PRINZIDE Side Effects

6971956-8 | Cough
on Sep 08, 2010 Female patient from UNITED STATES , 51 years of age, weighting 239.0 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: cough. Prinzide dosage: One Qd Po.

6939049-3 | Atrial Fibrillation, Contusion, Fatigue, Gastrointestinal Disorder, Headache, Injection Site Induration
Patient was taking Prinzide (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), contusion, fatigue, gastrointestinal disorder, headache (What is headache?), injection site induration on Aug 13, 2010 from UNITED STATES Additional patient health information: Female patient , 56 years of age, was diagnosed with thrombosis prophylaxis and. Prinzide dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), WARFARIN (View Warfarin Review and Warfarin Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ), DIGOXIN (View Digoxin Review and Digoxin Label ). Patient was hospitalized.

6700040-3 | Renal Failure
Adverse event was reported on Mar 20, 2009 by a Male patient taking Prinzide (View Usage) (Dosage: Po) . Location: UNITED STATES , 46 years of age, After Prinzide was administered, patient had the following side effects: renal failure. Patient was hospitalized.

6505931-4 | Interstitial Lung Disease
on Dec 09, 2009 Male patient from FRANCE , 85 years of age, was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Prinzide dosage: . During the same period patient was treated with ELISOR (View Elisor Review and Elisor Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), FELDENE (View Feldene Review and Feldene Label ), LASILIX (View Lasilix Review and Lasilix Label ).


6434736-8 | Syncope
on Nov 02, 2009 Female patient from GERMANY , 84 years of age, weighting 156.5 lb, was diagnosed with hypertension, infarction, prophylaxis, thrombosis prophylaxis and was treated with Prinzide (View Usage). Patient had the following side effects: syncope. Prinzide dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MOXONIDINE (View Moxonidine Review and Moxonidine Label ), NITRO SPRAY (View Nitro-spray Review and Nitro-spray Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LEVETIRACETAM (View Levetiracetam Review and Levetiracetam Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6286869-7 | Blood Calcium Decreased, Blood Sodium Decreased, Hypoglycaemia, Unresponsive To Stimuli
Patient was taking Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: blood calcium decreased, blood sodium decreased, hypoglycaemia, unresponsive to stimuli on Jul 17, 2009 from GERMANY Additional patient health information: Female patient , 74 years of age, was diagnosed with hypertension, type 2 diabetes mellitus and. Prinzide dosage: . During the same period patient was treated with BERLINSULIN H BASAL (View Berlinsulin H Basal Review and Berlinsulin H Basal Label ), ALPHAGAN (View Alphagan Review and Alphagan Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), THYRONAJOD (View Thyronajod Review and Thyronajod Label ). Patient was hospitalized.

6262807-8 | Bradycardia, Therapeutic Agent Toxicity
Adverse event was reported on Jul 02, 2009 by a Female patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with cardiac failure and. Location: SPAIN , 78 years of age, Patient experienced the following unwanted or unexpected effects: bradycardia, therapeutic agent toxicity. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), METFORMIN (View Metformin Review and Metformin Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ). Patient was hospitalized.

6213723-9 | Angioedema, Blood Glucose Increased, Dyspnoea, Fibrin D Dimer Increased, Haemoglobin Decreased, Pulmonary Mass, Throat Tightness, White Blood Cell Count Increased
on May 13, 2009 Male patient from UNITED STATES , 58 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Prinzide (View Usage). Patient had the following side effects: angioedema, blood glucose increased, dyspnoea, fibrin d dimer increased, haemoglobin decreased, pulmonary mass, throat tightness, white blood cell count increased. Prinzide dosage: Po. During the same period patient was treated with DAPAGLIFLOZIN (Po) (View Dapagliflozin Review and Dapagliflozin Label ), SINGULAIR (View Singulair Review and Singulair Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ). Patient was hospitalized.

6207438-0 | Angioedema, Blood Glucose Increased, Dyspnoea, Fibrin D Dimer Increased, Haemoglobin Decreased, Pulmonary Mass, Throat Tightness, White Blood Cell Count Increased
on May 13, 2009 Male patient from UNITED STATES , 58 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: angioedema, blood glucose increased, dyspnoea, fibrin d dimer increased, haemoglobin decreased, pulmonary mass, throat tightness, white blood cell count increased. Prinzide dosage: Po. During the same period patient was treated with DAPAGLIFLOZIN UNK (Po) (View Dapagliflozin Unk Review and Dapagliflozin Unk Label ), SINGULAIR (View Singulair Review and Singulair Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ). Patient was hospitalized.

