Review and Marzulene Label ). Patient was hospitalized.

4710995-4 | Erythema, Hypotension, Rash, Vomiting
on Jun 23, 2005 Female patient from JAPAN , 62 years of age, was diagnosed with arthralgia and was treated with Ternelin (View Usage). Patient had the following side effects: erythema, hypotension, rash (What is rash?), vomiting. Ternelin dosage: 2 Mg Qday Po. During the same period patient was treated with VOLTAREN (75 Mg Qday Po) (View Voltaren Review and Voltaren Label ), MUCOSTA (2 Df Qday) (View Mucosta Review and Mucosta Label ). Patient was hospitalized.

4693790-4 | Exanthem, Hypotension, Vomiting
on May 31, 2005 Female patient from , 62 years of age, was diagnosed with arthralgia and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: exanthem, hypotension, vomiting. Ternelin dosage: 2 Mg Qday Po. During the same period patient was treated with VOLTAREN (75 Mg Qday Po) (View Voltaren Review and Voltaren Label ), MUCOSTA (2 Df Qday) (View Mucosta Review and Mucosta Label ). Patient was hospitalized.

4643080-0 | Chest Pain, Peripheral Coldness
Patient was taking Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), peripheral coldness on Apr 05, 2005 from Additional patient health information: Male patient , 53 years of age, . Ternelin dosage: Df.

4633339-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Gamma-glutamyltransferase Abnormal, Liver Disorder, Lymphocyte Stimulation Test Positive
Adverse event was reported on Mar 24, 2005 by a Female patient taking Ternelin (View Usage) (Dosage: 3 Mg Qday Po) was diagnosed with intervertebral disc protrusion and. Location: , 27 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), gamma-glutamyltransferase abnormal, liver disorder, lymphocyte stimulation test positive. During the same period patient was treated with VOLTAREN (75 Mg Qday Po) (View Voltaren Review and Voltaren Label ), MUCOSTA (300 Mg Qday Po) (View Mucosta Review and Mucosta Label ), MECOBALAMIN (View Mecobalamin Review and Mecobalamin Label ). Patient was hospitalized.

4633338-3 | Lymphocyte Stimulation Test Positive, Pigmentation Disorder, Rash, Toxic Skin Eruption, Urticaria
on Mar 24, 2005 Male patient from , 27 years of age, was diagnosed with back pain (What is back pain?), gastritis, nasopharyngitis and was treated with Ternelin (View Usage). After Ternelin was administered, patient had the following side effects: lymphocyte stimulation test positive, pigmentation disorder, rash (What is rash?), toxic skin eruption, urticaria. Ternelin dosage: Po. During the same period patient was treated with PEON (View Peon Review and Peon Label ), MARZULENE S (View Marzulene S Review and Marzulene S Label ), DAN RICH (View Dan Rich Review and Dan Rich Label ), OVER THE COUNTER ANTITUSSIVES (NOS) (View Over-the - Counter Antitussives (nos) Review and Over-the - Counter Antitussives (nos) Label ).

4627700-2 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Calcium Increased, Blood Lactate Dehydrogenase Increased, Blood Potassium Increased, Blood Pressure Systolic Increased, Blood Sodium Decreased, Body Temperature Decreased
on Mar 18, 2005 Male patient from , 40 years of age, was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, blood calcium increased, blood lactate dehydrogenase increased, blood potassium increased, blood pressure systolic increased, blood sodium decreased, body temperature decreased. Ternelin dosage: 20 Mg Once Po. During the same period patient was treated with ROHYPNOL (46 Mg Once Po) (View Rohypnol Review and Rohypnol Label ), HALCION (2.5 Mg Once Po) (View Halcion Review and Halcion Label ), LORAZEPAM (20 Mg Once Po) (View Lorazepam Review and Lorazepam Label ), SLOWHEIM (75 Mg Once Po) (View Slowheim Review and Slowheim Label ), VITAMIN A (600 Mg Once Po) (View Vitamin A Review and Vitamin A Label ). Patient was hospitalized.

4603071-2 | Lymphocyte Stimulation Test Positive, Toxic Skin Eruption, Urticaria
Patient was taking Ternelin (View Usage). Patient had the following side effects: lymphocyte stimulation test positive, toxic skin eruption, urticaria on Feb 18, 2005 from Additional patient health information: Male patient , 27 years of age, was diagnosed with back pain (What is back pain?), gastritis and. Ternelin dosage: Po. During the same period patient was treated with PEON (View Peon Review and Peon Label ), MARZULENE S (View Marzulene S Review and Marzulene S Label ).

