NISIS Side Effects

6921380-9 | Blood Bilirubin Increased, Confusional State, Depressed Level Of Consciousness, Encephalopathy, Obsessive Thoughts
on Jul 28, 2010 Male patient from FRANCE , 71 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: blood bilirubin increased, confusional state, depressed level of consciousness, encephalopathy, obsessive thoughts. Nisis dosage: One Dosage Form (160 Mg) Daily. During the same period patient was treated with VISKEN (Unk) (View Visken Review and Visken Label ), BOOSTRIX (DIPHTH.+TETANUS+PERTUS.TOXOID/B.PERTUS.FILA.HAEM./PERTACTIN) (One Injection) (View Boostrix (diphth.+tetanus+pertus.toxoid/b.pertus.fila.haem./pertactin) Review and Boostrix (diphth.+tetanus+pertus.toxoid/b.pertus.fila.haem./pertactin) Label ), FUCIDINE CAP (250 Mg) (View Fucidine Cap Review and Fucidine Cap Label ). Patient was hospitalized.

6742112-3 | Blood Pressure Increased, Paradoxical Pressor Response
Patient was taking Nisis (View Usage). Patient had the following side effects: blood pressure increased, paradoxical pressor response on May 21, 2010 from FRANCE Additional patient health information: Female patient , weighting 134.5 lb, was diagnosed with hypertension and. Nisis dosage: 160 Mg, Qd. During the same period patient was treated with LODOZ (10 Mg) (View Lodoz Review and Lodoz Label ), HYPERIUM (View Hyperium Review and Hyperium Label ).

6674996-1 | Acute Pulmonary Oedema, Cerebral Hypoperfusion, Hyperkalaemia, Hyponatraemia, Hypotension, Hypovolaemic Shock, Renal Failure Acute
Adverse event was reported on Oct 12, 2009 by a Female patient taking Nisis (View Usage) (Dosage: Daily Dose: 40 Milligram(s)) was diagnosed with hypertension and. Location: FRANCE , 87 years of age, After Nisis was administered, patient had the following side effects: acute pulmonary oedema, cerebral hypoperfusion, hyperkalaemia, hyponatraemia, hypotension, hypovolaemic shock, renal failure acute. During the same period patient was treated with COVERSYL NOS (View Coversyl Nos Review and Coversyl Nos Label ). Patient was hospitalized.

6424595-1 | Cough, Dyspnoea, Epistaxis, Erysipelas, Oedema, Respiratory Disorder, Weight Increased
on Oct 20, 2009 Male patient from FRANCE , 78 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: cough, dyspnoea, epistaxis, erysipelas, oedema, respiratory disorder, weight increased. Nisis dosage: 160 Mg, Qd. During the same period patient was treated with NISISCO (1 Tablet (160/12.5 Mg)) (View Nisisco Review and Nisisco Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ).


6415303-9 | Acute Pulmonary Oedema, Blood Creatinine Increased, Cerebral Hypoperfusion, Dehydration, Fall, Hyperkalaemia, Hyponatraemia, Hypotension, Hypovolaemic Shock
on Oct 14, 2009 Female patient from FRANCE , 87 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). Patient had the following side effects: acute pulmonary oedema, blood creatinine increased, cerebral hypoperfusion, dehydration, fall (What is fall?), hyperkalaemia, hyponatraemia, hypotension, hypovolaemic shock. Nisis dosage: 40 Mg, Qd. During the same period patient was treated with COVERSYL (Unk) (View Coversyl Review and Coversyl Label ). Patient was hospitalized.

6264039-6 | Amnesia, Fall, Haematoma, Loss Of Consciousness, Wound
Patient was taking Nisis (View Usage). After Nisis was administered, patient had the following side effects: amnesia, fall (What is fall?), haematoma, loss of consciousness, wound (What is wound?) on Jun 26, 2009 from FRANCE Additional patient health information: Female patient , 65 years of age, was diagnosed with hypertension and. Nisis dosage: 160 Mg Daily. During the same period patient was treated with FLUDEX (Unk) (View Fludex Review and Fludex Label ). Patient was hospitalized.

