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Summary

FDA Adverse Reports: 56. View All

Amlodin FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 24

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

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6819452-2 | Convulsion
on Jun 29, 2010 Female patient from JAPAN , 40 years of age, was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion. Amlodin dosage: .

6812986-6 | Blood Creatine Phosphokinase Increased
Patient was taking Amlodin (View Usage). Patient had the following side effects: blood creatine phosphokinase increased on Jun 23, 2010 from JAPAN Additional patient health information: Male patient , 63 years of age, . Amlodin dosage: . Patient was hospitalized.

6789995-9 | Intentional Overdose, Renal Failure Acute, Rhabdomyolysis
Adverse event was reported on Jun 16, 2010 by a Female patient taking Amlodin (View Usage) (Dosage: Unk) . Location: JAPAN , 36 years of age, After Amlodin was administered, patient had the following side effects: intentional overdose, renal failure acute, rhabdomyolysis. During the same period patient was treated with MYSLEE (Unk) (View Myslee Review and Myslee Label ).

6763881-2 | Chromaturia
on May 31, 2010 Male patient from JAPAN , 64 years of age, was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: chromaturia. Amlodin dosage: .


6734944-2 | Cardio-respiratory Arrest, Hyperglycaemia, Overdose
on May 12, 2010 Female patient from JAPAN , 68 years of age, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: cardio-respiratory arrest, hyperglycaemia, overdose. Amlodin dosage: . During the same period patient was treated with HERBESSER R (View Herbesser R Review and Herbesser R Label ), VALSARTAN (Unk) (View Valsartan Review and Valsartan Label ).

6718210-7 | Parkinsonism
Patient was taking Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: parkinsonism on Apr 30, 2010 from JAPAN Additional patient health information: Female patient , 61 years of age, . Amlodin dosage: 5 Mg, Daily.

6706749-X | Cardio-respiratory Arrest, Hyperglycaemia, Overdose
Adverse event was reported on Apr 23, 2010 by a Female patient taking Amlodin (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 68 years of age, Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, hyperglycaemia, overdose. During the same period patient was treated with HERBESSER R (View Herbesser R Review and Herbesser R Label ), VALSARTAN (Unk) (View Valsartan Review and Valsartan Label ).

6698621-9 | Cardio-respiratory Arrest, Hyperglycaemia, Overdose
on Apr 15, 2010 Female patient from JAPAN , 68 years of age, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: cardio-respiratory arrest, hyperglycaemia, overdose. Amlodin dosage: . During the same period patient was treated with HERBESSER R (View Herbesser R Review and Herbesser R Label ), DIOVANE (Unk) (View Diovane Review and Diovane Label ).

6470370-1 | Atrial Fibrillation, Bradycardia, Hyperkalaemia, Renal Failure Acute, Shock
on Jun 02, 2009 Male patient from JAPAN , 82 years of age, was diagnosed with hypertension, thyroid cancer (What is thyroid cancer?), goitre and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), bradycardia, hyperkalaemia, renal failure acute, shock. Amlodin dosage: 5 Mg, 1x/day. During the same period patient was treated with ATENOLOL (50 Mg, 1x/day) (View Atenolol Review and Atenolol Label ), BLOPRESS (12 Mg, 1x/day) (View Blopress Review and Blopress Label ), ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), CLARITH (200 Mg, 1x/day) (View Clarith Review and Clarith Label ), LEVOTHYROXINE SODIUM (50 Ug, 1x/day) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

6076053-4 |
Patient was taking Amlodin (View Usage). on Jan 30, 2009 from JAPAN Additional patient health information: Male patient , weighting 149.9 lb, was diagnosed with hypertension, lacunar infarction and. Amlodin dosage: 5 Mg. During the same period patient was treated with CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ).