6059254-0 | Syncope
Patient was taking Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: syncope on Jan 19, 2009 from GERMANY Additional patient health information: Female patient , 84 years of age, weighting 156.5 lb, was diagnosed with hypertension, infarction, prophylaxis, thrombosis prophylaxis and. Prinzide dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MOXONIDINE (View Moxonidine Review and Moxonidine Label ), NITRO SPRAY (View Nitro-spray Review and Nitro-spray Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LEVETIRACETAM (View Levetiracetam Review and Levetiracetam Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6049443-3 | Syncope
Adverse event was reported on Jan 13, 2009 by a Female patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: GERMANY , 84 years of age, Patient had the following side effects: syncope. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MOXONIDINE (View Moxonidine Review and Moxonidine Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LEVETIRACETAM (View Levetiracetam Review and Levetiracetam Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6039025-1 | Completed Suicide, Overdose
on Jan 05, 2009 Female patient from UNITED STATES , 49 years of age, was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: completed suicide, overdose. Prinzide dosage: Formulation: Tabs. During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ).

6035958-0 | Completed Suicide, Overdose
on Jan 05, 2009 Female patient from UNITED STATES , 49 years of age, was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: completed suicide, overdose. Prinzide dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ).

6034583-5 | Completed Suicide, Overdose
Patient was taking Prinzide (View Usage). Patient had the following side effects: completed suicide, overdose on Jan 05, 2009 from UNITED STATES Additional patient health information: Female patient , 49 years of age, . Prinzide dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ).

5927286-6 | Pancreatic Enzymes Increased
Adverse event was reported on Oct 17, 2008 by a Male patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with essential hypertension and. Location: SWITZERLAND , 56 years of age, After Prinzide was administered, patient had the following side effects: pancreatic enzymes increased.

5841969-8 | Anaemia, Benign Prostatic Hyperplasia, Blood Pressure Increased, Cellulitis, Confusional State, Delirium, Hypertension
on Jul 23, 2008 Male patient from UNITED STATES , 65 years of age, was diagnosed with hypersensitivity and was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, benign prostatic hyperplasia, blood pressure increased, cellulitis (What is cellulitis?), confusional state, delirium, hypertension. Prinzide dosage: . During the same period patient was treated with FLOMAX (MORNIFLUMATE) (View Flomax (morniflumate) Review and Flomax (morniflumate) Label ), CLARITIN (View Claritin Review and Claritin Label ), ACETAMINOPHEN AND HYDROCODONE BITARTRATE (View Acetaminophen And Hydrocodone Bitartrate Review and Acetaminophen And Hydrocodone Bitartrate Label ), PREVACID (View Prevacid Review and Prevacid Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), DILANTIN (View Dilantin Review and Dilantin Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

5835386-4 | Anaemia, Benign Prostatic Hyperplasia, Blood Pressure Increased, Cellulitis, Confusional State, Delirium, Hypertension
on Jul 23, 2008 Male patient from UNITED STATES , 65 years of age, was diagnosed with hypersensitivity and was treated with Prinzide (View Usage). Patient had the following side effects: anaemia, benign prostatic hyperplasia, blood pressure increased, cellulitis (What is cellulitis?), confusional state, delirium, hypertension. Prinzide dosage: . During the same period patient was treated with FLOMAX (MORNIFLUMATE) (View Flomax (morniflumate) Review and Flomax (morniflumate) Label ), CLARITIN (View Claritin Review and Claritin Label ), ACETAMINOPHEN AND HYDROCODONE BITARTRATE (View Acetaminophen And Hydrocodone Bitartrate Review and Acetaminophen And Hydrocodone Bitartrate Label ), PREVACID (View Prevacid Review and Prevacid Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), DILANTIN (View Dilantin Review and Dilantin Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

5822851-9 | Hypersensitivity
Patient was taking Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: hypersensitivity on Jun 26, 2008 from UNITED STATES Additional patient health information: Male patient , 60 years of age, . Prinzide dosage: 20/12.5 Mg Qd Po.

