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perscribed metformin 1000mg twice daily diabetes 2,lysinopril hypertension&highbloodpressure, simvastatin20mg,dyazide,...Keep Reading

Dyazide caused muscle weakness to the point that it interferred with my recovery from ...Keep Reading

In 2007 and 2008 a dermatologist at the U. of Arizona Cancer Center ...Keep Reading

Was on Dyazide for fluid retention. Was given Arthrotec for back pain ...Keep Reading

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Death (1)
Muscle Spasms (1)
Purpura (1)
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Common Dyazide Side Effects

top 5 Dyazide|Death|Muscle spa|Purpura adverse effects>>See All Dyazide Side Effects

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Dyazide adverse events reported to FDA.

Have You Experienced unusual Dyazide symptoms? PatientsVille.com collects and analyzes Dyazide side effect and adverse reports submitted by Dyazide users, such as high blood pressure (198/100), severe constipation, fatigue|.

Summary

FDA Adverse Reports: 120. View All

Dyazide FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 26

Dyazide Dosage, Warnings, Usage.

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Most Reported
1Muscle Spasms
2Purpura
3Death
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Recent Drug Reports

high blood pressure (198/100), severe constipation, fatigue

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

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6870689-6 | Ill-defined Disorder
on Mar 22, 2010 Female patient from UNITED STATES , 51 years of age, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: ill-defined disorder. Dyazide dosage: .

6870685-9 | Product Quality Issue
Patient was taking Dyazide (View Usage). Patient had the following side effects: product quality issue on Feb 03, 2010 from UNITED STATES Additional patient health information: Female patient , 66 years of age, . Dyazide dosage: 1loz Per Day.

6870684-7 | Dry Eye
Adverse event was reported on Nov 12, 2009 by a Female patient taking Dyazide (View Usage) (Dosage: ) . Location: UNITED STATES , 97 years of age, After Dyazide was administered, patient had the following side effects: dry eye.

6870682-3 | Pruritus, Rash, Urticaria, Weight Decreased
on Oct 12, 2009 Female patient from UNITED STATES , 80 years of age, was diagnosed with hypertension and was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, rash (What is rash?), urticaria, weight decreased. Dyazide dosage: 1cap Per Day. During the same period patient was treated with COREG CR (View Coreg Cr Review and Coreg Cr Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ).


6701197-0 | Cystitis, Nausea, Product Substitution Issue
on Apr 28, 2010 Female patient from UNITED STATES , weighting 145.0 lb, was diagnosed with hypertension and was treated with Dyazide (View Usage). Patient had the following side effects: cystitis, nausea (What is nausea?), product substitution issue. Dyazide dosage: .

6647282-3 | Idiopathic Thrombocytopenic Purpura, Malaise
Patient was taking Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: idiopathic thrombocytopenic purpura, malaise on Mar 15, 2010 from UNITED STATES Additional patient health information: Female patient , 68 years of age, . Dyazide dosage: .

6629640-6 | Blood Sodium Decreased, Fall, Heart Rate Decreased, Malaise, Syncope
Adverse event was reported on Mar 10, 2010 by a Female patient taking Dyazide (View Usage) (Dosage: 1 Daily Oral) was diagnosed with premenstrual syndrome (What is premenstrual syndrome?) and. Location: UNITED STATES , 48 years of age, weighting 170.0 lb, Patient experienced the following unwanted or unexpected effects: blood sodium decreased, fall (What is fall?), heart rate decreased, malaise, syncope. During the same period patient was treated with TRILEPTAL (View Trileptal Review and Trileptal Label ), PROZAC (View Prozac Review and Prozac Label ), XANAX (View Xanax Review and Xanax Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ).

6388701-X | Atrial Fibrillation, Dyspnoea, Hypokalaemia
on Oct 02, 2009 Female patient from UNITED STATES , weighting 152.0 lb, was diagnosed with oedema and was treated with Dyazide (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), dyspnoea, hypokalaemia. Dyazide dosage: 37.5/25 Oneqd Po.

6285931-2 | Erythema, Hypersensitivity, Insomnia
on Apr 20, 2009 Male patient from UNITED STATES , 54 years of age, was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: erythema, hypersensitivity, insomnia. Dyazide dosage: .

