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I have developed severe dry cough as a result of using Ramipril for the ...Keep Reading

Can I take ciprofloxacin with my medicines for diabetes...Keep Reading

My partner has just been taken off Ramipril and put on Candesartan ( because ...Keep Reading

Can Ramipril ranbaxy cause itchiness and if so, is it best to ...Keep Reading

My partner takes Ramipril, and now has developed quite severe eneamia. Could ...Keep Reading

my doctor changed me from Ramipril 5mg to Amias 4mg because of developing a ...Keep Reading

Ramipril is excellent - it brings down my pressure. The only issue i ...Keep Reading

I was given Nicorandil for Unstable Angina in conjunction with beta blocker,statins and ....Keep Reading

I have been on Amias for 7 years and have had no side effects ...Keep Reading

I have drowsiness, and continous headache inspite of consuming one ramistar 2.5 ...Keep Reading

Like you I was taking Ramipril 5mg for about 2 yr; I develloped ...Keep Reading

well I get itching legs with it was on 32mg and was really bad ...Keep Reading

I had a thyroidectomy in 1984 at the age of 29 and have been ...Keep Reading

nearly died taking this drug with ramipril didnt know that if i became ill ...Keep Reading

i have a very persistant dry cough which seems worse at night...Keep Reading

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Indicate Your Ramipril Side Effects
Cough (11)
Excess Throat Mucas (9)
Insomnia (8)
Blurred Vision (5)
Arrythmia (2)
Breathless (2)
Diarrhea (2)
>>See All

Common Ramipril Side Effects

top 5 Ramipril|Cough|Excess thr|Insomnia|Blurred vi|Arrythmia|Breathless|Diarrhea adverse effects>>See All Ramipril Side Effects

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Ramipril adverse events reported to FDA.

Have You Experienced unusual Ramipril symptoms? PatientsVille.com collects and analyzes Ramipril side effect and adverse reports submitted by Ramipril users, such as severe hip joint ache Severe bronchitis-type chest|Dry cough exaggerated gagging reflex |very dry cough from consistent to severe.|chemical inbalance |dont know what the days cant remember|.

Summary

FDA Adverse Reports: 559. View All

Ramipril FDA safety alerts: No

Reported deaths: 22

Reported hospitalizations: 318

More About Ramipril

Post Your Unusual Symptoms:

Most Reported
1Cough
2Excess Throat Mucas
3Insomnia
4SORE MUSLE
5Blurred Vision
6Pain In Calf Muscles
7Diarrhea
8Eyes
9Breathless
10Itching
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Recent Drug Reports

severe hip joint ache Severe bronchitis-type chest

Dry cough exaggerated gagging reflex

very dry cough from consistent to severe.

chemical inbalance

dont know what the days cant remember

More Ramipril Side Effect Reports

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

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6831856-0 | Confusional State, Delirium
on Jun 21, 2010 Female patient from UNITED KINGDOM , 75 years of age, was diagnosed with myocardial infarction and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, delirium. Ramipril dosage: 2.5 Mg;po. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), BENDROFLUMETHIAZIDE (BENDROFLUMETHIAZIDE) (View Bendroflumethiazide (bendroflumethiazide) Review and Bendroflumethiazide (bendroflumethiazide) Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), PRACETAMOL (PARACETAMOL) (View Pracetamol (paracetamol) Review and Pracetamol (paracetamol) Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), TIOTROPIUM BROMIDE (TIOTROPIUM BROMIDE) (View Tiotropium Bromide (tiotropium Bromide) Review and Tiotropium Bromide (tiotropium Bromide) Label ). Patient was hospitalized.

6812060-9 | Confusional State, Delirium
Patient was taking Ramipril (View Usage). Patient had the following side effects: confusional state, delirium on Jun 15, 2010 from DENMARK Additional patient health information: Female patient , 75 years of age, was diagnosed with myocardial infarction and. Ramipril dosage: 2.5 Mg; Po. During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), ... (View ... Review and ... Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), TIOTROPIUM (View Tiotropium Review and Tiotropium Label ), BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ). Patient was hospitalized.