5967582-X | Blood Pressure Inadequately Controlled, Hepatic Failure
Adverse event was reported on Nov 07, 2008 by a Female patient taking Amlodin (View Usage) (Dosage: ) was diagnosed with disseminated tuberculosis, hypertension and. Location: JAPAN , 60 years of age, Patient had the following side effects: blood pressure inadequately controlled, hepatic failure. During the same period patient was treated with SELECTOL (View Selectol Review and Selectol Label ), PYRAZINAMIDE (View Pyrazinamide Review and Pyrazinamide Label ), RIFADIN (View Rifadin Review and Rifadin Label ), ISCOTIN (View Iscotin Review and Iscotin Label ), ACECOL (View Acecol Review and Acecol Label ), ARTIST (View Artist Review and Artist Label ).

5955776-9 | Leukocytoclastic Vasculitis, Tubulointerstitial Nephritis
on Nov 06, 2008 Female patient from JAPAN , weighting 125.0 lb, was diagnosed with hypertension, cholelithiasis, cerebral infarction, rhinitis allergic and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: leukocytoclastic vasculitis, tubulointerstitial nephritis. Amlodin dosage: Daily Dose:5mg. During the same period patient was treated with ENALAPRIL MALEATE (Daily Dose:5mg) (View Enalapril Maleate Review and Enalapril Maleate Label ), URSO 250 (Daily Dose:200mg-freq:frequency: Daily) (View Urso 250 Review and Urso 250 Label ), MUCODYNE (Daily Dose:1500mg-freq:frequency: Daily) (View Mucodyne Review and Mucodyne Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), UNIPHYL (Daily Dose:200mg) (View Uniphyl Review and Uniphyl Label ), CLARITIN (Daily Dose:10mg-freq:frequency: Daily) (View Claritin Review and Claritin Label ), MONTELUKAST SODIUM (Daily Dose:10mg-freq:frequency: Daily) (View Montelukast Sodium Review and Montelukast Sodium Label ), INTAL (View Intal Review and Intal Label ). Patient was hospitalized.

5945333-2 | Interstitial Lung Disease
on Oct 30, 2008 Male patient from JAPAN , 77 years of age, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Amlodin dosage: Daily Dose:5mg. Patient was hospitalized.

5939047-2 | Adverse Reaction
Patient was taking Amlodin (View Usage). Patient had the following side effects: adverse reaction on Oct 23, 2008 from JAPAN Additional patient health information: Male patient , weighting 149.9 lb, was diagnosed with hypertension, lacunar infarction and. Amlodin dosage: 5 Mg. During the same period patient was treated with CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ).

5938011-7 | Atrioventricular Block
Adverse event was reported on Oct 22, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: ) . Location: JAPAN , 73 years of age, After Amlodin was administered, patient had the following side effects: atrioventricular block. During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), HARNAL (View Harnal Review and Harnal Label ), ALOSITOL (View Alositol Review and Alositol Label ), LASIX (View Lasix Review and Lasix Label ), NU LOTAN (View Nu Lotan Review and Nu Lotan Label ), BASEN (View Basen Review and Basen Label ), SERMION (View Sermion Review and Sermion Label ), KETAS (View Ketas Review and Ketas Label ). Patient was hospitalized.

5928367-3 | Blood Creatinine Increased
on Oct 07, 2008 Male patient from JAPAN , 60 years of age, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased. Amlodin dosage: . During the same period patient was treated with MICARDIS (Daily Dose:40mg) (View Micardis Review and Micardis Label ).

5927239-8 | Overdose
on Oct 06, 2008 Female patient from JAPAN , 75 years of age, was treated with Amlodin (View Usage). Patient had the following side effects: overdose. Amlodin dosage: . Patient was hospitalized.

5918079-4 | Atrioventricular Block
Patient was taking Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: atrioventricular block on Oct 03, 2008 from JAPAN Additional patient health information: Male patient , 73 years of age, . Amlodin dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), HARNAL (View Harnal Review and Harnal Label ), ALOSITOL (View Alositol Review and Alositol Label ), LASIX (View Lasix Review and Lasix Label ), NU LOTAN (View Nu Lotan Review and Nu Lotan Label ), BASEN (View Basen Review and Basen Label ), SERMION (View Sermion Review and Sermion Label ), KETAS (View Ketas Review and Ketas Label ). Patient was hospitalized.