5742033-9 | Oral Intake Reduced, Renal Failure Acute
Adverse event was reported on May 13, 2008 by a Male patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with hypertension, hiv infection (What is hiv infection?), depression (What is depression?), benign prostatic hyperplasia, anxiety (What is anxiety?), gastrooesophageal reflux disease and. Location: UNITED STATES , 45 years of age, Patient experienced the following unwanted or unexpected effects: oral intake reduced, renal failure acute. During the same period patient was treated with KALETRA (View Kaletra Review and Kaletra Label ), VALACYCLOVIR HYDROCHLORIDE (View Valacyclovir Hydrochloride Review and Valacyclovir Hydrochloride Label ), TRUVADA (View Truvada Review and Truvada Label ), PAROXETINE HYDROCHLORIDE (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), PROSCAR (View Proscar Review and Proscar Label ), HYDROXYZINE PAMOATE (View Hydroxyzine Pamoate Review and Hydroxyzine Pamoate Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ). Patient was hospitalized.

5735026-9 | Gastrointestinal Disorder, Nausea, Palpitations, Stomach Discomfort
on May 05, 2008 Female patient from UNITED STATES , 56 years of age, weighting 152.1 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient had the following side effects: gastrointestinal disorder, nausea (What is nausea?), palpitations, stomach discomfort. Prinzide dosage: . Patient was hospitalized.

5711518-3 | Fatigue, Nephritis Interstitial, Oral Intake Reduced, Renal Tubular Necrosis
on Apr 07, 2008 Male patient from UNITED STATES , 44 years of age, was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: fatigue, nephritis interstitial, oral intake reduced, renal tubular necrosis. Prinzide dosage: . During the same period patient was treated with NADOLOL (View Nadolol Review and Nadolol Label ), LUNESTA (2 Week) (View Lunesta Review and Lunesta Label ), NORVASC (View Norvasc Review and Norvasc Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NEXIUM (View Nexium Review and Nexium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized.

5706399-8 | Nephritis Interstitial, Oral Intake Reduced, Renal Tubular Necrosis
Patient was taking Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: nephritis interstitial, oral intake reduced, renal tubular necrosis on Apr 07, 2008 from UNITED STATES Additional patient health information: Male patient , 44 years of age, . Prinzide dosage: . During the same period patient was treated with LUNESTA (View Lunesta Review and Lunesta Label ), NADOLOL (View Nadolol Review and Nadolol Label ), NEXIUM (View Nexium Review and Nexium Label ), NORVASC (View Norvasc Review and Norvasc Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LEXAPRO (View Lexapro Review and Lexapro Label ). Patient was hospitalized.

5563283-0 | Foetal Distress Syndrome, Hypotension, Oligohydramnios, Potter's Syndrome, Premature Baby, Small For Dates Baby
Adverse event was reported on Oct 18, 2007 by a Male patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: BELGIUM , weighting 4.41 lb, Patient had the following side effects: foetal distress syndrome, hypotension, oligohydramnios, potter's syndrome, premature baby, small for dates baby. During the same period patient was treated with PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ). Patient was hospitalized.

5532671-0 | Foetal Distress Syndrome, Hypotension, Oligohydramnios, Potter's Syndrome, Premature Baby, Small For Dates Baby
on Nov 26, 2007 Male patient from BELGIUM , weighting 4.41 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: foetal distress syndrome, hypotension, oligohydramnios, potter's syndrome, premature baby, small for dates baby. Prinzide dosage: . During the same period patient was treated with PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ). Patient was hospitalized.

5503075-1 | Foetal Distress Syndrome, Hypotension, Oligohydramnios, Potter's Syndrome, Premature Baby, Small For Dates Baby
on Oct 18, 2007 Male patient from BELGIUM , weighting 4.41 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: foetal distress syndrome, hypotension, oligohydramnios, potter's syndrome, premature baby, small for dates baby. Prinzide dosage: . During the same period patient was treated with PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ).

5478202-5 | Angioedema, Paraesthesia, Swollen Tongue, Throat Tightness
Patient was taking Prinzide (View Usage). Patient had the following side effects: angioedema, paraesthesia, swollen tongue, throat tightness on Apr 12, 2007 from UNITED STATES Additional patient health information: Female patient , 60 years of age, was diagnosed with hypertension and. Prinzide dosage: . During the same period patient was treated with IRBESARTAN (View Irbesartan Review and Irbesartan Label ), AVAPRO (View Avapro Review and Avapro Label ), DARVOCET (View Darvocet Review and Darvocet Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), RELAFEN (View Relafen Review and Relafen Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MINOXIDIL (View Minoxidil Review and Minoxidil Label ). Patient was hospitalized.