6800687-X | Confusional State, Delirium
Adverse event was reported on Jun 15, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 2.5 Mg, Unk) was diagnosed with myocardial infarction and. Location: UNITED KINGDOM , 75 years of age, weighting 167.6 lb, After Ramipril was administered, patient had the following side effects: confusional state, delirium. During the same period patient was treated with ASPIRIN (75 Mg, Unk) (View Aspirin Review and Aspirin Label ), BENDROFLUMETHIAZIDE (2.5 Mg, Unk) (View Bendroflumethiazide Review and Bendroflumethiazide Label ), CLOPIDOGREL (75 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), ACETAMINOPHEN (1 G, Unk) (View Acetaminophen Review and Acetaminophen Label ), SIMVASTATIN (40 Mg, Unk) (View Simvastatin Review and Simvastatin Label ), TIOTROPIUM BROMIDE (18 Ug, Unk) (View Tiotropium Bromide Review and Tiotropium Bromide Label ). Patient was hospitalized.

6795614-8 | Confusional State, Delirium
on Jun 15, 2010 Female patient from UNITED KINGDOM , 75 years of age, weighting 167.6 lb, was diagnosed with myocardial infarction and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, delirium. Ramipril dosage: 2 1/2 Mg, Unk. During the same period patient was treated with ASPIRIN (75 Mg, Unk) (View Aspirin Review and Aspirin Label ), BENDROFLUMETHIAZIDE (2 1/2 Mg, Unk) (View Bendroflumethiazide Review and Bendroflumethiazide Label ), CLOPIDOGREL (75 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), PARACETAMOL (1 G, Unk) (View Paracetamol Review and Paracetamol Label ), SIMVASTATIN (40 Mg, Unk) (View Simvastatin Review and Simvastatin Label ), TIOTROPIUM BROMIDE (18 Mcg, Unk) (View Tiotropium Bromide Review and Tiotropium Bromide Label ). Patient was hospitalized.


6795530-1 | Dysphonia, Eye Swelling, Lip Swelling, Urticaria
on Jun 09, 2010 Male patient from , 57 years of age, was diagnosed with dressler's syndrome and was treated with Ramipril (View Usage). Patient had the following side effects: dysphonia, eye swelling, lip swelling, urticaria. Ramipril dosage: 5 Mg; Po. During the same period patient was treated with ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), HEPARIN (View Heparin Review and Heparin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), MORPHINE (View Morphine Review and Morphine Label ).

6791114-X | Angioedema
Patient was taking Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: angioedema on Jun 22, 2010 from GERMANY Additional patient health information: Male patient , 59 years of age, weighting 275.6 lb, was diagnosed with hypertension and. Ramipril dosage: 1 Df, Qd. During the same period patient was treated with RAMIPRIL+HYDROCHLOROTHIAZIDE (NGX) (1 Df, Qd) (View Ramipril+hydrochlorothiazide (ngx) Review and Ramipril+hydrochlorothiazide (ngx) Label ). Patient was hospitalized.

6786307-1 | Confusional State, Delirium
Adverse event was reported on Jun 15, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 2.5 Mg, Unk) was diagnosed with myocardial infarction and. Location: UNITED KINGDOM , 75 years of age, weighting 167.6 lb, Patient experienced the following unwanted or unexpected effects: confusional state, delirium. During the same period patient was treated with ACETYLSALICYLIC ACID (75 Mg, Unk) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BENDROFLUMETHIAZIDE (2.5 Mg, Unk) (View Bendroflumethiazide Review and Bendroflumethiazide Label ), CLOPIDOGREL (75 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), PARACETAMOL (1 G, Unk) (View Paracetamol Review and Paracetamol Label ), SIMVASTATIN (40 Mg, Unk) (View Simvastatin Review and Simvastatin Label ), TIOTROPIUM BROMIDE (18 Ug, Unk) (View Tiotropium Bromide Review and Tiotropium Bromide Label ). Patient was hospitalized.

