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Zestoretic adverse events reported to FDA.

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Summary

FDA Adverse Reports: 78. View All

Zestoretic FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 32

Zestoretic Dosage, Warnings, Usage.

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

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7013570-4 | Angioedema, Cervix Erythema, Tongue Oedema
on Sep 13, 2010 Male patient from FRANCE , 77 years of age, was diagnosed with hypertension and was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, cervix erythema, tongue oedema. Zestoretic dosage: . During the same period patient was treated with COVERAM (View Coveram Review and Coveram Label ), TRIATEC (View Triatec Review and Triatec Label ). Patient was hospitalized.

6941301-2 | Cough
Patient was taking Zestoretic (View Usage). Patient had the following side effects: cough on Aug 24, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 228.0 lb, was diagnosed with hypertension and. Zestoretic dosage: .

6933638-8 | Acute Myocardial Infarction
Adverse event was reported on Aug 13, 2010 by a Female patient taking Zestoretic (View Usage) (Dosage: 20+12.5 Mg/day) . Location: ITALY , 89 years of age, After Zestoretic was administered, patient had the following side effects: acute myocardial infarction. During the same period patient was treated with TICLID (View Ticlid Review and Ticlid Label ). Patient was hospitalized.

6910368-X | Toxic Skin Eruption
on Jul 28, 2010 Male patient from FRANCE , 69 years of age, weighting 138.9 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: toxic skin eruption. Zestoretic dosage: 20+12.5 Mg/day. During the same period patient was treated with AMLOR (View Amlor Review and Amlor Label ). Patient was hospitalized.


6906059-1 | Toxic Skin Eruption
on Jul 28, 2010 Male patient from FRANCE , 69 years of age, weighting 138.9 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). Patient had the following side effects: toxic skin eruption. Zestoretic dosage: 125/25 Mg/day. During the same period patient was treated with AMLOR (View Amlor Review and Amlor Label ). Patient was hospitalized.

6879823-5 | Hyperkalaemia, Hypotension, Shock
Patient was taking Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: hyperkalaemia, hypotension, shock on Jul 20, 2010 from ITALY Additional patient health information: Female patient , 65 years of age, was diagnosed with hypertension and. Zestoretic dosage: 20+12.5 Mg Daily. During the same period patient was treated with ISOPTIN (View Isoptin Review and Isoptin Label ), TIMOPTOL (View Timoptol Review and Timoptol Label ). Patient was hospitalized.

6862008-6 | Cough
Adverse event was reported on Jul 20, 2010 by a Male patient taking Zestoretic (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 299.0 lb, Patient experienced the following unwanted or unexpected effects: cough.

6831902-4 | Polyp
on Jul 01, 2010 Male patient from UNITED STATES , 52 years of age, weighting 240.1 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Zestoretic (View Usage). Patient had the following side effects: polyp. Zestoretic dosage: . During the same period patient was treated with REMICADE (View Remicade Review and Remicade Label ), CHOLESTYRAMINE (View Cholestyramine Review and Cholestyramine Label ), SULFASALAZINE (View Sulfasalazine Review and Sulfasalazine Label ), NASACORT AQ (View Nasacort Aq Review and Nasacort Aq Label ).

6830624-3 | Cough
on Jul 09, 2010 Female patient from UNITED STATES , weighting 133.0 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: cough. Zestoretic dosage: 20 - 12.5 Mg Daily Oral.

6802675-6 | Angioedema, Antinuclear Antibody Positive, Arthralgia, Photosensitivity Reaction, Pyrexia
Patient was taking Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, antinuclear antibody positive, arthralgia, photosensitivity reaction, pyrexia on Jun 17, 2010 from FRANCE Additional patient health information: Male patient , 60 years of age, was diagnosed with hypertension and. Zestoretic dosage: . During the same period patient was treated with AMLOR (View Amlor Review and Amlor Label ).