6164213-3 | Alanine Aminotransferase Increased, Asthenia, Chromaturia, Eosinophil Count Increased, Haemoglobin Decreased, Haemolytic Anaemia, Jaundice, Reticulocytosis, Serum Ferritin Increased
Adverse event was reported on Mar 24, 2009 by a Male patient taking Nisis (View Usage) (Dosage: 40 Mg, Qd) was diagnosed with hypertension, rhinorrhoea, sleep apnoea syndrome and. Location: FRANCE , weighting 220.5 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, asthenia, chromaturia, eosinophil count increased, haemoglobin decreased, haemolytic anaemia, jaundice (What is jaundice?), reticulocytosis, serum ferritin increased. During the same period patient was treated with DOLI RHUME (Unk) (View Doli Rhume Review and Doli Rhume Label ), DOMPERIDONE (30 Mg) (View Domperidone Review and Domperidone Label ), TETANUS VACCINE /00052801/ (Unk) (View Tetanus Vaccine /00052801/ Review and Tetanus Vaccine /00052801/ Label ), FERVEX (View Fervex Review and Fervex Label ), CONTINUOUS POSITIVE AIRWAY PRESSURE (View Continuous Positive Airway Pressure Review and Continuous Positive Airway Pressure Label ), OROCAL D3 (1 Df, Qd) (View Orocal D3 Review and Orocal D3 Label ), SPECIAFOLDINE (5 Mg, Bid) (View Speciafoldine Review and Speciafoldine Label ), FOSAMAX (1 Df, Qw) (View Fosamax Review and Fosamax Label ). Patient was hospitalized.

6146395-2 | Alanine Aminotransferase Increased, Blood Bilirubin Unconjugated Increased, Chromaturia, Eosinophil Count Increased, Haemolytic Anaemia, Reticulocyte Count Increased, Serum Ferritin Increased
on Mar 24, 2009 Male patient from FRANCE , 60 years of age, was diagnosed with hypertension, rhinorrhoea, tetanus immunisation, myalgia, sleep apnoea syndrome and was treated with Nisis (View Usage). Patient had the following side effects: alanine aminotransferase increased, blood bilirubin unconjugated increased, chromaturia, eosinophil count increased, haemolytic anaemia, reticulocyte count increased, serum ferritin increased. Nisis dosage: . During the same period patient was treated with DOLI RHUME (View Doli Rhume Review and Doli Rhume Label ), DOMPERIDONE (10 Mg, Tid) (View Domperidone Review and Domperidone Label ), TETANUS VACCINE (View Tetanus Vaccine Review and Tetanus Vaccine Label ), NIFLURIL (Unk, Unk) (View Nifluril Review and Nifluril Label ), CONTINUOUS POSITIVE AIRWAY PRESSURE (View Continuous Positive Airway Pressure Review and Continuous Positive Airway Pressure Label ). Patient was hospitalized.

6144866-6 | Alanine Aminotransferase Increased, Asthenia, Chromaturia, Eosinophil Count Increased, Haemoglobin Decreased, Haemolytic Anaemia, Jaundice, Reticulocytosis, Serum Ferritin Increased
on Mar 24, 2009 Male patient from FRANCE , weighting 220.5 lb, was diagnosed with hypertension, rhinorrhoea, sleep apnoea syndrome and was treated with Nisis (View Usage). After Nisis was administered, patient had the following side effects: alanine aminotransferase increased, asthenia, chromaturia, eosinophil count increased, haemoglobin decreased, haemolytic anaemia, jaundice (What is jaundice?), reticulocytosis, serum ferritin increased. Nisis dosage: 40 Mg, Qd. During the same period patient was treated with DOLI RHUME (Unk) (View Doli Rhume Review and Doli Rhume Label ), FERVEX (View Fervex Review and Fervex Label ), CONTINUOUS POSITIVE AIRWAY PRESSURE (View Continuous Positive Airway Pressure Review and Continuous Positive Airway Pressure Label ). Patient was hospitalized.

5712428-8 | Blood Pressure Decreased, Intentional Overdose, Suicide Attempt
Patient was taking Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, intentional overdose, suicide attempt on Apr 11, 2008 from FRANCE Additional patient health information: Female patient , 70 years of age, was diagnosed with suicide attempt and. Nisis dosage: 1600 Mg, Once/single. Patient was hospitalized.

5708548-4 | Coma, Hyperkalaemia, Renal Failure Acute
Adverse event was reported on Apr 08, 2008 by a Male patient taking Nisis (View Usage) (Dosage: 80 Mg, Qd) was diagnosed with hypertension and. Location: FRANCE , 70 years of age, Patient had the following side effects: coma, hyperkalaemia, renal failure acute. Patient was hospitalized.

5636334-2 | Alanine Aminotransferase Increased, Asthenia, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Glucose Increased, Gamma-glutamyltransferase Increased, Hepatitis, Jaundice
on Feb 14, 2008 Female patient from FRANCE , 74 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). After Nisis was administered, patient had the following side effects: alanine aminotransferase increased, asthenia, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood glucose increased, gamma-glutamyltransferase increased, hepatitis (What is hepatitis?), jaundice (What is jaundice?). Nisis dosage: 80 Mg, Qd. Patient was hospitalized.