6785804-2 | Confusional State, Delirium
on Jun 16, 2010 Female patient from UNITED KINGDOM , 75 years of age, weighting 167.6 lb, was diagnosed with myocardial infarction and was treated with Ramipril (View Usage). Patient had the following side effects: confusional state, delirium. Ramipril dosage: . Patient was hospitalized.

6785519-0 | Dysphonia, Eye Swelling, Lip Swelling, Urticaria
on Jun 09, 2010 Male patient from UNITED KINGDOM , 57 years of age, was diagnosed with dressler's syndrome and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dysphonia, eye swelling, lip swelling, urticaria. Ramipril dosage: 5 Mg, Unk. During the same period patient was treated with ASPIRIN (75 Mg, Unk) (View Aspirin Review and Aspirin Label ), CLOPIDOGREL (150 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), HEPARIN (View Heparin Review and Heparin Label ), METOCLOPRAMIDE (Unk) (View Metoclopramide Review and Metoclopramide Label ), METOPROLOL TARTRATE (50 Mg, Unk) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MORPHINE (View Morphine Review and Morphine Label ), OMNIPAQUE 140 (View Omnipaque 140 Review and Omnipaque 140 Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).

6783242-X | Hypertensive Crisis, Hyponatraemia
Patient was taking Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: hypertensive crisis, hyponatraemia on Jun 08, 2010 from GERMANY Additional patient health information: Female patient , 70 years of age, weighting 136.7 lb, was diagnosed with hypertension, pain (What is pain?), depression (What is depression?), reflux oesophagitis, hypercholesterolaemia, sleep disorder (What is sleep disorder?) and. Ramipril dosage: 10 Mg, Bid. During the same period patient was treated with TELMISARTAN AND HYDROCHLOROTHIAZIDE (1 Df, Qd) (View Telmisartan And Hydrochlorothiazide Review and Telmisartan And Hydrochlorothiazide Label ), TRAMAL/GRUENENTHAL (100 Mg, Tid) (View Tramal/gruenenthal Review and Tramal/gruenenthal Label ), TRIMIPRAMINE (25 Mg, Qd) (View Trimipramine Review and Trimipramine Label ), METOPROLOL TARTRATE (50 Mg, Qd) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PANTOZOL (20 Mg, Qd) (View Pantozol Review and Pantozol Label ), SIMVASTATIN (20 Mg, Qd) (View Simvastatin Review and Simvastatin Label ), ZOLPIDEM (10 Mg, Qd) (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

6782600-7 | Coagulopathy, Hyperkalaemia
Adverse event was reported on Jun 11, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 10 Mg, Unk) was diagnosed with hypertension, hyperlipidaemia, hyperuricaemia, renal failure chronic, atrial fibrillation (What is atrial fibrillation?), pain (What is pain?), constipation (What is constipation?) and. Location: UNITED KINGDOM , 79 years of age, weighting 152.1 lb, Patient had the following side effects: coagulopathy, hyperkalaemia. During the same period patient was treated with SIMVASTATIN (20 Mg, Unk) (View Simvastatin Review and Simvastatin Label ), ALLOPURINOL (150 Mg, Unk) (View Allopurinol Review and Allopurinol Label ), ALDACTONE (50 Mg, Unk) (View Aldactone Review and Aldactone Label ), FALITHROM (3 Mg, Unk) (View Falithrom Review and Falithrom Label ), NORVASC (5 Mg, Unk) (View Norvasc Review and Norvasc Label ), HYDROMORPHONE HCL (8 Mg, Unk) (View Hydromorphone Hcl Review and Hydromorphone Hcl Label ), METOPROLOL SUCCINATE (190 Mg, Unk) (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LACTULOSE (10 Mg, Unk) (View Lactulose Review and Lactulose Label ). Patient was hospitalized.