6785816-9 | Hypoaesthesia Facial
Adverse event was reported on Jun 21, 2010 by a Female patient taking Zestoretic (View Usage) (Dosage: 10/12.5 Mg Daily P.o.) was diagnosed with hypertension and. Location: UNITED STATES , weighting 196.0 lb, Patient had the following side effects: hypoaesthesia facial.

6781573-0 | Renal Failure Acute
on Jun 16, 2010 Male patient from FRANCE , 97 years of age, was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: renal failure acute. Zestoretic dosage: 20/12.5 Mg Daily. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), VOLTAREN (View Voltaren Review and Voltaren Label ).

6770507-0 | Renal Failure Acute
on Jun 10, 2010 Male patient from FRANCE , 97 years of age, was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute. Zestoretic dosage: 20/12.5 Mg Daily. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), VOLTAREN (View Voltaren Review and Voltaren Label ).

6721481-4 | Bladder Cancer, Deafness, Eye Disorder, Eye Haemorrhage, Headache, Heart Rate Irregular, Hypertension, Nervous System Disorder, Pain
Patient was taking Zestoretic (View Usage). Patient had the following side effects: bladder cancer (What is bladder cancer?), deafness, eye disorder, eye haemorrhage, headache (What is headache?), heart rate irregular, hypertension, nervous system disorder, pain (What is pain?) on Apr 29, 2010 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 136.9 lb, was diagnosed with hypertension and. Zestoretic dosage: 10-12.5 Mg. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), SULFA (View Sulfa Review and Sulfa Label ), ATENOLOL/CHLORTHIADONE(MYLAN) (View Atenolol/chlorthiadone(mylan) Review and Atenolol/chlorthiadone(mylan) Label ), BACTRIM (View Bactrim Review and Bactrim Label ).

6686261-7 | Dizziness, Headache, Hypotension
Adverse event was reported on Apr 12, 2010 by a Female patient taking Zestoretic (View Usage) (Dosage: 20+12.5 Mg; 1 Df Daily) was diagnosed with hypertension and. Location: FRANCE , 71 years of age, After Zestoretic was administered, patient had the following side effects: dizziness (What is dizziness?), headache (What is headache?), hypotension. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), LECTIL (View Lectil Review and Lectil Label ), TEGRETOL (View Tegretol Review and Tegretol Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ), LEXOMIL (View Lexomil Review and Lexomil Label ). Patient was hospitalized.

6681435-3 | Hypertension
on Nov 16, 2009 Female patient from UNITED STATES , 45 years of age, was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension. Zestoretic dosage: .

6681432-8 | Abnormal Dreams, Alopecia, Asthenia, Blood Cholesterol Increased, Blood Potassium Increased, Choking, Decreased Appetite, Diarrhoea, Dizziness
on Apr 17, 2009 Female patient from UNITED STATES , 89 years of age, was treated with Zestoretic (View Usage). Patient had the following side effects: abnormal dreams, alopecia, asthenia, blood cholesterol increased, blood potassium increased, choking (What is choking?), decreased appetite, diarrhoea, dizziness (What is dizziness?). Zestoretic dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), AVANDAMET (View Avandamet Review and Avandamet Label ), ATENOL (View Atenol Review and Atenol Label ), NEXIUM (View Nexium Review and Nexium Label ), NORVASC (View Norvasc Review and Norvasc Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), GLUCOTROL (View Glucotrol Review and Glucotrol Label ), DETROL (View Detrol Review and Detrol Label ).

6681430-4 | Hypertension
Patient was taking Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: hypertension on Nov 16, 2009 from UNITED STATES Additional patient health information: Female patient , 41 years of age, . Zestoretic dosage: .

6681429-8 | Hypertension
Adverse event was reported on Nov 16, 2009 by a Male patient taking Zestoretic (View Usage) (Dosage: ) . Location: UNITED STATES , 45 years of age, Patient experienced the following unwanted or unexpected effects: hypertension.

6681427-4 | Hypertension
on Nov 17, 2009 Female patient from UNITED STATES , 51 years of age, was treated with Zestoretic (View Usage). Patient had the following side effects: hypertension. Zestoretic dosage: .