6285926-9 | Dizziness
Patient was taking Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?) on Jan 27, 2009 from UNITED STATES Additional patient health information: Female patient , 81 years of age, was diagnosed with hypertension, psoriasis, osteoporosis (What is osteoporosis?) and. Dyazide dosage: 25mg Per Day. During the same period patient was treated with HUMIRA (40ml Every Two Weeks) (View Humira Review and Humira Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), ACETYLSALICYLIC ACID (81mg Per Day) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), CALCIUM (View Calcium Review and Calcium Label ).

6285925-7 | Dysgeusia, Glossodynia
Adverse event was reported on Dec 15, 2008 by a Male patient taking Dyazide (View Usage) (Dosage: ) was diagnosed with meniere's disease (What is meniere's disease?) and. Location: UNITED STATES , 58 years of age, Patient had the following side effects: dysgeusia, glossodynia. During the same period patient was treated with MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), PREVACID (View Prevacid Review and Prevacid Label ).

6285924-5 | Blood Pressure Increased, Headache, Malaise, Oropharyngeal Pain
on Nov 14, 2008 Female patient from UNITED STATES , 72 years of age, was diagnosed with hypertension and was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: blood pressure increased, headache (What is headache?), malaise, oropharyngeal pain. Dyazide dosage: 37.5mg Variable Dose. During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ).

6285923-3 | Hypertension
on Oct 02, 2008 Female patient from UNITED STATES , 61 years of age, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension. Dyazide dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ).

6285922-1 | Pruritus
Patient was taking Dyazide (View Usage). Patient had the following side effects: pruritus on Aug 12, 2008 from UNITED STATES Additional patient health information: Female patient , 58 years of age, . Dyazide dosage: .

6285921-X | Oedema Peripheral
Adverse event was reported on Aug 12, 2008 by a Female patient taking Dyazide (View Usage) (Dosage: 1cap Per Day) was diagnosed with hypertension and. Location: UNITED STATES , 64 years of age, After Dyazide was administered, patient had the following side effects: oedema peripheral. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ).

6285919-1 | Dysgeusia, Product Quality Issue
on Jul 29, 2008 Female patient from UNITED STATES , 70 years of age, weighting 162.3 lb, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: dysgeusia, product quality issue. Dyazide dosage: . During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), PREVACID (View Prevacid Review and Prevacid Label ), OGEN (View Ogen Review and Ogen Label ).

6194990-7 | Neoplasm Malignant
on May 11, 2009 Female patient from UNITED STATES , 59 years of age, was treated with Dyazide (View Usage). Patient had the following side effects: neoplasm malignant. Dyazide dosage: .

6186901-5 | Chills, Feeling Cold
Patient was taking Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: chills, feeling cold on May 08, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 130.7 lb, . Dyazide dosage: 1 Capsule Qd Oral. During the same period patient was treated with ACTONEL (View Actonel Review and Actonel Label ), ALEVE (View Aleve Review and Aleve Label ), HYDROXYCHLOROQUINE SULFATE (View Hydroxychloroquine Sulfate Review and Hydroxychloroquine Sulfate Label ).

6168475-8 |
Adverse event was reported on Apr 21, 2009 by a Female patient taking Dyazide (View Usage) (Dosage: ) . Location: UNITED STATES , 59 years of age, .

6092360-3 | Hypercalcaemia
on Feb 23, 2009 Male patient from UNITED STATES , weighting 186.4 lb, was treated with Dyazide (View Usage). Patient had the following side effects: hypercalcaemia. Dyazide dosage: 1 Capsule Qd Oral. During the same period patient was treated with AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), DIPHENHYDRAMINE ORAL (View Diphenhydramine Oral Review and Diphenhydramine Oral Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), MVI (MULTIVITAMINS) (View Mvi (multivitamins) Review and Mvi (multivitamins) Label ), PERCOCET 5 MG/35 MG (OXYCODONE 5 MG/ ACETAMINOPHEN 325) (View Percocet 5 Mg/35 Mg (oxycodone 5 Mg/ Acetaminophen 325) Review and Percocet 5 Mg/35 Mg (oxycodone 5 Mg/ Acetaminophen 325) Label ).