6782304-0 | Dysphonia, Eye Swelling, Lip Swelling, Urticaria
on Jun 09, 2010 Male patient from UNITED KINGDOM , 57 years of age, was diagnosed with dressler's syndrome and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dysphonia, eye swelling, lip swelling, urticaria. Ramipril dosage: 5 Mg, Unk. During the same period patient was treated with ASPIRIN (75 Mg, Unk) (View Aspirin Review and Aspirin Label ), CLOPIDOGREL (150 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), HEPARIN (View Heparin Review and Heparin Label ), METOCLOPRAMIDE (Unk) (View Metoclopramide Review and Metoclopramide Label ), METOPROLOL TARTRATE (50 Mg, Unk) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MORPHINE (Unk) (View Morphine Review and Morphine Label ), OMNIPAQUE 140 (View Omnipaque 140 Review and Omnipaque 140 Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ).

6768852-8 | Dermatomyositis
on May 03, 2010 Male patient from GERMANY , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: dermatomyositis. Ramipril dosage: 5 Mg, 1 In 1 D, Oral. During the same period patient was treated with COLCHYSAT (COLCHICINE) (View Colchysat (colchicine) Review and Colchysat (colchicine) Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6768582-2 | Hyponatraemia
Patient was taking Ramipril (View Usage). Patient had the following side effects: hyponatraemia on Jun 01, 2010 from GERMANY Additional patient health information: Female patient , 73 years of age, weighting 134.5 lb, was diagnosed with hypertension, tachycardia, hyperlipidaemia, hypothyroidism, ischaemic heart disease prophylaxis and. Ramipril dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), L THYROX (View L-thyrox Review and L-thyrox Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6765523-9 | Hyponatraemia
Adverse event was reported on Jun 08, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: ) was diagnosed with hypertension, depression (What is depression?), pain (What is pain?) and. Location: GERMANY , 70 years of age, weighting 136.7 lb, After Ramipril was administered, patient had the following side effects: hyponatraemia. During the same period patient was treated with TELMISARTAN AND HYDROCHLOROTHIAZIDE (View Telmisartan And Hydrochlorothiazide Review and Telmisartan And Hydrochlorothiazide Label ), TRIMIPRAMINE (View Trimipramine Review and Trimipramine Label ), TRAMADOL HYDROCHLORIDE (View Tramadol Hydrochloride Review and Tramadol Hydrochloride Label ). Patient was hospitalized.

6764638-9 | Hyponatraemia
on Jun 08, 2010 Female patient from GERMANY , 70 years of age, weighting 136.7 lb, was diagnosed with hypertension, pain (What is pain?), depression (What is depression?), reflux oesophagitis, sleep disorder (What is sleep disorder?), hypercholesterolaemia and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia. Ramipril dosage: 10 Mg, Bid. During the same period patient was treated with TELMISARTAN AND HYDROCHLOROTHIAZIDE (1 Df, Qd) (View Telmisartan And Hydrochlorothiazide Review and Telmisartan And Hydrochlorothiazide Label ), TRAMAL (Unk) (View Tramal Review and Tramal Label ), TRIMIPRAMINE (25 Mg, Qd) (View Trimipramine Review and Trimipramine Label ), METOPROLOL TARTRATE (50 Mg, Qd) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PANTOZOL (20 Mg, Qd) (View Pantozol Review and Pantozol Label ), ZOLPIDEM (10 Mg, Qd) (View Zolpidem Review and Zolpidem Label ), SIMVASTATIN (20 Mg, Qd) (View Simvastatin Review and Simvastatin Label ).

