MINIPRESS Side Effects

7002441-5 | Cough, Syncope
on Feb 20, 2009 Male patient from FRANCE , 57 years of age, was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: cough, syncope. Minipress dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), FLUDEX (View Fludex Review and Fludex Label ), IPERTEN (View Iperten Review and Iperten Label ). Patient was hospitalized.

6806393-X | Chills, Nasopharyngitis
Patient was taking Minipress (View Usage). Patient had the following side effects: chills, nasopharyngitis on Feb 26, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 205.0 lb, was diagnosed with prostatomegaly and. Minipress dosage: . During the same period patient was treated with ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ).

6750226-7 | Dizziness, Gait Disturbance, Periorbital Oedema
Adverse event was reported on May 21, 2010 by a Female patient taking Minipress (View Usage) (Dosage: 6 Mg, 1x/day) was diagnosed with hypertension and. Location: MALAYSIA , 51 years of age, After Minipress was administered, patient had the following side effects: dizziness (What is dizziness?), gait disturbance, periorbital oedema. During the same period patient was treated with BUDESONIDE (View Budesonide Review and Budesonide Label ), TELMISARTAN (View Telmisartan Review and Telmisartan Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6750214-0 | Chest Pain, Headache, Vision Blurred
on May 21, 2010 Female patient from MALAYSIA , 61 years of age, was diagnosed with hypertension and was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), headache (What is headache?), vision blurred. Minipress dosage: 3 Mg, 1x/day.


6003927-2 | Blood Pressure Fluctuation, Dizziness, Heart Rate Decreased, Nausea
on Dec 05, 2008 Female patient from INDIA , 75 years of age, was treated with Minipress (View Usage). Patient had the following side effects: blood pressure fluctuation, dizziness (What is dizziness?), heart rate decreased, nausea (What is nausea?). Minipress dosage: 2.5 Mg, 1x/day. During the same period patient was treated with CARDACE (View Cardace Review and Cardace Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), DITIDE (View Ditide Review and Ditide Label ).

5921014-6 | Dizziness, Headache, Lethargy, Syncope
Patient was taking Minipress (View Usage). After Minipress was administered, patient had the following side effects: dizziness (What is dizziness?), headache (What is headache?), lethargy, syncope on Oct 06, 2008 from MALAYSIA Additional patient health information: Female patient , 42 years of age, was diagnosed with hypertension and. Minipress dosage: Daily Dose:15mg-text:15 Mg-freq:daily. During the same period patient was treated with FRUSEMIDE (View Frusemide Review and Frusemide Label ), TRIMETAZIDINE (View Trimetazidine Review and Trimetazidine Label ), METHYLDOPA (View Methyldopa Review and Methyldopa Label ).

5760420-X | Hypoglycaemia
Adverse event was reported on May 26, 2008 by a Male patient taking Minipress (View Usage) (Dosage: ) was diagnosed with diabetes mellitus and. Location: AUSTRALIA , 66 years of age, Patient experienced the following unwanted or unexpected effects: hypoglycaemia. During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), LASIX (View Lasix Review and Lasix Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5733789-X | Abdominal Discomfort, Hallucination, Visual, Myopia, Tongue Coated, Urinary Incontinence, Vision Blurred, Weight Increased
on Apr 29, 2008 Female patient from AUSTRALIA , 72 years of age, was diagnosed with hypertension and was treated with Minipress (View Usage). Patient had the following side effects: abdominal discomfort, hallucination, visual, myopia, tongue coated, urinary incontinence (What is urinary incontinence?), vision blurred, weight increased. Minipress dosage: . During the same period patient was treated with ATACAND (View Atacand Review and Atacand Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ).

5708569-1 | Dizziness, Headache, Lethargy, Syncope
on Apr 07, 2008 Female patient from MALAYSIA , 42 years of age, was diagnosed with hypertension and was treated with Minipress (View Usage). After Minipress was administered, patient had the following side effects: dizziness (What is dizziness?), headache (What is headache?), lethargy, syncope. Minipress dosage: Daily Dose:15mg-text:15 Mg-freq:daily. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), TRIMETAZIDINE (View Trimetazidine Review and Trimetazidine Label ), METHYLDOPA (View Methyldopa Review and Methyldopa Label ).

5656068-8 |
Patient was taking Minipress (View Usage). on Feb 26, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 140.0 lb, was diagnosed with pain (What is pain?) and. Minipress dosage: . During the same period patient was treated with ANALGESICS (View Analgesics Review and Analgesics Label ).