6029953-5 | Blood Amylase Decreased, Blood Calcium Decreased, Blood Magnesium Decreased, Blood Phosphorus Decreased, Blood Potassium Decreased, Blood Sodium Decreased, Blood Urea Decreased, Brain Natriuretic Peptide Increased, Cardiac Failure Congestive
on Jan 05, 2009 Female patient from UNITED STATES , 61 years of age, was diagnosed with restless legs syndrome and was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: blood amylase decreased, blood calcium decreased, blood magnesium decreased, blood phosphorus decreased, blood potassium decreased, blood sodium decreased, blood urea decreased, brain natriuretic peptide increased, cardiac failure congestive. Dyazide dosage: 1cap Per Day. During the same period patient was treated with LYRICA (50mg Per Day) (View Lyrica Review and Lyrica Label ), QUININE (View Quinine Review and Quinine Label ), ZEGERID (View Zegerid Review and Zegerid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), COLACE (View Colace Review and Colace Label ), PREMARIN (View Premarin Review and Premarin Label ), DILTIAZEM (View Diltiazem Review and Diltiazem Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ). Patient was hospitalized.

5931510-3 | Cholelithiasis, Pancreatitis
Patient was taking Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: cholelithiasis, pancreatitis on Oct 21, 2008 from UNITED STATES Additional patient health information: Female patient , 60 years of age, . Dyazide dosage: .

5836834-6 | Blood Amylase Decreased, Blood Calcium Decreased, Blood Magnesium Decreased, Blood Phosphorus Decreased, Blood Potassium Decreased, Blood Sodium Decreased, Blood Urea Decreased, Brain Natriuretic Peptide Increased, Cardiac Failure Congestive
Adverse event was reported on Jul 31, 2008 by a Female patient taking Dyazide (View Usage) (Dosage: 1cap Per Day) was diagnosed with restless legs syndrome and. Location: UNITED STATES , 61 years of age, Patient had the following side effects: blood amylase decreased, blood calcium decreased, blood magnesium decreased, blood phosphorus decreased, blood potassium decreased, blood sodium decreased, blood urea decreased, brain natriuretic peptide increased, cardiac failure congestive. During the same period patient was treated with LYRICA (50mg Per Day) (View Lyrica Review and Lyrica Label ), QUININE (View Quinine Review and Quinine Label ), ZEGERID (View Zegerid Review and Zegerid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), COLACE (View Colace Review and Colace Label ), PREMARIN (View Premarin Review and Premarin Label ), DILTIAZEM HCL (View Diltiazem Hcl Review and Diltiazem Hcl Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ). Patient was hospitalized.

5826734-X | Diabetes Mellitus
on Jul 28, 2008 Male patient from UNITED STATES , 44 years of age, weighting 396.0 lb, was diagnosed with myocardial infarction and was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: diabetes mellitus. Dyazide dosage: 1 Day Po.

5823239-7 | Dyspnoea, Fatigue
on May 27, 2008 Female patient from UNITED STATES , 41 years of age, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, fatigue. Dyazide dosage: . During the same period patient was treated with NEBIVOLOL HCL (View Nebivolol Hcl Review and Nebivolol Hcl Label ).

5823238-5 | Nausea
Patient was taking Dyazide (View Usage). Patient had the following side effects: nausea (What is nausea?) on May 06, 2008 from UNITED STATES Additional patient health information: Female patient , 78 years of age, was diagnosed with hypertension and. Dyazide dosage: 37.5mg Per Day. During the same period patient was treated with VITAMIN E (View Vitamin E Review and Vitamin E Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), SINGULAIR (View Singulair Review and Singulair Label ), ALLEGRA (View Allegra Review and Allegra Label ), PRILOSEC (View Prilosec Review and Prilosec Label ).

5823236-1 | Arrhythmia, Cough
Adverse event was reported on Feb 29, 2008 by a Female patient taking Dyazide (View Usage) (Dosage: ) . Location: UNITED STATES , 80 years of age, After Dyazide was administered, patient had the following side effects: arrhythmia (What is arrhythmia?), cough. During the same period patient was treated with AVAPRO (View Avapro Review and Avapro Label ).

5823235-X | Dizziness
on Mar 10, 2008 Male patient from UNITED STATES , 66 years of age, was diagnosed with hypertension and was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?). Dyazide dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5823234-8 | Hair Growth Abnormal
on Jan 22, 2008 Female patient from UNITED STATES , 74 years of age, was diagnosed with hypertension and was treated with Dyazide (View Usage). Patient had the following side effects: hair growth abnormal. Dyazide dosage: 37.5mg Per Day. During the same period patient was treated with VERAPAMIL (View Verapamil Review and Verapamil Label ), ACTONEL (View Actonel Review and Actonel Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), COUMADIN (View Coumadin Review and Coumadin Label ).