6763441-3 | Angioedema, Hypersensitivity, Prurigo
on Jun 07, 2010 Female patient from , 23 years of age, was diagnosed with diabetic nephropathy, type 1 diabetes mellitus and was treated with Ramipril (View Usage). Patient had the following side effects: angioedema, hypersensitivity, prurigo. Ramipril dosage: . During the same period patient was treated with HUMAN INSULIN (View Human Insulin Review and Human Insulin Label ). Patient was hospitalized.

6762148-6 | Dermatomyositis
Patient was taking Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dermatomyositis on Jun 01, 2010 from GERMANY Additional patient health information: Male patient , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension and. Ramipril dosage: . Patient was hospitalized.

6758834-4 | Hyponatraemia
Adverse event was reported on May 31, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 5 Mg, Bid) was diagnosed with hypertension, tachycardia, ischaemic heart disease prophylaxis and. Location: GERMANY , 73 years of age, weighting 134.5 lb, Patient experienced the following unwanted or unexpected effects: hyponatraemia. During the same period patient was treated with AMIODARONE (NGX) (200 Mg, Qd) (View Amiodarone (ngx) Review and Amiodarone (ngx) Label ), ALDACTONE (25 Mg, Qd) (View Aldactone Review and Aldactone Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), L THYROXIN ^HENNING BERLIN^ (View L-thyroxin ^henning Berlin^ Review and L-thyroxin ^henning Berlin^ Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6758121-4 | Dyspnoea, Lethargy, Palpitations
on May 17, 2010 Male patient from UNITED KINGDOM , 62 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient had the following side effects: dyspnoea, lethargy, palpitations. Ramipril dosage: 2.5 Mg; Po. During the same period patient was treated with ALLOPURINOL (View Allopurinol Review and Allopurinol Label ).

6754991-4 | Renal Failure Chronic
on May 14, 2010 Male patient from DENMARK , 75 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: renal failure chronic. Ramipril dosage: 10 Mg;po. During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), PENICILLIN G (View Penicillin G Review and Penicillin G Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ).

6752756-0 | Renal Failure Chronic
Patient was taking Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure chronic on May 13, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 75 years of age, was diagnosed with hypertension and. Ramipril dosage: 10 Mg. During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), PENICILLIN (View Penicillin Review and Penicillin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ).

6745687-3 | Renal Failure Chronic
Adverse event was reported on May 14, 2010 by a Male patient taking Ramipril (View Usage) (Dosage: 10 Mg, Unk) was diagnosed with hypertension and. Location: UNITED KINGDOM , 75 years of age, Patient had the following side effects: renal failure chronic. During the same period patient was treated with AMOXICILLIN (250 Mg, Unk) (View Amoxicillin Review and Amoxicillin Label ), IBUPROFEN (400 Mg, Unk) (View Ibuprofen Review and Ibuprofen Label ), PENICILLIN (250 Mg, Unk) (View Penicillin Review and Penicillin Label ).

6740711-6 | Dyspnoea, Lethargy, Palpitations
on May 05, 2010 Male patient from UNITED KINGDOM , 62 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dyspnoea, lethargy, palpitations. Ramipril dosage: 2.5 Milligram, Oral. During the same period patient was treated with ALLOPURINOL (View Allopurinol Review and Allopurinol Label ).

6740639-1 | Asthenia, Cerebral Atrophy, Cerebral Microangiopathy, Computerised Tomogram Abnormal, Dizziness, Hyponatraemia, Nausea, Sinusitis, Syncope
on May 10, 2010 Female patient from GERMANY , 73 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, cerebral atrophy, cerebral microangiopathy, computerised tomogram abnormal, dizziness (What is dizziness?), hyponatraemia, nausea (What is nausea?), sinusitis (What is sinusitis?), syncope. Ramipril dosage: 5 Mg;bid;po. During the same period patient was treated with SPIRONOLACTONE TABLETS USP (25 Mg;qd;po) (View Spironolactone Tablets Usp Review and Spironolactone Tablets Usp Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6738769-3 | Blood Albumin Decreased, Blood Alkaline Phosphatase Increased, Blood Sodium Decreased, Chills, Dermatitis, Fatigue, Haematocrit Decreased, Haemoglobin Decreased, Platelet Count Increased
Patient was taking Ramipril (View Usage). Patient had the following side effects: blood albumin decreased, blood alkaline phosphatase increased, blood sodium decreased, chills, dermatitis, fatigue, haematocrit decreased, haemoglobin decreased, platelet count increased on May 07, 2010 from UNITED STATES Additional patient health information: Female patient , 67 years of age, weighting 142.2 lb, was diagnosed with hypertension and. Ramipril dosage: 5 Mg;qd. Patient was hospitalized.