6681416-X | Hypertension
on Nov 16, 2009 Male patient from UNITED STATES , 43 years of age, was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: hypertension. Zestoretic dosage: .

6681415-8 | Hypertension
Patient was taking Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension on Nov 13, 2009 from UNITED STATES Additional patient health information: Male patient , 52 years of age, . Zestoretic dosage: .

6645437-5 | Angioedema, Coma
Adverse event was reported on Mar 18, 2010 by a Female patient taking Zestoretic (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: BELGIUM , 74 years of age, Patient had the following side effects: angioedema, coma. During the same period patient was treated with BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ).

6634093-8 | Fall, Laziness, Somnolence, Upper Limb Fracture
on Mar 05, 2010 Female patient from BRAZIL , 70 years of age, was diagnosed with hypertension and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: fall (What is fall?), laziness, somnolence, upper limb fracture. Zestoretic dosage: . During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ). Patient was hospitalized.

6622777-7 | Deafness, Eye Haemorrhage, Headache, Heart Rate Irregular, Nervous System Disorder, Pain, Renal Failure, Tinnitus, Transient Ischaemic Attack
on Mar 01, 2010 Female patient from UNITED STATES , 70 years of age, weighting 136.9 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: deafness, eye haemorrhage, headache (What is headache?), heart rate irregular, nervous system disorder, pain (What is pain?), renal failure, tinnitus (What is tinnitus?), transient ischaemic attack. Zestoretic dosage: 10-12.5 Mg. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), SULFA (View Sulfa Review and Sulfa Label ), ATENOLOL/CHLORTHIADONE(MYLAN) (View Atenolol/chlorthiadone(mylan) Review and Atenolol/chlorthiadone(mylan) Label ), BACTRIM (View Bactrim Review and Bactrim Label ).

6584479-5 | Cough
Patient was taking Zestoretic (View Usage). Patient had the following side effects: cough on Feb 13, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 182.5 lb, was diagnosed with hypertension and. Zestoretic dosage: 10/12.5mg Daily Oral.

6569626-3 | Blood Pressure Inadequately Controlled
Adverse event was reported on Feb 03, 2010 by a Male patient taking Zestoretic (View Usage) (Dosage: 10/25 Mg Once Daily By Mouth) . Location: UNITED STATES , weighting 181.5 lb, After Zestoretic was administered, patient had the following side effects: blood pressure inadequately controlled.

6500208-5 | Interstitial Lung Disease
on Dec 09, 2009 Male patient from FRANCE , 85 years of age, was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Zestoretic 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 ).

6441555-5 | Interstitial Lung Disease
on Nov 05, 2009 Male patient from FRANCE , 85 years of age, was treated with Zestoretic (View Usage). Patient had the following side effects: interstitial lung disease. Zestoretic dosage: . During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), FELDENE (View Feldene Review and Feldene Label ), LASILIX (View Lasilix Review and Lasilix Label ).

6439297-5 | Deafness, Eye Haemorrhage, Headache, Heart Rate Irregular, Nervous System Disorder, Pain, Renal Failure, Tinnitus, Transient Ischaemic Attack
Patient was taking Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: deafness, eye haemorrhage, headache (What is headache?), heart rate irregular, nervous system disorder, pain (What is pain?), renal failure, tinnitus (What is tinnitus?), transient ischaemic attack on Nov 04, 2009 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 136.9 lb, was diagnosed with hypertension and. Zestoretic dosage: 10/25 Mg. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), SULFA (View Sulfa Review and Sulfa Label ), ATENOLOL/CHLORTHIADONE(MYLAN) (View Atenolol/chlorthiadone(mylan) Review and Atenolol/chlorthiadone(mylan) Label ), BACTRIM (View Bactrim Review and Bactrim Label ).

6371738-4 | Cough, Dizziness, Headache, Nausea
Adverse event was reported on Sep 18, 2009 by a Female patient taking Zestoretic (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 150.0 lb, Patient experienced the following unwanted or unexpected effects: cough, dizziness (What is dizziness?), headache (What is headache?), nausea (What is nausea?).