4576254-8 | Convulsion, Disease Recurrence, Dyspnoea, Epilepsy, Hyperventilation, Myoclonus, Oxygen Saturation Decreased, Serotonin Syndrome
Adverse event was reported on Jan 20, 2005 by a Female patient taking Ternelin (View Usage) (Dosage: Df Qday Po) was diagnosed with hypertonia, depression (What is depression?) and. Location: , 27 years of age, After Ternelin was administered, patient had the following side effects: convulsion, disease recurrence, dyspnoea, epilepsy (What is epilepsy?), hyperventilation, myoclonus, oxygen saturation decreased, serotonin syndrome. During the same period patient was treated with PAXIL (35 Mg Qday Po) (View Paxil Review and Paxil Label ), LEXOTAN (Df) (View Lexotan Review and Lexotan Label ).

4563646-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Liver Disorder, Lymphocyte Stimulation Test Positive
on Jan 06, 2005 Female patient from , 27 years of age, was diagnosed with intervertebral disc protrusion and was treated with Ternelin (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), liver disorder, lymphocyte stimulation test positive. Ternelin dosage: 3 Mg Qday Po. During the same period patient was treated with VOLTAREN (75 Mg Qday Po) (View Voltaren Review and Voltaren Label ), MUCOSTA (300 Mg Qday Po) (View Mucosta Review and Mucosta Label ), MECOBALAMIN (View Mecobalamin Review and Mecobalamin Label ). Patient was hospitalized.

4551309-2 | Respiratory Disorder, Serotonin Syndrome, Tremor
on Dec 23, 2004 Female patient from , 27 years of age, was diagnosed with hypertonia, depression (What is depression?) and was treated with Ternelin (View Usage). Patient had the following side effects: respiratory disorder, serotonin syndrome, tremor. Ternelin dosage: Df Qday Po. During the same period patient was treated with PAXIL (Df Po) (View Paxil Review and Paxil Label ).


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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 Ternelin 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 Ternelin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ternelin 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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Ternelin 2mg twice a day Side Effect Report#5799 very low blood pressure, low pulse rate fatigue.severe headache,couldn\'t do daily routine work while taking medicine ...

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... Unk) (View Loxonin Review and Loxonin Label ), BALANCE (Unk) (View Balance Review and Balance Label ), TERNELIN (Unk) (View Ternelin Review and Ternelin Label ), LACTOSE (Unk ...

During the same period patient was treated with LOXONIN (60 Mg Tid Po) (View Loxonin Review and Loxonin Label ), TERNELIN (View Ternelin Review and Ternelin Label ), APLACE ...

... patient was treated with TERNELIN (View Ternelin Review and Ternelin Label ), FLOMOX ... was reported on Jul 07, 2005 by a Male patient taking Cefazolin (Dosage: 100mg ...

... Flomox Label ), COUGHNOL (View Coughnol Review and Coughnol Label ), MAGMITT (View Magmitt Review and Magmitt Label ), TERNELIN (View Ternelin Review and Ternelin Label ), ...

... dantrolene Sodium) (nr) Label ), TERNELIN (TIZANIDINE HYDROCHLORIDE) (NR) (1 Mg Tid (nr, Tid) Po) (View Ternelin (tizanidine Hydrochloride) (nr) Review and Ternelin ...

During the same period patient was treated with TERNELIN (View Ternelin Review and Ternelin Label ), FLOMOX (View Flomox Review and Flomox Label ), CRAVIT (View Cravit Review ...

... Flomox Label ), COUGHNOL (View Coughnol Review and Coughnol Label ), MAGMITT (View Magmitt Review and Magmitt Label ), TERNELIN (View Ternelin Review and Ternelin Label ), ...

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Ternelin Reactions
Alanine Aminotransferase Increased
Altered State Of Consciousness
Anaphylactic Shock
Aspartate Aminotransferase Increased
Back PainWhat is Back pain?
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Glucose Increased
Blood Lactate Dehydrogenase Increased
Blood Potassium Increased
Blood Pressure Decreased
Blood Pressure Increased
Body Temperature Decreased
Chest PainWhat is Chest pain?
Condition Aggravated
Decreased Appetite
Diarrhoea
Disease Recurrence
Dysphoria
Erythema
Gamma-glutamyltransferase Increased
Glucose Urine Present
Glycosylated Haemoglobin Increased
Hepatic Function Abnormal
Hypotension
Liver Disorder
Lymphocyte Stimulation Test Positive
Proteinuria
Somnolence
Vomiting
Ternelin 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 Ternelin 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!