5626006-2 | Acidosis, Anaemia, Blood Creatinine Increased, Blood Folate Decreased, C-reactive Protein Increased, Creatinine Renal Clearance Decreased, Fall, Haemoconcentration
on Feb 05, 2008 Female patient from FRANCE , 80 years of age, was diagnosed with hypertensive cardiomyopathy, infection (What is infection?), insomnia, dyslipidaemia, depression (What is depression?), gastrooesophageal reflux disease, hypothyroidism and was treated with Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: acidosis, anaemia, blood creatinine increased, blood folate decreased, c-reactive protein increased, creatinine renal clearance decreased, fall (What is fall?), haemoconcentration. Nisis dosage: . During the same period patient was treated with BACTRIM (2 Df, Qd) (View Bactrim Review and Bactrim Label ), HAVLANE (1 Df, Qd) (View Havlane Review and Havlane Label ), ALDALIX (1 Df, Qd) (View Aldalix Review and Aldalix Label ), LIPANTHYL (160 Mg, Qd) (View Lipanthyl Review and Lipanthyl Label ), ATHYMIL (10 Mg, Qd) (View Athymil Review and Athymil Label ), INIPOMP (20 Mg, Qd) (View Inipomp Review and Inipomp Label ), LEVOTHYROX (150 Ug, Qd) (View Levothyrox Review and Levothyrox Label ). Patient was hospitalized.

5572853-5 | Altered State Of Consciousness, Blood Glucose Increased, Brain Herniation, Circulatory Collapse, Confusional State, International Normalised Ratio Increased, Monoparesis, Subarachnoid Haemorrhage, Subdural Haematoma
Patient was taking Nisis (View Usage). Patient had the following side effects: altered state of consciousness, blood glucose increased, brain herniation, circulatory collapse, confusional state, international normalised ratio increased, monoparesis, subarachnoid haemorrhage, subdural haematoma on Dec 19, 2007 from FRANCE Additional patient health information: Female patient , 75 years of age, was diagnosed with hypertension, atrial fibrillation (What is atrial fibrillation?), hypercholesterolaemia and. Nisis dosage: 1 Df, Qd. During the same period patient was treated with PREVISCAN (0.75 Tab One Day / 0.5 Tab The Following Day) (View Previscan Review and Previscan Label ), ZOCOR (View Zocor Review and Zocor Label ), ACARBOSE (View Acarbose Review and Acarbose Label ), HEMIGOXINE (View Hemigoxine Review and Hemigoxine Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), NOOTROPYL (View Nootropyl Review and Nootropyl Label ). Patient was hospitalized.

5309348-X | Blood Iron Decreased, Gastritis Atrophic, Gastrointestinal Haemorrhage, Haematocrit Decreased, Haemoglobin Decreased, Iron Deficiency Anaemia, Red Blood Cell Count Decreased, Serum Ferritin Decreased
Adverse event was reported on Apr 16, 2007 by a Female patient taking Nisis (View Usage) (Dosage: 160 Mg, Qd) was diagnosed with hypertension and. Location: FRANCE , 79 years of age, weighting 94.80 lb, After Nisis was administered, patient had the following side effects: blood iron decreased, gastritis atrophic, gastrointestinal haemorrhage, haematocrit decreased, haemoglobin decreased, iron deficiency anaemia, red blood cell count decreased, serum ferritin decreased. During the same period patient was treated with CORDARONE (100 Mg) (View Cordarone Review and Cordarone Label ), HYPERIUM (2 Mg) (View Hyperium Review and Hyperium Label ), DAFALGAN (1500 Mg) (View Dafalgan Review and Dafalgan Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ).

5176710-8 | Blood Pressure Decreased, Circulatory Collapse, Multi-organ Failure, Suicide Attempt
on Dec 14, 2006 Male patient from FRANCE , 69 years of age, was treated with Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, circulatory collapse, multi-organ failure, suicide attempt. Nisis dosage: . During the same period patient was treated with ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), TRICYCLIC ANTIDEPRESSANTS (View Tricyclic Antidepressants Review and Tricyclic Antidepressants Label ). Patient was hospitalized.

5079487-X | Asthenia, Chromaturia, Haemoglobin Decreased, Haemolytic Anaemia, Jaundice
on Jun 14, 2006 Male patient from FRANCE , 60 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). Patient had the following side effects: asthenia, chromaturia, haemoglobin decreased, haemolytic anaemia, jaundice (What is jaundice?). Nisis dosage: 40 Mg, Qd. During the same period patient was treated with FERVEX (View Fervex Review and Fervex Label ). Patient was hospitalized.