6268373-5 | Angioedema, Blood Pressure Increased
on Jul 13, 2009 Female patient from UNITED STATES , 43 years of age, was diagnosed with hypertension and was treated with Zestoretic (View Usage). Patient had the following side effects: angioedema, blood pressure increased. Zestoretic dosage: Not Reported Daily Po. During the same period patient was treated with HYDROCHLOROTHIAZIDE (Not Reported Daily Po) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

6152228-0 | Dehydration, Hypotension, Sinus Tachycardia, Syncope
on Dec 17, 2008 Female patient from UNITED STATES , 52 years of age, weighting 202.8 lb, was diagnosed with hypertension, breast cancer (What is breast cancer?) and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: dehydration, hypotension, sinus tachycardia, syncope. Zestoretic dosage: 40/25 Mg. During the same period patient was treated with PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ), BEVACIZUMAB (View Bevacizumab Review and Bevacizumab Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), KYTRIL (View Kytril Review and Kytril Label ), DECADRON (View Decadron Review and Decadron Label ). Patient was hospitalized.

6152227-9 | Dry Throat, Gastrooesophageal Reflux Disease, Increased Upper Airway Secretion, Pharyngeal Oedema
Patient was taking Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: dry throat, gastrooesophageal reflux disease, increased upper airway secretion, pharyngeal oedema on Nov 11, 2008 from UNITED STATES Additional patient health information: Male patient , 58 years of age, weighting 248.0 lb, was diagnosed with hypertension and. Zestoretic dosage: 20/25. During the same period patient was treated with LAMISIL (View Lamisil Review and Lamisil Label ), NIASPAN (View Niaspan Review and Niaspan Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), B VITAMIN (View B Vitamin Review and B Vitamin Label ).

6152226-7 | Arthralgia
Adverse event was reported on Nov 26, 2008 by a Male patient taking Zestoretic (View Usage) (Dosage: 20/25 Mg) . Location: UNITED STATES , 50 years of age, Patient had the following side effects: arthralgia. During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), NORVASC (View Norvasc Review and Norvasc Label ), CLONIDINE (View Clonidine Review and Clonidine Label ).

6152225-5 | Insomnia, Oedema Peripheral, Pruritus, Rash, Swelling Face, Swollen Tongue, Vision Blurred
on Jun 03, 2008 Female patient from UNITED STATES , 69 years of age, weighting 130.1 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: insomnia, oedema peripheral, pruritus, rash (What is rash?), swelling face, swollen tongue, vision blurred. Zestoretic dosage: .

6152223-1 | Abdominal Pain Upper
on Jun 25, 2008 Male patient from UNITED STATES , weighting 213.4 lb, was diagnosed with hypertension, arthritis (What is arthritis?) and was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper. Zestoretic dosage: . During the same period patient was treated with NSAID (View Nsaid Review and Nsaid Label ).

6142577-4 | Asthenia, Condition Aggravated, Dysarthria, Headache, Hypertension, Hypokalaemia, Mental Status Changes
Patient was taking Zestoretic (View Usage). Patient had the following side effects: asthenia, condition aggravated, dysarthria, headache (What is headache?), hypertension, hypokalaemia, mental status changes on Mar 26, 2009 from UNITED STATES Additional patient health information: Female patient , 48 years of age, was diagnosed with hot flush and. Zestoretic dosage: 20/12.5 Mg. During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), LYRICA (View Lyrica Review and Lyrica Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), ABILIFY (View Abilify Review and Abilify Label ), FLUTICASONE PROPIONATE (2 Sprays Daily) (View Fluticasone Propionate Review and Fluticasone Propionate Label ), LORATADINE (View Loratadine Review and Loratadine Label ). Patient was hospitalized.