5823233-6 | Arrhythmia, Arterial Occlusive Disease, Arteriosclerosis, Dizziness, Ill-defined Disorder, Venous Pressure
Patient was taking Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: arrhythmia (What is arrhythmia?), arterial occlusive disease, arteriosclerosis, dizziness (What is dizziness?), ill-defined disorder, venous pressure on Feb 11, 2008 from UNITED STATES Additional patient health information: Female patient , 49 years of age, . Dyazide dosage: .

5823231-2 | Anorexia, Asthenia, Dizziness, Dry Mouth, Dyspepsia
Adverse event was reported on Oct 01, 2007 by a Female patient taking Dyazide (View Usage) (Dosage: 1tab Per Day) was diagnosed with hypertension and. Location: UNITED STATES , 49 years of age, Patient experienced the following unwanted or unexpected effects: anorexia, asthenia, dizziness (What is dizziness?), dry mouth, dyspepsia.

5823230-0 | Pruritus, Rash
on Sep 04, 2007 Female patient from UNITED STATES , 78 years of age, was diagnosed with hypertension and was treated with Dyazide (View Usage). Patient had the following side effects: pruritus, rash (What is rash?). Dyazide dosage: 25mg Per Day. During the same period patient was treated with ZANTAC (150mg As Required) (View Zantac Review and Zantac Label ), XANAX (View Xanax Review and Xanax Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ARIMIDEX (View Arimidex Review and Arimidex Label ), COMBIVENT (View Combivent Review and Combivent Label ), CELEXA (View Celexa Review and Celexa Label ), CALCIUM D (View Calcium D Review and Calcium D Label ).

5823228-2 | Blood Pressure Increased, Headache, Nausea
on Aug 21, 2007 Female patient from UNITED STATES , 42 years of age, was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: blood pressure increased, headache (What is headache?), nausea (What is nausea?). Dyazide dosage: .

5823227-0 | Chest Pain, Dry Mouth, Dyspnoea
Patient was taking Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dry mouth, dyspnoea on Jul 27, 2007 from UNITED STATES Additional patient health information: Female patient , 49 years of age, was diagnosed with hypertension and. Dyazide dosage: 37.5mg Per Day. During the same period patient was treated with ALBUTEROL (View Albuterol Review and Albuterol Label ), MUSCLE RELAXER (View Muscle Relaxer Review and Muscle Relaxer Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

5688996-1 | Erythema, Joint Swelling, Oedema Peripheral
Adverse event was reported on Mar 25, 2008 by a Female patient taking Dyazide (View Usage) (Dosage: 1cap Per Day) was diagnosed with hypertension and. Location: UNITED STATES , 47 years of age, Patient had the following side effects: erythema, joint swelling, oedema peripheral. During the same period patient was treated with PHENTERMINE (View Phentermine Review and Phentermine Label ), MULTIPLE VITAMIN (View Multiple Vitamin Review and Multiple Vitamin Label ). Patient was hospitalized.

5669891-0 | Cystitis, Nausea
on Mar 14, 2008 Female patient from UNITED STATES , weighting 164.0 lb, was diagnosed with hypertension and was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: cystitis, nausea (What is nausea?). Dyazide dosage: 37.5/25 Mg Daily.

5512836-4 | Dry Skin
on Nov 08, 2007 Male patient from UNITED STATES , 70 years of age, weighting 187.6 lb, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: dry skin. Dyazide dosage: .

5512614-6 | Renal Impairment
Patient was taking Dyazide (View Usage). Patient had the following side effects: renal impairment on Nov 08, 2007 from UNITED STATES Additional patient health information: Male patient , 63 years of age, weighting 254.4 lb, . Dyazide dosage: .

5404811-5 | Diverticular Perforation
Adverse event was reported on Jul 31, 2007 by a Female patient taking Dyazide (View Usage) (Dosage: Unk, Unk) was diagnosed with hypertension and. Location: UNITED STATES , 84 years of age, After Dyazide was administered, patient had the following side effects: diverticular perforation. During the same period patient was treated with DIOVAN (320 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized.

5401505-7 | Gallbladder Disorder
on Apr 30, 2007 Female patient from UNITED STATES , 89 years of age, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: gallbladder disorder. Dyazide dosage: .

5401504-5 | Burning Sensation, Middle Insomnia, Nausea, Night Sweats
on Mar 27, 2007 Female patient from UNITED STATES , 84 years of age, was treated with Dyazide (View Usage). Patient had the following side effects: burning sensation, middle insomnia, nausea (What is nausea?), night sweats. Dyazide dosage: 1cap Per Day. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ).