5404769-9 | Back Pain, Dehydration, Dizziness, Gait Disturbance, Presyncope, Pyrexia
Adverse event was reported on Jul 19, 2007 by a Male patient taking Prinzide (View Usage) (Dosage: Po) was diagnosed with hypertension, hepatitis c (What is hepatitis c?), blood pressure (What is blood pressure?) and. Location: UNITED STATES , 54 years of age, After Prinzide was administered, patient had the following side effects: back pain (What is back pain?), dehydration, dizziness (What is dizziness?), gait disturbance, presyncope, pyrexia. During the same period patient was treated with PEG INTRON (View Peg-intron Review and Peg-intron Label ), REBETOL (Po) (View Rebetol Review and Rebetol Label ). Patient was hospitalized.

5345113-5 | Cerebrovascular Accident
on Jun 23, 2006 Female patient from UNITED STATES , 60 years of age, was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident. Prinzide dosage: 20/12.5 Mg/daily/po. During the same period patient was treated with AGGRENOX (View Aggrenox Review and Aggrenox Label ), NORVASC (View Norvasc Review and Norvasc Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ).

5345109-3 | Angioedema
on Nov 10, 2006 Female patient from UNITED STATES , 54 years of age, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient had the following side effects: angioedema. Prinzide dosage: Po.

5304433-0 | Arthralgia, Back Pain, Epistaxis, Fall, Haemorrhage, Injury, International Normalised Ratio Increased, Pain In Extremity
Patient was taking Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: arthralgia, back pain (What is back pain?), epistaxis, fall (What is fall?), haemorrhage, injury, international normalised ratio increased, pain in extremity on Apr 12, 2007 from UNITED STATES Additional patient health information: Male patient , 74 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Prinzide dosage: . During the same period patient was treated with WARFARIN (2.5 Mg Daily; 5 Mg Weekly) (View Warfarin Review and Warfarin Label ), COUMADIN (View Coumadin Review and Coumadin Label ), CYTOMEL (View Cytomel Review and Cytomel Label ), LORTAB (View Lortab Review and Lortab Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ). Patient was hospitalized.

5254845-9 | Angioedema
Adverse event was reported on Mar 02, 2007 by a Female patient taking Prinzide (View Usage) (Dosage: Lisinopril 20mg/hctz 25mg Daily Po) was diagnosed with hypertension and. Location: UNITED STATES , 64 years of age, weighting 134.5 lb, Patient experienced the following unwanted or unexpected effects: angioedema. During the same period patient was treated with ZOCOR (View Zocor Review and Zocor Label ), NORVASC (View Norvasc Review and Norvasc Label ), ARICEPT (View Aricept Review and Aricept Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ). Patient was hospitalized.

5174829-9 | Face Oedema, Lip Oedema
on Dec 05, 2006 Male patient from PORTUGAL , 70 years of age, weighting 209.4 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient had the following side effects: face oedema, lip oedema. Prinzide dosage: .

5155837-0 | Hypertension, Oedema, Swollen Tongue
on Nov 20, 2006 Female patient from UNITED STATES , weighting 202.0 lb, was diagnosed with hypertension and was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: hypertension, oedema, swollen tongue. Prinzide dosage: 1 Tablet Daily Po. Patient was hospitalized.

5071855-5 | Pityriasis Rosea
Patient was taking Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: pityriasis rosea on Jul 13, 2006 from ITALY Additional patient health information: Female patient , 74 years of age, . Prinzide dosage: Po. Patient was hospitalized.

5005454-8 | Cardiac Murmur, Cerebrovascular Accident, Hypercholesterolaemia, Lacunar Infarction, Neck Pain
Adverse event was reported on Mar 23, 2006 by a Female patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?), back pain (What is back pain?) and. Location: UNITED STATES , 66 years of age, weighting 145.5 lb, Patient had the following side effects: cardiac murmur, cerebrovascular accident, hypercholesterolaemia, lacunar infarction, neck pain. During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), SEREVENT (View Serevent Review and Serevent Label ), FLOVENT (View Flovent Review and Flovent Label ), MEPREDNISONE (View Meprednisone Review and Meprednisone Label ), PRINIVIL (View Prinivil Review and Prinivil Label ), ZITHROMAX (View Zithromax Review and Zithromax Label ). Patient was hospitalized and became disabled.

4999643-6 | Cerebrovascular Accident
on Mar 23, 2006 Female patient from UNITED STATES , 66 years of age, weighting 145.5 lb, was diagnosed with arthritis (What is arthritis?), back pain (What is back pain?) and was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: cerebrovascular accident. Prinzide dosage: . During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), SEREVENT (View Serevent Review and Serevent Label ), FLOVENT (View Flovent Review and Flovent Label ), MEPREDNISONE (View Meprednisone Review and Meprednisone Label ), PRINIVIL (View Prinivil Review and Prinivil Label ), ZITHROMAX (View Zithromax Review and Zithromax Label ).