6135086-X | Orthostatic Hypotension, Renal Failure Acute
Adverse event was reported on Mar 19, 2009 by a Female patient taking Zestoretic (View Usage) (Dosage: 20 + 12.5 Mg Once Daily) was diagnosed with hypertension, polymyalgia rheumatica (What is polymyalgia rheumatica?) and. Location: FRANCE , 72 years of age, After Zestoretic was administered, patient had the following side effects: orthostatic hypotension, renal failure acute. During the same period patient was treated with LERCAN (View Lercan Review and Lercan Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), DIFFU K (View Diffu K Review and Diffu K Label ). Patient was hospitalized.

6107976-5 | Cardio-respiratory Arrest, Hyperkalaemia
on Mar 05, 2009 Male patient from SWITZERLAND , 83 years of age, was diagnosed with pulmonary arterial hypertension and was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, hyperkalaemia. Zestoretic dosage: 12.5/10 Mg. During the same period patient was treated with METFIN (View Metfin Review and Metfin Label ), SERETIDE (View Seretide Review and Seretide Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ).

6073929-9 | Immunoglobulins Increased
on Feb 04, 2009 Female patient from IRELAND , 50 years of age, was treated with Zestoretic (View Usage). Patient had the following side effects: immunoglobulins increased. Zestoretic dosage: . During the same period patient was treated with EMCOR (5 Mg) (View Emcor Review and Emcor Label ), ANXICALM (View Anxicalm Review and Anxicalm Label ), BURINEX (5 Mg) (View Burinex Review and Burinex Label ).

6043519-2 | Dysphagia, Dyspnoea, Eating Disorder, Eye Disorder, Eye Pain, Eye Swelling, Local Swelling, Speech Disorder, Swelling Face
Patient was taking Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: dysphagia, dyspnoea, eating disorder (What is eating disorder?), eye disorder, eye pain, eye swelling, local swelling, speech disorder, swelling face on Jan 14, 2009 from UNITED STATES Additional patient health information: Female patient , 31 years of age, weighting 207.0 lb, was diagnosed with hypertension and. Zestoretic dosage: 10-10.5 Mg 1 Tab Daily Po.

5945992-4 | Blood Pressure Diastolic Increased
Adverse event was reported on Nov 07, 2008 by a Male patient taking Zestoretic (View Usage) (Dosage: 20-12.5mg 1 Tab Qd Po) was diagnosed with hypertension and. Location: UNITED STATES , weighting 198.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure diastolic increased.

5940881-3 | Arthralgia, Back Pain, Hypoaesthesia, Muscle Spasms, Pain In Extremity
on Sep 30, 2008 Male patient from UNITED STATES , 60 years of age, weighting 259.9 lb, was treated with Zestoretic (View Usage). Patient had the following side effects: arthralgia, back pain (What is back pain?), hypoaesthesia, muscle spasms, pain in extremity. Zestoretic dosage: . During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), LORCET HD (View Lorcet-hd Review and Lorcet-hd Label ), IBUPROFEN TABLETS (View Ibuprofen Tablets Review and Ibuprofen Tablets Label ), CELEBREX (View Celebrex Review and Celebrex Label ), LIPITOR (View Lipitor Review and Lipitor Label ), CORTISONE (View Cortisone Review and Cortisone Label ).

5934019-6 | Photosensitivity Reaction
on Oct 20, 2008 Female patient from UNITED STATES , 40 years of age, was diagnosed with hypertension and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: photosensitivity reaction. Zestoretic dosage: .

5920275-7 | Activities Of Daily Living Impaired, Arthralgia, Back Pain, Hypoaesthesia, Muscle Spasms, Pain In Extremity
Patient was taking Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: activities of daily living impaired, arthralgia, back pain (What is back pain?), hypoaesthesia, muscle spasms, pain in extremity on Oct 08, 2008 from UNITED STATES Additional patient health information: Male patient , 52 years of age, weighting 259.9 lb, . Zestoretic dosage: . During the same period patient was treated with LORCET HD (View Lorcet-hd Review and Lorcet-hd Label ), IBUPROFEN TABLETS (View Ibuprofen Tablets Review and Ibuprofen Tablets Label ), CELEBREX (View Celebrex Review and Celebrex Label ), LIPITOR (View Lipitor Review and Lipitor Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