5743304-2 | Blood Creatinine Increased, Blood Urea Increased, Hypotension
Adverse event was reported on May 09, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: Daily Dose:10mg-freq:qd) was diagnosed with hypertension and. Location: JAPAN , 64 years of age, weighting 114.6 lb, Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood urea increased, hypotension. During the same period patient was treated with KLACID (Daily Dose:400mg) (View Klacid Review and Klacid Label ), ARTIST (View Artist Review and Artist Label ), ITOROL (View Itorol Review and Itorol Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GLYSENNID (View Glysennid Review and Glysennid Label ), LIPITOR (View Lipitor Review and Lipitor Label ), CHOLEBRINE (View Cholebrine Review and Cholebrine Label ). Patient was hospitalized.

5743279-6 | Anaemia, Haemoglobin Decreased
on May 07, 2008 Female patient from JAPAN , 71 years of age, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: anaemia, haemoglobin decreased. Amlodin dosage: Daily Dose:5mg. During the same period patient was treated with RIDAURA (Daily Dose:6mg) (View Ridaura Review and Ridaura Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), VALSARTAN (Daily Dose:160mg) (View Valsartan Review and Valsartan Label ), AMARYL (Daily Dose:1mg) (View Amaryl Review and Amaryl Label ), PREDONINE (Daily Dose:6mg) (View Predonine Review and Predonine Label ), PARIET (Daily Dose:10mg) (View Pariet Review and Pariet Label ), EVISTA (Daily Dose:60mg) (View Evista Review and Evista Label ). Patient was hospitalized.

5735599-6 | Toxic Epidermal Necrolysis
on Apr 28, 2008 Female patient from JAPAN , weighting 118.6 lb, was diagnosed with hypertension, constipation (What is constipation?) and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: toxic epidermal necrolysis. Amlodin dosage: . During the same period patient was treated with LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ), ALOSENN (View Alosenn Review and Alosenn Label ), DIOVANE (View Diovane Review and Diovane Label ). Patient was hospitalized.

5720348-8 | Bradycardia, Nausea, Renal Disorder
Patient was taking Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, nausea (What is nausea?), renal disorder on Apr 18, 2008 from JAPAN Additional patient health information: Female patient , weighting 91.05 lb, was diagnosed with hypertension and. Amlodin dosage: Daily Dose:5mg. During the same period patient was treated with DIGOXIN (Daily Dose:.125mg) (View Digoxin Review and Digoxin Label ), ASPARA CA (Daily Dose:400mg) (View Aspara-ca Review and Aspara-ca Label ), BEZATOL SLOW RELEASE (Daily Dose:200mg) (View Bezatol - Slow Release Review and Bezatol - Slow Release Label ), RIVOTRIL (Daily Dose:.5mg) (View Rivotril Review and Rivotril Label ), CYANOCOBALAMIN (Daily Dose:1500mcg) (View Cyanocobalamin Review and Cyanocobalamin Label ), TERNELIN (Daily Dose:3mg) (View Ternelin Review and Ternelin Label ), NATEGLINIDE (Daily Dose:270mg) (View Nateglinide Review and Nateglinide Label ), FAMOTIDINE (Daily Dose:20mg) (View Famotidine Review and Famotidine Label ). Patient was hospitalized.

5717095-5 | Blood Creatinine Increased, Blood Urea Increased, Hypotension
Adverse event was reported on Apr 15, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: Daily Dose:10mg-freq:qd) was diagnosed with hypertension and. Location: JAPAN , 64 years of age, weighting 114.6 lb, Patient had the following side effects: blood creatinine increased, blood urea increased, hypotension. During the same period patient was treated with KLACID (Daily Dose:400mg) (View Klacid Review and Klacid Label ), ARTIST (View Artist Review and Artist Label ), ITOROL (View Itorol Review and Itorol Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GLYSENNID (View Glysennid Review and Glysennid Label ), LIPITOR (View Lipitor Review and Lipitor Label ), CHOLEBRINE (View Cholebrine Review and Cholebrine Label ). Patient was hospitalized.