5473900-1 | Floppy Iris Syndrome
Adverse event was reported on Sep 20, 2007 by a Male patient taking Minipress (View Usage) (Dosage: ) . Location: JAPAN , 71 years of age, Patient had the following side effects: floppy iris syndrome. During the same period patient was treated with HARNAL (View Harnal Review and Harnal Label ), LANIRAPID (View Lanirapid Review and Lanirapid Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LASIX (View Lasix Review and Lasix Label ), KARY UNI (View Kary Uni Review and Kary Uni Label ).

5290830-9 | Sjogren's Syndrome, Thirst
on Mar 30, 2007 Female patient from JAPAN , 75 years of age, was diagnosed with hypertension and was treated with Minipress (View Usage). After Minipress was administered, patient had the following side effects: sjogren's syndrome (What is sjogren's syndrome?), thirst. Minipress dosage: Daily Dose:.5mg. During the same period patient was treated with BLOPRESS (View Blopress Review and Blopress Label ), AMLODIN (View Amlodin Review and Amlodin Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ), DASEN (View Dasen Review and Dasen Label ), DEZOLAM (View Dezolam Review and Dezolam Label ), MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5285354-9 | Sjogren's Syndrome, Thirst
on Mar 23, 2007 Female patient from JAPAN , 75 years of age, was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: sjogren's syndrome (What is sjogren's syndrome?), thirst. Minipress dosage: Daily Dose:.5mg. During the same period patient was treated with BLOPRESS (View Blopress Review and Blopress Label ), AMLODIN (View Amlodin Review and Amlodin Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ), DASEN (View Dasen Review and Dasen Label ), DEZOLAM (View Dezolam Review and Dezolam Label ), MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5212490-5 | Purpura
Patient was taking Minipress (View Usage). Patient had the following side effects: purpura on Jan 11, 2007 from JAPAN Additional patient health information: Male patient , 54 years of age, . Minipress dosage: . During the same period patient was treated with EXCEGRAN (View Excegran Review and Excegran Label ), TEGRETOL (View Tegretol Review and Tegretol Label ), ZESTRIL (View Zestril Review and Zestril Label ), URSO (View Urso Review and Urso Label ).

5191663-4 | Cerebrovascular Accident
Adverse event was reported on Dec 07, 2006 by a Male patient taking Minipress (View Usage) (Dosage: ) . Location: UNITED STATES , 74 years of age, After Minipress was administered, patient had the following side effects: cerebrovascular accident. During the same period patient was treated with CLONIDINE (View Clonidine Review and Clonidine Label ).

5191630-0 | Purpura
on Dec 07, 2006 Male patient from JAPAN , 54 years of age, was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: purpura. Minipress dosage: Oral. During the same period patient was treated with ZONISAMIDE (Oral) (View Zonisamide Review and Zonisamide Label ), URSO (USODEOXYCHOLIC ACID) (View Urso (usodeoxycholic Acid) Review and Urso (usodeoxycholic Acid) Label ), TEGRETOL (Oral) (View Tegretol Review and Tegretol Label ), ZESTRIL (Oral) (View Zestril Review and Zestril Label ).

5174447-2 | Purpura
on Nov 28, 2006 Male patient from JAPAN , 54 years of age, was treated with Minipress (View Usage). Patient had the following side effects: purpura. Minipress dosage: Oral. During the same period patient was treated with ZONISAMIDE (Oral) (View Zonisamide Review and Zonisamide Label ), TEGRETOL (Oral) (View Tegretol Review and Tegretol Label ), ZESTRIL (Oral) (View Zestril Review and Zestril Label ), URSO (URSODEOXYCHOLIC ACID) (View Urso (ursodeoxycholic Acid) Review and Urso (ursodeoxycholic Acid) Label ).

5165526-4 | Purpura
Patient was taking Minipress (View Usage). After Minipress was administered, patient had the following side effects: purpura on Nov 09, 2006 from JAPAN Additional patient health information: Male patient , 54 years of age, . Minipress dosage: Oral. During the same period patient was treated with ZONISAMIDE (Oral) (View Zonisamide Review and Zonisamide Label ), TEGRETOL (Oral) (View Tegretol Review and Tegretol Label ), ZESTRIL (Oral) (View Zestril Review and Zestril Label ), URSO (URSODEOXYCHOLIC ACID) (View Urso (ursodeoxycholic Acid) Review and Urso (ursodeoxycholic Acid) Label ).

5114855-9 | Depressed Level Of Consciousness, Orthostatic Hypotension
Adverse event was reported on Sep 11, 2006 by a Male patient taking Minipress (View Usage) (Dosage: 2.5 Mg (2.5 Mg, Once), Oral) was diagnosed with benign prostatic hyperplasia and. Location: INDIA , 78 years of age, Patient experienced the following unwanted or unexpected effects: depressed level of consciousness, orthostatic hypotension. Patient was hospitalized.