5916780-X | Arthralgia, Back Pain, Hypoaesthesia, Muscle Spasms, Pain In Extremity
Adverse event was reported on Sep 30, 2008 by a Male patient taking Zestoretic (View Usage) (Dosage: ) . Location: UNITED STATES , 60 years of age, weighting 259.9 lb, Patient had the following side effects: arthralgia, back pain (What is back pain?), hypoaesthesia, muscle spasms, pain in extremity. During the same period patient was treated with LORCET HD (View Lorcet-hd Review and Lorcet-hd Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), CELEBREX (View Celebrex Review and Celebrex Label ), LIPITOR (View Lipitor Review and Lipitor Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), CORTISONE (View Cortisone Review and Cortisone Label ).

5880238-7 | Blood Pressure Inadequately Controlled
on Sep 11, 2008 Female patient from UNITED STATES , 67 years of age, weighting 223.0 lb, was diagnosed with hypertension and was treated with Zestoretic (View Usage). After Zestoretic was administered, patient had the following side effects: blood pressure inadequately controlled. Zestoretic dosage: 20/12.5 Daily Po.

5711195-1 | Rash
on Apr 17, 2008 Male patient from UNITED STATES , 66 years of age, weighting 319.0 lb, was treated with Zestoretic (View Usage). Patient experienced the following unwanted or unexpected effects: rash (What is rash?). Zestoretic dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), FLUOCINONIDE (View Fluocinonide Review and Fluocinonide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), CIMETIDINE (View Cimetidine Review and Cimetidine Label ). Patient was hospitalized.

5702445-6 | Alopecia, Blood Pressure Inadequately Controlled
Patient was taking Zestoretic (View Usage). Patient had the following side effects: alopecia, blood pressure inadequately controlled on Sep 12, 2007 from UNITED STATES Additional patient health information: Male patient , 42 years of age, was diagnosed with hypertension, alopecia and. Zestoretic dosage: 10/12.5 Mg. During the same period patient was treated with MICARDIS (View Micardis Review and Micardis Label ), PROPECIA (View Propecia Review and Propecia Label ).

Showing 1-50 of 78  Next Page  >


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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 Zestoretic 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 Zestoretic quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Zestoretic 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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During the same period patient was treated with ZESTORETIC (View Zestoretic Review and Zestoretic Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), FELDENE (View ...

)During the same period patient was treated with CARBOPLATIN, SPECIAFOLDINE, VITAMIN B 12, CORTICOSTEROIDS, ZESTORETIC (1 D/f, Daily (1/d)), TOPALGIC (1 D/f, Daily (1/d)), ...

During the same period patient was treated with VIOXX (Unk) (View Vioxx Review and Vioxx Label ), ARAVA (Unk) (View Arava Review and Arava Label ), ZESTORETIC (View Zestoretic ...

During the same period patient was treated with ZESTORETIC (View Zestoretic Review and Zestoretic Label ). Patient was hospitalized. 7011741-4 | Fatigue

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Zestoretic Reactions
Alopecia
Angioedema
Arthralgia
Asthenia
Back PainWhat is Back pain?
Blood Pressure Inadequately Controlled
Chest PainWhat is Chest pain?
Coronary Artery DiseaseWhat is Coronary artery disease?
Cough
Deafness
Dehydration
DizzinessWhat is Dizziness?
Eye Haemorrhage
FallWhat is Fall?
HeadacheWhat is Headache?
Heart Rate Irregular
Hyperkalaemia
Hypertension
Hypoaesthesia
Hyponatraemia
Hypotension
Interstitial Lung Disease
Muscle Spasms
Nervous System Disorder
Oedema Peripheral
PainWhat is Pain?
Pain In Extremity
Renal Failure
Renal Failure Acute
TinnitusWhat is Tinnitus?
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