ALTEIS Side Effects

5228631-X | Dry Mouth, Malaise, Tachyarrhythmia
on Jan 17, 2007 Female patient from FRANCE , 61 years of age, was diagnosed with hypertension and was treated with Alteis (View Usage). Patient experienced the following unwanted or unexpected effects: dry mouth, malaise, tachyarrhythmia. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Qd Po) (View Fludex Review and Fludex Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ).

5086047-3 | Gastric Ulcer Perforation, Hyperkalaemia, Myoglobinaemia, Neutrophil Percentage Increased, Peritonitis, Platelet Count Increased, Renal Failure Acute, Septic Shock, White Blood Cell Count Increased
Patient was taking Alteis (View Usage). Patient had the following side effects: gastric ulcer perforation, hyperkalaemia, myoglobinaemia, neutrophil percentage increased, peritonitis, platelet count increased, renal failure acute, septic shock, white blood cell count increased on Aug 03, 2006 from FRANCE Additional patient health information: Female patient , 55 years of age, weighting 273.4 lb, was diagnosed with essential hypertension, musculoskeletal pain and. Alteis dosage: 10 Mg Qd Po. During the same period patient was treated with SEROPRAM (View Seropram Review and Seropram Label ), DAFALGAN CODEINE (View Dafalgan Codeine Review and Dafalgan Codeine Label ), PLAVIX (75 Mg Daily Po) (View Plavix Review and Plavix Label ), PARIET (View Pariet Review and Pariet Label ), BUFLOMEDIL (View Buflomedil Review and Buflomedil Label ). Patient was hospitalized.

5062292-8 | Anaphylactic Reaction, Angioneurotic Oedema, Respiratory Disorder
Adverse event was reported on Jul 10, 2006 by a Female patient taking Alteis (View Usage) (Dosage: 10 Mg Qd Po) was diagnosed with essential hypertension and. Location: FRANCE , 78 years of age, After Alteis was administered, patient had the following side effects: anaphylactic reaction, angioneurotic oedema, respiratory disorder. Patient was hospitalized.

4831022-4 | Acute Febrile Neutrophilic Dermatosis, Myalgia
on Nov 02, 2005 Male patient from FRANCE , 62 years of age, was diagnosed with hypertension and was treated with Alteis (View Usage). Patient experienced the following unwanted or unexpected effects: acute febrile neutrophilic dermatosis, myalgia. Alteis dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ). Patient was hospitalized.


4693762-X | Abdominal Pain, Blood Sodium Decreased, Constipation, Syncope Vasovagal
on Jun 06, 2005 Female patient from , 74 years of age, was diagnosed with essential hypertension, depression (What is depression?) and was treated with Alteis (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), blood sodium decreased, constipation (What is constipation?), syncope vasovagal. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Po) (View Fludex Review and Fludex Label ), TEMESTA (View Temesta Review and Temesta Label ), ZOCOR (View Zocor Review and Zocor Label ), NORSET (60 Mg Po) (View Norset Review and Norset Label ). Patient was hospitalized.

4674004-8 | Abdominal Pain, Constipation, Depression, Hypercholesterolaemia, Hyponatraemia, Syncope Vasovagal
Patient was taking Alteis (View Usage). After Alteis was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), constipation (What is constipation?), depression (What is depression?), hypercholesterolaemia, hyponatraemia, syncope vasovagal on May 12, 2005 from Additional patient health information: Female patient , 74 years of age, was diagnosed with essential hypertension, depression (What is depression?) and. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Po) (View Fludex Review and Fludex Label ), NORSET (60 Mg Po) (View Norset Review and Norset Label ), TEMESTA (View Temesta Review and Temesta Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

4640603-2 | Chest Discomfort, Dyspnoea Paroxysmal Nocturnal
Adverse event was reported on Apr 06, 2005 by a Female patient taking Alteis (View Usage) (Dosage: 20 Mg Qd Po) was diagnosed with essential hypertension and. Location: , 54 years of age, Patient experienced the following unwanted or unexpected effects: chest discomfort, dyspnoea paroxysmal nocturnal.

4607427-3 | Amnesia, Insomnia, Malaise, Road Traffic Accident
on Feb 25, 2005 Male patient from , 54 years of age, was diagnosed with essential hypertension and was treated with Alteis (View Usage). Patient had the following side effects: amnesia, insomnia, malaise, road traffic accident. Alteis dosage: 10 Mg Qd Po. Patient was hospitalized.