5707621-4 | Bradycardia, Renal Disorder, Vomiting
on Apr 04, 2008 Female patient from JAPAN , weighting 91.05 lb, was diagnosed with hypertension and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: bradycardia, renal disorder, vomiting. Amlodin dosage: . During the same period patient was treated with DIGOXIN (Daily Dose:.125mg) (View Digoxin Review and Digoxin Label ), ASPARA CA (Daily Dose:400mg) (View Aspara-ca Review and Aspara-ca Label ), BEZATOL SLOW RELEASE (Daily Dose:200mg) (View Bezatol - Slow Release Review and Bezatol - Slow Release Label ), RIVOTRIL (Daily Dose:.5mg) (View Rivotril Review and Rivotril Label ), CYANOCOBALAMIN (Text:3 Dosage Form) (View Cyanocobalamin Review and Cyanocobalamin Label ), TERNELIN (Daily Dose:3mg) (View Ternelin Review and Ternelin Label ), NATEGLINIDE (Daily Dose:270mg) (View Nateglinide Review and Nateglinide Label ), FAMOTIDINE (Daily Dose:20mg) (View Famotidine Review and Famotidine Label ). Patient was hospitalized.

5706186-0 | Eosinophilia, Eosinophilic Pneumonia, Thrombocytopenia
on Apr 03, 2008 Male patient from JAPAN , 53 years of age, weighting 129.0 lb, was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: eosinophilia, eosinophilic pneumonia, thrombocytopenia. Amlodin dosage: Daily Dose:10mg. During the same period patient was treated with FAMOTIDINE (Daily Dose:10mg) (View Famotidine Review and Famotidine Label ), HYDROCORTISONE (Daily Dose:10mg) (View Hydrocortisone Review and Hydrocortisone Label ), METOPROLOL TARTRATE (Daily Dose:20mg) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), NIFEDIPINE (Daily Dose:40mg) (View Nifedipine Review and Nifedipine Label ), OLMESARTAN MEDOXOMIL (Daily Dose:40mg) (View Olmesartan Medoxomil Review and Olmesartan Medoxomil Label ), BERAPROST SODIUM (Daily Dose:120mcg) (View Beraprost Sodium Review and Beraprost Sodium Label ), MECOBALAMIN (Daily Dose:1500mcg) (View Mecobalamin Review and Mecobalamin Label ), SEVELAMER HYDROCHLORIDE (Daily Dose:2.25gram) (View Sevelamer Hydrochloride Review and Sevelamer Hydrochloride Label ). Patient was hospitalized.

5703633-5 | Toxic Epidermal Necrolysis
Patient was taking Amlodin (View Usage). Patient had the following side effects: toxic epidermal necrolysis on Apr 03, 2008 from JAPAN Additional patient health information: Female patient , weighting 118.6 lb, was diagnosed with hypertension, constipation (What is constipation?) and. Amlodin dosage: . During the same period patient was treated with LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ), ALOSENN (View Alosenn Review and Alosenn Label ), DIOVAN (View Diovan Review and Diovan Label ). Patient was hospitalized.

5703065-X | Parkinson's Disease
Adverse event was reported on Apr 07, 2008 by a Female patient taking Amlodin (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: TUNISIA , 68 years of age, After Amlodin was administered, patient had the following side effects: parkinson's disease (What is parkinson's disease?). During the same period patient was treated with ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

5698192-X | Blood Creatinine Increased, Blood Urea Increased, Dehydration, Hypotension, Large Intestine Carcinoma, Malnutrition, Pneumonia, Recurrent Cancer
on Mar 26, 2008 Male patient from JAPAN , 65 years of age, weighting 114.6 lb, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood urea increased, dehydration, hypotension, large intestine carcinoma, malnutrition, pneumonia (What is pneumonia?), recurrent cancer. Amlodin dosage: Daily Dose:10mg-freq:qd. During the same period patient was treated with KLACID (Daily Dose:400mg) (View Klacid Review and Klacid Label ).