6736267-4 | Multi-organ Failure, Toxic Epidermal Necrolysis
Adverse event was reported on May 10, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: Unk) was diagnosed with hyperuricaemia, hypertension and. Location: UNITED KINGDOM , 76 years of age, After Ramipril was administered, patient had the following side effects: multi-organ failure, toxic epidermal necrolysis. During the same period patient was treated with ALLOPURINOL (WATSON LABORATORIES) (150 Mg, Daily) (View Allopurinol (watson Laboratories) Review and Allopurinol (watson Laboratories) Label ), DIAZEPAM (Unk) (View Diazepam Review and Diazepam Label ), CHLORTHALIDONE (WATSON LABORATORIES) (Unk) (View Chlorthalidone (watson Laboratories) Review and Chlorthalidone (watson Laboratories) Label ), OCTATROPINE (Unk) (View Octatropine Review and Octatropine Label ). Patient was hospitalized.

6731041-7 | Dermatomyositis
on May 03, 2010 Male patient from GERMANY , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: dermatomyositis. Ramipril dosage: 5 Mg, 1 In 1 D, Oral. During the same period patient was treated with COLCHYSAT (COLCHICINE) (View Colchysat (colchicine) Review and Colchysat (colchicine) Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6728478-9 | Hyponatraemia
on May 03, 2010 Female patient from GERMANY , 73 years of age, weighting 134.5 lb, was diagnosed with hypertension, tachycardia, hyperlipidaemia, hypothyroidism, ischaemic heart disease prophylaxis and was treated with Ramipril (View Usage). Patient had the following side effects: hyponatraemia. Ramipril dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), L THYROX (View L-thyrox Review and L-thyrox Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6726089-2 | Dyspnoea, Lethargy, Palpitations
Patient was taking Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dyspnoea, lethargy, palpitations on May 05, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 62 years of age, weighting 176.4 lb, was diagnosed with hypertension and. Ramipril dosage: .

6719156-0 | Blood Pressure Increased, Cough
Adverse event was reported on May 11, 2010 by a Male patient taking Ramipril (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 173.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased, cough.

6718696-8 | Chills, Corneal Abscess, Pustular Psoriasis, Pyrexia
on Apr 24, 2010 Female patient from UNITED STATES , 67 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient had the following side effects: chills, corneal abscess, pustular psoriasis, pyrexia. Ramipril dosage: 5 Mg; Qd. Patient was hospitalized.

6716773-9 | Dermatomyositis
on Apr 26, 2010 Male patient from GERMANY , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension, gouty arthritis and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dermatomyositis. Ramipril dosage: 5 Mg, Unk. During the same period patient was treated with COLCHYSAT (0.5 Mg, Unk) (View Colchysat Review and Colchysat Label ), AMLODIPIN 5MG (Unk) (View Amlodipin 5mg Review and Amlodipin 5mg Label ). Patient was hospitalized.