5019117-6 | Blood Creatinine Increased, Blood Urea Increased, Hyperkalaemia, Lactic Acidosis, Renal Failure Acute
Patient was taking Nisis (View Usage). After Nisis was administered, patient had the following side effects: blood creatinine increased, blood urea increased, hyperkalaemia, lactic acidosis, renal failure acute on May 29, 2006 from FRANCE Additional patient health information: Male patient , 71 years of age, was diagnosed with hypertension, diabetes mellitus and. Nisis dosage: 160 Mg, Qd. During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ). Patient was hospitalized.

4971493-6 | Agitation, Blood Thyroid Stimulating Hormone Increased, Confusional State, Hypothyroidism
Adverse event was reported on Apr 06, 2006 by a Female patient taking Nisis (View Usage) (Dosage: ) . Location: FRANCE , 91 years of age, Patient experienced the following unwanted or unexpected effects: agitation, blood thyroid stimulating hormone increased, confusional state, hypothyroidism. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), BUFLOMEDIL (View Buflomedil Review and Buflomedil Label ), PREVISCAN (20 Mg/day) (View Previscan Review and Previscan Label ), CORDARONE (200 Mg/day) (View Cordarone Review and Cordarone Label ), EFFEXOR (37.5 Mg/day) (View Effexor Review and Effexor Label ). Patient was hospitalized.

4944695-2 | Asthma, Cough, Nasopharyngitis, Rhinitis Allergic, Sneezing, Throat Irritation
on Mar 03, 2006 Female patient from FRANCE , 72 years of age, was diagnosed with hypertension, thyroidectomy and was treated with Nisis (View Usage). Patient had the following side effects: asthma (What is asthma?), cough, nasopharyngitis, rhinitis allergic, sneezing, throat irritation. Nisis dosage: 80 Mg, Qd. During the same period patient was treated with TAHOR (1 Df, Qd) (View Tahor Review and Tahor Label ), CYNOMEL (View Cynomel Review and Cynomel Label ).

4846629-8 | Infertility Male, Sperm Count Decreased
on Nov 25, 2005 Male patient from FRANCE , 38 years of age, was diagnosed with hypertension and was treated with Nisis (View Usage). After Nisis was administered, patient had the following side effects: infertility male, sperm count decreased. Nisis dosage: 80 Mg, Qd.

4845516-9 | Drop Attacks, Road Traffic Accident, Somnolence
Patient was taking Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: drop attacks, road traffic accident, somnolence on Feb 07, 2003 from FRANCE Additional patient health information: Male patient , 58 years of age, weighting 180.8 lb, was diagnosed with hypertension and. Nisis dosage: 80 Mg/day. During the same period patient was treated with ELISOR (View Elisor Review and Elisor Label ).

4740547-1 | Habitual Abortion
Adverse event was reported on Aug 04, 2005 by a Female patient taking Nisis (View Usage) (Dosage: 80 Mg/day) . Location: FRANCE , 37 years of age, weighting 253.5 lb, Patient had the following side effects: habitual abortion.

4656732-3 | Congenital Pulmonary Hypertension, Hydrops Foetalis, Limb Malformation, Neonatal Hypoxia, Premature Baby, Renal Failure Neonatal
on May 03, 2005 Female patient from , weighting 4.41 lb, was treated with Nisis (View Usage). After Nisis was administered, patient had the following side effects: congenital pulmonary hypertension, hydrops foetalis, limb malformation, neonatal hypoxia, premature baby, renal failure neonatal. Nisis dosage: Unk, Unk.

4607552-7 | Abnormal Behaviour, Atrioventricular Block Second Degree, Cardiac Pacemaker Insertion, Fall
on Mar 08, 2005 Male patient from , 87 years of age, was diagnosed with essential hypertension, benign prostatic hyperplasia, diabetes mellitus non-insulin-dependent and was treated with Nisis (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, atrioventricular block second degree, cardiac pacemaker insertion, fall (What is fall?). Nisis dosage: 80 Mg, Qd. During the same period patient was treated with TRANDATE (200 Mg, Qd) (View Trandate Review and Trandate Label ), PROSCAR (View Proscar Review and Proscar Label ), GLUCOR (View Glucor Review and Glucor Label ), EQUANIL (View Equanil Review and Equanil Label ). Patient was hospitalized.

4590306-8 | Haemoglobin Decreased, Malaise, Normochromic Normocytic Anaemia, Oedema
Patient was taking Nisis (View Usage). Patient had the following side effects: haemoglobin decreased, malaise, normochromic normocytic anaemia, oedema on Feb 16, 2005 from Additional patient health information: Male patient , 57 years of age, was diagnosed with oedema and. Nisis dosage: 80 Mg, Qd. During the same period patient was treated with ESIDRIX (View Esidrix Review and Esidrix Label ), LASILIX (60 Mg/day) (View Lasilix Review and Lasilix Label ), EQUANIL (400 Mg/day) (View Equanil Review and Equanil Label ). Patient was hospitalized.