5697419-8 | Peritoneal Dialysis, Renal Failure Chronic
on Mar 27, 2008 Male patient from JAPAN , 60 years of age, weighting 119.0 lb, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: peritoneal dialysis, renal failure chronic. Amlodin dosage: 5 Mg, Unk. During the same period patient was treated with CARDENALIN (1 Df, Unk) (View Cardenalin Review and Cardenalin Label ), DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ).

5694956-7 | Amniotic Cavity Disorder, Oligohydramnios, Premature Labour, Premature Rupture Of Membranes, Renal Disorder, Renal Hypertrophy, Renal Impairment Neonatal
Patient was taking Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: amniotic cavity disorder, oligohydramnios, premature labour, premature rupture of membranes, renal disorder, renal hypertrophy, renal impairment neonatal on Mar 21, 2008 from JAPAN Additional patient health information: Female patient , 34 years of age, weighting 114.6 lb, was diagnosed with hypertension and. Amlodin dosage: 5 Mg, Unk. During the same period patient was treated with DIOVAN (80 Mg/day) (View Diovan Review and Diovan Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ). Patient was hospitalized.

5693248-X | Alanine Aminotransferase Increased, Anorexia, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Potassium Decreased, Blood Urea Increased, Haematocrit Decreased
Adverse event was reported on Mar 27, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: 5 Mg) was diagnosed with hyperlipidaemia and. Location: JAPAN , 65 years of age, weighting 154.3 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood potassium decreased, blood urea increased, haematocrit decreased. During the same period patient was treated with ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), NORVASC (5 Mg, Unk) (View Norvasc Review and Norvasc Label ), BLOPRESS (4 Mg, Unk) (View Blopress Review and Blopress Label ), CARDENALIN (2 Mg, Unk) (View Cardenalin Review and Cardenalin Label ), LOCHOL (20 Mg/ Day) (View Lochol Review and Lochol Label ), PLASMA (View Plasma Review and Plasma Label ). Patient was hospitalized.

5689563-6 | Bradycardia, Renal Disorder, Vomiting
on Mar 19, 2008 Female patient from JAPAN , weighting 91.05 lb, was diagnosed with hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: bradycardia, renal disorder, vomiting. Amlodin dosage: . During the same period patient was treated with DIGOXIN (Daily Dose:.125mg) (View Digoxin Review and Digoxin Label ), ASPARA CA (Daily Dose:400mg) (View Aspara-ca Review and Aspara-ca Label ), BEZATOL SLOW RELEASE (Daily Dose:200mg) (View Bezatol - Slow Release Review and Bezatol - Slow Release Label ), RIVOTRIL (Daily Dose:.5mg) (View Rivotril Review and Rivotril Label ), CYANOCOBALAMIN (Text:3 Dosage Form) (View Cyanocobalamin Review and Cyanocobalamin Label ), TERNELIN (Daily Dose:3mg) (View Ternelin Review and Ternelin Label ), NATEGLINIDE (Daily Dose:270mg) (View Nateglinide Review and Nateglinide Label ), FAMOTIDINE (Daily Dose:20mg) (View Famotidine Review and Famotidine Label ). Patient was hospitalized.

5689464-3 | Blood Creatinine Increased, Blood Urea Increased
on Mar 21, 2008 Male patient from JAPAN , 65 years of age, was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: blood creatinine increased, blood urea increased. Amlodin dosage: Daily Dose:10mg-freq:qd. During the same period patient was treated with KLARICID (View Klaricid Review and Klaricid Label ).