6713963-6 | Hyperkalaemia, Urinary Tract Infection
Patient was taking Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: hyperkalaemia, urinary tract infection (What is urinary tract infection?) on Apr 21, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 61 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and. Ramipril dosage: 10 Mg; Po; Qd. During the same period patient was treated with TRIMETHOPRIM (200 Mg;po;bid) (View Trimethoprim Review and Trimethoprim Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), AMOLODIPINE (View Amolodipine Review and Amolodipine Label ), CITALOPRAM (View Citalopram Review and Citalopram Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), CODEINE SULFATE (View Codeine Sulfate Review and Codeine Sulfate Label ). Patient was hospitalized.

6712414-5 | Choroidal Effusion, Retinal Detachment
Adverse event was reported on Apr 21, 2010 by a Male patient taking Ramipril (View Usage) (Dosage: ) was diagnosed with glomerulonephritis minimal lesion and. Location: GERMANY , 61 years of age, Patient had the following side effects: choroidal effusion, retinal detachment. During the same period patient was treated with CORTISONE (4 Mg, Unk) (View Cortisone Review and Cortisone Label ), CIPROFLOXACIN (View Ciprofloxacin Review and Ciprofloxacin Label ).

6711609-4 | Dermatomyositis
on Apr 26, 2010 Male patient from GERMANY , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: dermatomyositis. Ramipril dosage: . Patient was hospitalized.

6710281-7 | Cardiac Failure, Condition Aggravated, Dyspnoea, Fatigue, Pulmonary Hypertension, Sensation Of Heaviness
on Apr 09, 2010 Female patient from UNITED STATES , 48 years of age, weighting 124.0 lb, was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, condition aggravated, dyspnoea, fatigue, pulmonary hypertension (What is pulmonary hypertension?), sensation of heaviness. Ramipril dosage: 2.5 Mg (1 In 1 D), Per Oral. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), LASIX (View Lasix Review and Lasix Label ), EXJADE (View Exjade Review and Exjade Label ), EVISTA (View Evista Review and Evista Label ), CALCIUM + D (View Calcium + D Review and Calcium + D Label ), FLONASE (View Flonase Review and Flonase Label ), K DUR OR TBCR (View K-dur Or Tbcr Review and K-dur Or Tbcr Label ), M VIT (View M-vit Review and M-vit Label ).

6709956-5 | Cardio-respiratory Arrest, Dehydration, Electrolyte Imbalance, International Normalised Ratio Increased, Prothrombin Time Prolonged
Patient was taking Ramipril (View Usage). Patient had the following side effects: cardio-respiratory arrest, dehydration, electrolyte imbalance, international normalised ratio increased, prothrombin time prolonged on Feb 27, 2009 from GERMANY Additional patient health information: Male patient , 54 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism (What is pulmonary embolism?), chronic obstructive pulmonary disease and. Ramipril dosage: . During the same period patient was treated with BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), FALITHROM ^FAHLBERG^ (Dose As Used: Ziel Inr 2-3) (View Falithrom ^fahlberg^ Review and Falithrom ^fahlberg^ Label ), FURORESE (View Furorese Review and Furorese Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), BEROTEC (Dose As Used: Not Reported) (View Berotec Review and Berotec Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), PREGABALIN (View Pregabalin Review and Pregabalin Label ). Patient was hospitalized.

6709772-4 | Pustular Psoriasis
Adverse event was reported on Apr 29, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 5 Mg) was diagnosed with hypertension, rheumatoid arthritis (What is rheumatoid arthritis?), psoriatic arthropathy and. Location: , 67 years of age, weighting 143.3 lb, After Ramipril was administered, patient had the following side effects: pustular psoriasis. During the same period patient was treated with ADALIMUMAB (View Adalimumab Review and Adalimumab Label ). Patient was hospitalized.

6708829-1 | Acute Abdomen, Angioedema
on Apr 20, 2010 Female patient from BELGIUM , 51 years of age, was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: acute abdomen, angioedema. Ramipril dosage: Unk.