5401501-X | Cystitis Noninfective
Patient was taking Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: cystitis noninfective on Mar 08, 2007 from UNITED STATES Additional patient health information: Female patient , 84 years of age, was diagnosed with hypertension and. Dyazide dosage: 1cap Per Day. During the same period patient was treated with TENORMIN (100mg Per Day) (View Tenormin Review and Tenormin Label ), NORVASC (2.5mg Per Day) (View Norvasc Review and Norvasc Label ), NEXIUM (10mg Per Day) (View Nexium Review and Nexium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (20mg Per Day) (View Lipitor Review and Lipitor Label ).

5401500-8 | Balance Disorder, Constipation, Dizziness
Adverse event was reported on Mar 02, 2007 by a Female patient taking Dyazide (View Usage) (Dosage: 10mg Per Day) was diagnosed with hypertension, depression (What is depression?) and. Location: UNITED STATES , 90 years of age, Patient experienced the following unwanted or unexpected effects: balance disorder, constipation (What is constipation?), dizziness (What is dizziness?). During the same period patient was treated with PAXIL (10mg Per Day) (View Paxil Review and Paxil Label ), LIPITOR (View Lipitor Review and Lipitor Label ), XALATAN (View Xalatan Review and Xalatan Label ).

5401499-4 | Blister, Fall
on Mar 01, 2007 Female patient from UNITED STATES , 53 years of age, was treated with Dyazide (View Usage). Patient had the following side effects: blister, fall (What is fall?). Dyazide dosage: . During the same period patient was treated with MAXZIDE (View Maxzide Review and Maxzide Label ).

5401497-0 | Lichen Planus
on Jan 23, 2007 Female patient from UNITED STATES , 87 years of age, was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: lichen planus. Dyazide dosage: .

5401496-9 | Muscle Spasms
Patient was taking Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: muscle spasms on Jan 09, 2007 from UNITED STATES Additional patient health information: Female patient , 68 years of age, . Dyazide dosage: .

5401495-7 | Fatigue, Increased Appetite, Somnolence
Adverse event was reported on Dec 04, 2006 by a Female patient taking Dyazide (View Usage) (Dosage: ) was diagnosed with urine calcium increased and. Location: UNITED STATES , 42 years of age, Patient had the following side effects: fatigue, increased appetite, somnolence.

5401488-X | Blood Pressure Fluctuation
on Aug 29, 2006 Female patient from UNITED STATES , 65 years of age, was diagnosed with meniere's disease (What is meniere's disease?) and was treated with Dyazide (View Usage). After Dyazide was administered, patient had the following side effects: blood pressure fluctuation. Dyazide dosage: .

5401486-6 | Alopecia
on Aug 21, 2006 Female patient from UNITED STATES , 64 years of age, was treated with Dyazide (View Usage). Patient experienced the following unwanted or unexpected effects: alopecia. Dyazide dosage: 25mg Per Day. During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), LIPITOR (View Lipitor Review and Lipitor Label ).

5401485-4 | Oedema Peripheral
Patient was taking Dyazide (View Usage). Patient had the following side effects: oedema peripheral on Aug 17, 2006 from UNITED STATES Additional patient health information: Male patient , 62 years of age, was diagnosed with hypertension and. Dyazide dosage: 1cap Per Day. During the same period patient was treated with NADOL (View Nadol Review and Nadol Label ), PREVACID (View Prevacid Review and Prevacid Label ).

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Dyazide Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

laura granberry   Location unknown

2:07am on Wednesday, October 8th, 2008

i take triamt/hctz37.5(dyazide) furosemide20mg;(lasix ) potassium,nexium,I have zip lock sandwich ba... read more »

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 Dyazide 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 Dyazide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Dyazide 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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About Dyazide : Risks and Benefits, News and Updates, Dyazide video and TV resources

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Dyazide Reactions
Abdominal Pain Upper
Activities Of Daily Living Impaired
Alopecia
Asthenia
Atrial FibrillationWhat is Atrial fibrillation?
Balance Disorder
Blood Magnesium Decreased
Blood Potassium Decreased
Blood Pressure Increased
Blood Sodium Decreased
Chest PainWhat is Chest pain?
Chills
Condition Aggravated
Cough
Diabetes Mellitus
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
HeadacheWhat is Headache?
Hyperkalaemia
Hypoaesthesia
Ill-defined Disorder
Muscle Spasms
NauseaWhat is Nausea?
Oedema Peripheral
Pruritus
RashWhat is Rash?
Visual Disturbance
Vomiting
Dyazide 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 Dyazide 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!