5682231-6 | Amniotic Cavity Disorder, Oligohydramnios, Polyhydramnios, Premature Labour, Premature Rupture Of Membranes, Renal Disorder, Renal Hypertrophy, Renal Impairment Neonatal
Patient was taking Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: amniotic cavity disorder, oligohydramnios, polyhydramnios, premature labour, premature rupture of membranes, renal disorder, renal hypertrophy, renal impairment neonatal on Mar 21, 2008 from JAPAN Additional patient health information: Female patient , 34 years of age, weighting 114.6 lb, was diagnosed with hypertension and. Amlodin dosage: 5 Mg, Unk. During the same period patient was treated with DIOVAN (80 Mg/day) (View Diovan Review and Diovan Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ). Patient was hospitalized.

5675088-0 | Blood Creatinine Increased, Blood Urea Increased
Adverse event was reported on Mar 10, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: Daily Dose:10mg-freq:qd) . Location: JAPAN , 65 years of age, Patient had the following side effects: blood creatinine increased, blood urea increased.

5670525-X | Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Creatinine Increased, Blood Potassium Decreased, Blood Sodium Decreased, Blood Urea Increased, Haematocrit Decreased, Haemoglobin Decreased, Liver Function Test Abnormal
on Mar 11, 2008 Male patient from JAPAN , 65 years of age, weighting 154.3 lb, was diagnosed with hyperlipidaemia and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, haematocrit decreased, haemoglobin decreased, liver function test abnormal. Amlodin dosage: 5 Mg. During the same period patient was treated with ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), NORVASC (5 Mg, Unk) (View Norvasc Review and Norvasc Label ), BLOPRESS (4 Mg, Unk) (View Blopress Review and Blopress Label ), CARDENALIN (2 Mg, Unk) (View Cardenalin Review and Cardenalin Label ), FLUVASTATIN (20 Mg/ Day) (View Fluvastatin Review and Fluvastatin Label ). Patient was hospitalized.

5669929-0 | Eosinophil Count Increased, Granulocyte Count Decreased, Lymphadenitis, Lymphocyte Stimulation Test Positive, Neutrophil Count Decreased, Skin Exfoliation
on Mar 05, 2008 Female patient from JAPAN , 84 years of age, was diagnosed with hypertension, gastritis, hyperuricaemia and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: eosinophil count increased, granulocyte count decreased, lymphadenitis, lymphocyte stimulation test positive, neutrophil count decreased, skin exfoliation. Amlodin dosage: . During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), ALLORINE (View Allorine Review and Allorine Label ), CLARITIN (View Claritin Review and Claritin Label ), CARBON TABLETS (View Carbon Tablets Review and Carbon Tablets Label ), LABETALOL HCL (View Labetalol Hcl Review and Labetalol Hcl Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5665017-8 | Interstitial Lung Disease, Pancytopenia, Pneumonia
Patient was taking Amlodin (View Usage). Patient had the following side effects: interstitial lung disease, pancytopenia, pneumonia (What is pneumonia?) on Mar 05, 2008 from JAPAN Additional patient health information: Female patient , 66 years of age, . Amlodin dosage: Daily Dose:5mg.

5661622-3 | Peritoneal Dialysis, Renal Failure Chronic
Adverse event was reported on Mar 03, 2008 by a Male patient taking Amlodin (View Usage) (Dosage: 5 Mg, Unk) was diagnosed with hypertension and. Location: JAPAN , 60 years of age, weighting 119.0 lb, After Amlodin was administered, patient had the following side effects: peritoneal dialysis, renal failure chronic. During the same period patient was treated with CARDENALIN (1 Df, Unk) (View Cardenalin Review and Cardenalin Label ), DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ).

5661561-8 | Thrombotic Thrombocytopenic Purpura
on Mar 06, 2008 Male patient from JAPAN , 65 years of age, was diagnosed with hyperlipidaemia and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: thrombotic thrombocytopenic purpura. Amlodin dosage: 5 Mg. During the same period patient was treated with FLUVASTATIN (20 Mg/ Day) (View Fluvastatin Review and Fluvastatin Label ).