5109771-2 | Blood Pressure Increased
on Sep 05, 2006 Male patient from AUSTRALIA , 69 years of age, was diagnosed with hypertension, sleep disorder (What is sleep disorder?) and was treated with Minipress (View Usage). Patient had the following side effects: blood pressure increased. Minipress dosage: 2 Mg (1 Mg, 2 In 1 D), Oral. During the same period patient was treated with HERBAL PREPARATION (HERBAL PREPARATION) (View Herbal Preparation (herbal Preparation) Review and Herbal Preparation (herbal Preparation) Label ), DURIDE (ISOSORBIDE MONONITRATE) (View Duride (isosorbide Mononitrate) Review and Duride (isosorbide Mononitrate) Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), AVAPRO HCT (HYDROCHLOROTHIAZIDE, IRBESARTAN) (View Avapro Hct (hydrochlorothiazide, Irbesartan) Review and Avapro Hct (hydrochlorothiazide, Irbesartan) Label ), RANI 2 (RANITIDINE HYDROCHLORIDE) (View Rani 2 (ranitidine Hydrochloride) Review and Rani 2 (ranitidine Hydrochloride) Label ), VASOCARDOL (DILTIAZEM HYDROCHLORIDE) (View Vasocardol (diltiazem Hydrochloride) Review and Vasocardol (diltiazem Hydrochloride) Label ). Patient was hospitalized.

5108029-5 | Blood Pressure Decreased, Incorrect Dose Administered, Suicide Attempt
on Sep 04, 2006 Male patient from JAPAN , 52 years of age, was treated with Minipress (View Usage). After Minipress was administered, patient had the following side effects: blood pressure decreased, incorrect dose administered, suicide attempt. Minipress dosage: 10 Tablets (0.5 Mg, Once), Oral.

5090878-3 | Depressed Level Of Consciousness, Orthostatic Hypotension
Patient was taking Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: depressed level of consciousness, orthostatic hypotension on Aug 11, 2006 from INDIA Additional patient health information: Male patient , 78 years of age, was diagnosed with benign prostatic hyperplasia and. Minipress dosage: 2.5 Mg (2.5 Mg, Frequency: Once Interval Daily), Oral. Patient was hospitalized.

4911652-1 | Anxiety, Blood Cholesterol Increased, Blood Pressure Increased, Body Height Decreased, Condition Aggravated, Eye Haemorrhage
Adverse event was reported on Feb 02, 2006 by a Female patient taking Minipress (View Usage) (Dosage: 2 Mg (1 Mg, Bid, Interval: Every Day), Oral) was diagnosed with hypertension, blood cholesterol increased and. Location: UNITED STATES , 62 years of age, Patient had the following side effects: anxiety (What is anxiety?), blood cholesterol increased, blood pressure increased, body height decreased, condition aggravated, eye haemorrhage. During the same period patient was treated with PRAZOSIN GITS (6 Mg (2 Mg, Tid Interval: Every Day), Oral) (View Prazosin Gits Review and Prazosin Gits Label ), ZETIA (View Zetia Review and Zetia Label ), ANTIHYPERTENSIVES (ANTIHYPERTENSIVES) (View Antihypertensives (antihypertensives) Review and Antihypertensives (antihypertensives) Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

4898453-8 | Arthralgia, Blood Cholesterol Increased, Blood Pressure Increased, Body Height Decreased, Carpal Tunnel Decompression, Eye Haemorrhage, Oedema Mouth
on Jan 16, 2006 Female patient from UNITED STATES , 62 years of age, was diagnosed with hypertension, blood cholesterol increased and was treated with Minipress (View Usage). After Minipress was administered, patient had the following side effects: arthralgia, blood cholesterol increased, blood pressure increased, body height decreased, carpal tunnel decompression, eye haemorrhage, oedema mouth. Minipress dosage: 2 Mg (1 Mg, Bid Interval: Every Day), Oral. During the same period patient was treated with PRAZOSIN GITS (6 Mg (2 Mg, Tid Interval: Every Day), Oral) (View Prazosin Gits Review and Prazosin Gits Label ), ZETIA (View Zetia Review and Zetia Label ), ANTIHYPERTENSIVES (ANTIHYPERTENSIVES) (View Antihypertensives (antihypertensives) Review and Antihypertensives (antihypertensives) Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