4901971-7 | Blood Pressure Systolic Increased
on Feb 01, 2006 Male patient from UNITED STATES , 60 years of age, weighting 192.0 lb, was diagnosed with cardiovascular disorder, hypertension and was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure systolic increased. Prinzide dosage: 20/25 Mg Po. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PLAVIX (View Plavix Review and Plavix Label ), NORVASC (View Norvasc Review and Norvasc Label ), LOTENSIN (View Lotensin Review and Lotensin Label ).

4860565-2 | Angioneurotic Oedema, Colon Cancer, Dysphagia, Oedema Mouth, Swollen Tongue
Patient was taking Prinzide (View Usage). Patient had the following side effects: angioneurotic oedema, colon cancer, dysphagia, oedema mouth, swollen tongue on Jul 19, 2005 from UNITED STATES Additional patient health information: Female patient , 74 years of age, weighting 114.6 lb, was diagnosed with hypertension, osteoporosis (What is osteoporosis?), hyperlipidaemia and. Prinzide dosage: . During the same period patient was treated with FOSAMAX (View Fosamax Review and Fosamax Label ), ZOCOR (View Zocor Review and Zocor Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LEVAQUIN (View Levaquin Review and Levaquin Label ), PROTONIX (View Protonix Review and Protonix Label ), ETODOLAC (View Etodolac Review and Etodolac Label ).

4775636-9 | Dyspnoea, Swollen Tongue
Adverse event was reported on Sep 20, 2005 by a Male patient taking Prinzide (View Usage) (Dosage: Daily) was diagnosed with hypertension and. Location: UNITED STATES , 64 years of age, After Prinzide was administered, patient had the following side effects: dyspnoea, swollen tongue. Patient was hospitalized.

4750569-2 | Bronchitis, Bronchospasm, Herpes Simplex, Influenza, Laryngeal Oedema, Obstructive Airways Disorder, Rash
on May 16, 2005 Male patient from UNITED STATES , 49 years of age, weighting 160.9 lb, was treated with Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: bronchitis (What is bronchitis?), bronchospasm, herpes simplex (What is herpes simplex?), influenza, laryngeal oedema, obstructive airways disorder, rash (What is rash?). Prinzide dosage: . During the same period patient was treated with SINGULAIR (View Singulair Review and Singulair Label ), FLOVENT (View Flovent Review and Flovent Label ), ALLEGRA (View Allegra Review and Allegra Label ), PROVENTIL (View Proventil Review and Proventil Label ).

4704706-6 | Angioneurotic Oedema, Convulsion
on Jun 27, 2005 Female patient from , 83 years of age, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient had the following side effects: angioneurotic oedema, convulsion. Prinzide dosage: .

4675136-0 | Bronchitis, Influenza, Laryngeal Oedema, Obstructive Airways Disorder
Patient was taking Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: bronchitis (What is bronchitis?), influenza, laryngeal oedema, obstructive airways disorder on May 16, 2005 from Additional patient health information: Male patient , 49 years of age, . Prinzide dosage: .

4655798-4 | Blood Pressure Increased
Adverse event was reported on Apr 28, 2005 by a Male patient taking Prinzide (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: , 68 years of age, weighting 145.5 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased. During the same period patient was treated with HYDROCHLOROTHIAZIDE AND LISINOPRIL (View Hydrochlorothiazide And Lisinopril Review and Hydrochlorothiazide And Lisinopril Label ).

4654249-3 | Anaphylactoid Reaction, Angioneurotic Oedema, Cerumen Impaction
on Apr 25, 2005 Male patient from , 64 years of age, was diagnosed with hypertension and was treated with Prinzide (View Usage). Patient had the following side effects: anaphylactoid reaction, angioneurotic oedema, cerumen impaction. Prinzide dosage: .

4650520-X | Angioneurotic Oedema
on Apr 25, 2005 Male patient from , 60 years of age, was diagnosed with hypertension and was treated with Prinzide (View Usage). After Prinzide was administered, patient had the following side effects: angioneurotic oedema. Prinzide dosage: .

4575480-1 | Confusional State, Vertigo
Patient was taking Prinzide (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, vertigo on Jan 28, 2005 from Additional patient health information: Female patient , 81 years of age, weighting 142.0 lb, was diagnosed with hypertension and. Prinzide dosage: 10-12.5 Mg 1 Po Daily Lifetime.