5649654-2 | Dizziness, Femur Fracture
on Feb 21, 2008 Female patient from JAPAN , 62 years of age, was diagnosed with essential hypertension and was treated with Amlodin (View Usage). Patient had the following side effects: dizziness (What is dizziness?), femur fracture. Amlodin dosage: . During the same period patient was treated with OLMESARTAN MEDOXOMIL (View Olmesartan Medoxomil Review and Olmesartan Medoxomil Label ), TENORMIN (View Tenormin Review and Tenormin Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), DEPAS (View Depas Review and Depas Label ). Patient was hospitalized.

5628545-7 | Femur Fracture
Patient was taking Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: femur fracture on Feb 05, 2008 from JAPAN Additional patient health information: Female patient , 62 years of age, was diagnosed with essential hypertension and. Amlodin dosage: . During the same period patient was treated with OLMETEC (View Olmetec Review and Olmetec Label ), TENORMIN (View Tenormin Review and Tenormin Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), DEPAS (View Depas Review and Depas Label ). Patient was hospitalized.

5564124-8 | Balance Disorder, Chest Pain, Pain In Extremity, Tremor, Visual Acuity Reduced
Adverse event was reported on Dec 05, 2007 by a Female patient taking Amlodin (View Usage) (Dosage: Text:1 Df-freq:daily) was diagnosed with hypertension, gastrooesophageal reflux disease, anxiety (What is anxiety?) and. Location: UNITED KINGDOM , weighting 198.4 lb, Patient experienced the following unwanted or unexpected effects: balance disorder, chest pain (What is chest pain?), pain in extremity, tremor, visual acuity reduced. During the same period patient was treated with OMEPRAZOLE (Daily Dose:20mg-freq:daily) (View Omeprazole Review and Omeprazole Label ), PROTHIADEN (Daily Dose:25mg-freq:daily) (View Prothiaden Review and Prothiaden Label ).

5384746-7 | Discomfort, Facial Spasm, Pharyngolaryngeal Pain, Rhabdomyolysis
on Jun 29, 2007 Female patient from JAPAN , weighting 147.7 lb, was diagnosed with hypertension, hyperlipidaemia and was treated with Amlodin (View Usage). Patient had the following side effects: discomfort, facial spasm, pharyngolaryngeal pain, rhabdomyolysis. Amlodin dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), CONIEL (View Coniel Review and Coniel Label ), BLOPRESS (View Blopress Review and Blopress Label ).

5324958-1 | Dizziness, Headache, Nausea, Obsessive-compulsive Disorder
on May 08, 2007 Male patient from JAPAN , 60 years of age, was diagnosed with nail tinea and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: dizziness (What is dizziness?), headache (What is headache?), nausea (What is nausea?), obsessive-compulsive disorder (What is obsessive-compulsive disorder?). Amlodin dosage: 5 Mg/day. During the same period patient was treated with LAMISIL (125 Mg/day) (View Lamisil Review and Lamisil Label ).

5324905-2 | Dizziness, Headache, Nausea, Obsessive-compulsive Disorder
Patient was taking Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), headache (What is headache?), nausea (What is nausea?), obsessive-compulsive disorder (What is obsessive-compulsive disorder?) on May 08, 2007 from JAPAN Additional patient health information: Male patient , 60 years of age, was diagnosed with nail tinea and. Amlodin dosage: 5 Mg/day. During the same period patient was treated with LAMISIL (125 Mg/day) (View Lamisil Review and Lamisil Label ).

5296870-8 | Atrioventricular Block, Bradycardia, Dyspnoea, Oedema
Adverse event was reported on Apr 06, 2007 by a Female patient taking Amlodin (View Usage) (Dosage: Daily Dose:2.5mg-freq:daily) was diagnosed with hypertension, dementia alzheimer's type and. Location: JAPAN , 87 years of age, Patient had the following side effects: atrioventricular block, bradycardia, dyspnoea, oedema. During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ).