4875352-9 | Arthralgia, Blood Cholesterol Increased, Blood Pressure Increased, Body Height Decreased, Ocular Vascular Disorder, Oedema Mouth
on Dec 28, 2005 Female patient from UNITED STATES , 62 years of age, was diagnosed with hypertension, blood cholesterol increased and was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, blood cholesterol increased, blood pressure increased, body height decreased, ocular vascular disorder, oedema mouth. Minipress dosage: 2 Mg (1 Mg, Bid Interval: Every Day), Oral. During the same period patient was treated with PRAZOSIN GITS (6 Mg (2 Mg, Tid Interval: Every Day), Oral) (View Prazosin Gits Review and Prazosin Gits Label ), ZETIA (View Zetia Review and Zetia Label ), ANTIHYPERTENSIVES (ANTIHYPERTENSIVES) (View Antihypertensives (antihypertensives) Review and Antihypertensives (antihypertensives) Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

4871258-X | Arthralgia, Blood Cholesterol Increased, Body Height Decreased, Cervical Dysplasia, Condition Aggravated, Eye Haemorrhage, Hypertension
Patient was taking Minipress (View Usage). Patient had the following side effects: arthralgia, blood cholesterol increased, body height decreased, cervical dysplasia, condition aggravated, eye haemorrhage, hypertension on Dec 16, 2005 from UNITED STATES Additional patient health information: Female patient , 62 years of age, was diagnosed with hypertension, blood cholesterol increased and. Minipress dosage: 2 Mg (1 Mg, Bid Interval: Every Day) , Oral. During the same period patient was treated with PRAZOSIN GITS (6 Mg (2 Mg, Tid Interval: Every Day), Oral) (View Prazosin Gits Review and Prazosin Gits Label ), ZETIA (View Zetia Review and Zetia Label ), ANTIHYPERTENSIVES (ANTIHYPERTENSIVES) (View Antihypertensives (antihypertensives) Review and Antihypertensives (antihypertensives) Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

4860927-3 | Acute Respiratory Failure, Interstitial Lung Disease, Lymphadenopathy, Metastatic Neoplasm
Adverse event was reported on Dec 05, 2005 by a Male patient taking Minipress (View Usage) (Dosage: Oral) was diagnosed with ill-defined disorder, headache (What is headache?) and. Location: JAPAN , 72 years of age, After Minipress was administered, patient had the following side effects: acute respiratory failure, interstitial lung disease, lymphadenopathy, metastatic neoplasm. During the same period patient was treated with LOXONIN (LOXOPROFEN SODIUM) (View Loxonin (loxoprofen Sodium) Review and Loxonin (loxoprofen Sodium) Label ), MARZULENE S (LEVOFLUTAMIDE, SODIUM GUALENATE) (Oral) (View Marzulene S (levoflutamide, Sodium Gualenate) Review and Marzulene S (levoflutamide, Sodium Gualenate) Label ), JUVELA (TOCOPHEROL) (View Juvela (tocopherol) Review and Juvela (tocopherol) Label ), COMELIAN (DILAZEP DIHYDROCHLORIDE) (Oral) (View Comelian (dilazep Dihydrochloride) Review and Comelian (dilazep Dihydrochloride) Label ), CALSLOT (MANIDIPINE HYDROCHLORIDE) (Oral) (View Calslot (manidipine Hydrochloride) Review and Calslot (manidipine Hydrochloride) Label ), THEO DUR (View Theo-dur Review and Theo-dur Label ), ASTOMIN (DIMEMORFAN PHOSPHATE) (Oral) (View Astomin (dimemorfan Phosphate) Review and Astomin (dimemorfan Phosphate) Label ), BISOLVON (BROMHEXINE HYDROCHLORIDE) (View Bisolvon (bromhexine Hydrochloride) Review and Bisolvon (bromhexine Hydrochloride) Label ). Patient was hospitalized.

4805664-6 | Dementia Alzheimer's Type
on Oct 08, 2005 Male patient from UNITED STATES , 76 years of age, was diagnosed with ill-defined disorder and was treated with Minipress (View Usage). Patient experienced the following unwanted or unexpected effects: dementia alzheimer's type. Minipress dosage: . Patient was hospitalized.

4577502-0 | Anorectal Disorder, Surgical Procedure Repeated, Thrombosis
on Jan 26, 2005 Male patient from , 67 years of age, weighting 176.4 lb, was diagnosed with hypertension and was treated with Minipress (View Usage). Patient had the following side effects: anorectal disorder, surgical procedure repeated, thrombosis. Minipress dosage: 1 Mg (1 Mg, 1 In 1 D), Oral. During the same period patient was treated with DYAZIDE (View Dyazide Review and Dyazide Label ), CLONIDINE (View Clonidine Review and Clonidine Label ).