5267779-0 | Hepatitis Fulminant
on Mar 05, 2007 Female patient from JAPAN , 82 years of age, was diagnosed with hypertension, constipation (What is constipation?), gastritis, insomnia and was treated with Amlodin (View Usage). After Amlodin was administered, patient had the following side effects: hepatitis fulminant. Amlodin dosage: . During the same period patient was treated with FORSENID (View Forsenid Review and Forsenid Label ), HOCHU EKKI TO (View Hochu-ekki-to Review and Hochu-ekki-to Label ), LENDORMIN D (View Lendormin D Review and Lendormin D Label ).

5267769-8 | Stevens-johnson Syndrome
on Mar 05, 2007 Female patient from JAPAN , 77 years of age, weighting 114.6 lb, was diagnosed with angina pectoris, rhinitis allergic, upper respiratory tract inflammation and was treated with Amlodin (View Usage). Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome. Amlodin dosage: . During the same period patient was treated with ONON (View Onon Review and Onon Label ), CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ), LOXONIN (View Loxonin Review and Loxonin Label ), FIRSTCIN (View Firstcin Review and Firstcin Label ).

5262696-4 | Musculoskeletal Pain, Pain In Extremity
Patient was taking Amlodin (View Usage). Patient had the following side effects: musculoskeletal pain, pain in extremity on Mar 01, 2007 from JAPAN Additional patient health information: Male patient , 76 years of age, was diagnosed with proteinuria and. Amlodin dosage: . During the same period patient was treated with METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), CIBENOL (View Cibenol Review and Cibenol Label ), TICLOPIDINE HYDROCHLORIDE (View Ticlopidine Hydrochloride Review and Ticlopidine Hydrochloride Label ), EPADEL (View Epadel Review and Epadel Label ), COZAAR (View Cozaar Review and Cozaar 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 Amlodin 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 Amlodin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Amlodin 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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Obsessive-compulsive disorder (OCD) is a type of anxiety disorder .

During the same period patient was treated with AMLODIN (2.5 Mg) (View Amlodin Review and Amlodin Label ), CALBLOCK ... (View Lodoz Review and Lodoz Label ), ZANIDIP ...

During the same period patient was treated with AMLODIN (View Amlodin Review and Amlodin Label ), TAKEPRON (View Takepron Review and Takepron Label ), LASIX (View Lasix Review ...

Label ), NEUFAN (View Neufan Review and Neufan Label ), AMLODIN OD (View Amlodin Od Review and Amlodin Od Label ), GOSHAJINKIGAN (View Goshajinkigan Review and ...

During the same period patient was treated with CLINORIL (View Clinoril Review and Clinoril Label ), TAMIFLU (View Tamiflu Review and Tamiflu Label ), AMLODIN (View Amlodin ...

During the same period patient was treated with DALACIN (1.8g Per Day) (View Dalacin Review and Dalacin Label ), AMLODIN (View Amlodin Review and Amlodin Label ), RIFADIN ...

Adalat Review and Adalat Label ), ALFAROL (View Alfarol Review and Alfarol Label ), AMLODIN OD (View Amlodin Od Review and Amlodin Od Label ), ASTAT (View Astat Review ...

During the same period patient was treated with AMLODIN (Unk) (View Amlodin Review and Amlodin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), URINORM (View ...

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Amlodin Reactions
Amniotic Cavity Disorder
Anaemia
Anorexia
Aspartate Aminotransferase Increased
Atrioventricular Block
Blood Alkaline Phosphatase Increased
Blood Creatine Phosphokinase Increased
Blood Creatinine Increased
Blood Potassium Decreased
Blood Potassium Increased
Blood Urea Increased
Bradycardia
Cardiac Failure
Cardio-respiratory Arrest
Dehydration
DizzinessWhat is Dizziness?
Dyspnoea
Femur Fracture
Haematocrit Decreased
Haemoglobin Decreased
HeadacheWhat is Headache?
Hyperglycaemia
Hypotension
Interstitial Lung Disease
NauseaWhat is Nausea?
Obsessive-compulsive DisorderWhat is Obsessive-compulsive disorder?
Overdose
Renal Disorder
Rhabdomyolysis
Vomiting
Amlodin 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 Amlodin 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!