6708734-0 | Renal Impairment
on Apr 20, 2010 Male patient from GERMANY , 79 years of age, weighting 242.5 lb, was diagnosed with hypertension, type 2 diabetes mellitus, hyperuricaemia, acidosis, hypercholesterolaemia and was treated with Ramipril (View Usage). Patient had the following side effects: renal impairment. Ramipril dosage: 5 Mg, Bid. During the same period patient was treated with SPIRONOLACTONE (25 Mg, Unk) (View Spironolactone Review and Spironolactone Label ), ACTOS (15 Mg, Unk) (View Actos Review and Actos Label ), ALLOPURINOL (100 Mg, Unk) (View Allopurinol Review and Allopurinol Label ), AMLODIPINE (5 Mg, Unk) (View Amlodipine Review and Amlodipine Label ), BICANORM (1 G, Unk) (View Bicanorm Review and Bicanorm Label ), LORZAAR (100 Mg, Unk) (View Lorzaar Review and Lorzaar Label ), SIMVABETA (20 Mg, Unk) (View Simvabeta Review and Simvabeta Label ). Patient was hospitalized.

6703277-2 | Angioedema, Throat Tightness
Patient was taking Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: angioedema, throat tightness on Apr 15, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 80 years of age, was diagnosed with myocardial infarction and. Ramipril dosage: 2.5 Mg; Po. During the same period patient was treated with ALENDRONIC ACID (ALENDRONIC ACID) (View Alendronic Acid (alendronic Acid) Review and Alendronic Acid (alendronic Acid) Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ). Patient was hospitalized.

6703276-0 | Chest Discomfort, Dyspnoea, Face Oedema, Rash Pruritic
Adverse event was reported on Apr 15, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: 5 Mg;po;qd) was diagnosed with hypertension and. Location: UNITED KINGDOM , 67 years of age, Patient experienced the following unwanted or unexpected effects: chest discomfort, dyspnoea, face oedema, rash pruritic. During the same period patient was treated with FELODIPINE (View Felodipine Review and Felodipine Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), PENICILLIN NOS (PENICILLIN NOS) (View Penicillin Nos (penicillin Nos) Review and Penicillin Nos (penicillin Nos) Label ).

6701783-8 | Anaphylactic Reaction, Blood Pressure Systolic Increased, Dilatation Ventricular, Pleural Effusion, Pulmonary Hypertension
on Apr 15, 2010 Female patient from GERMANY , 84 years of age, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient had the following side effects: anaphylactic reaction, blood pressure systolic increased, dilatation ventricular, pleural effusion, pulmonary hypertension (What is pulmonary hypertension?). Ramipril dosage: 10 Mg;qd. During the same period patient was treated with ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), GLYCERYL TRINITRATE (View Glyceryl Trinitrate Review and Glyceryl Trinitrate Label ), CANDESARTAN (View Candesartan Review and Candesartan Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), PROCHLORPERAZINE (View Prochlorperazine Review and Prochlorperazine Label ), PALLADONE (View Palladone Review and Palladone Label ). Patient was hospitalized.

6700640-0 | Hyperkalaemia
on Apr 12, 2010 Female patient from UNITED KINGDOM , 61 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: hyperkalaemia. Ramipril dosage: 10 Mg (1 In 1 D), Oral. During the same period patient was treated with TRIMETHOPRIM (200 Mg (2 In 1 D), Oral) (View Trimethoprim Review and Trimethoprim Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), CITALOPRAM (View Citalopram Review and Citalopram Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), CODEINE PHOSPHATE+ PARACETAMOL (CO CODAMOL) (View Codeine Phosphate+ Paracetamol (co-codamol) Review and Codeine Phosphate+ Paracetamol (co-codamol) Label ), ALPHA AMYLASE + AMYLASE+ LIPASE+ PANCREATIN+ PROTEASE (CREON) (View Alpha Amylase + Amylase+ Lipase+ Pancreatin+ Protease (creon) Review and Alpha Amylase + Amylase+ Lipase+ Pancreatin+ Protease (creon) Label ). Patient was hospitalized.

6700478-4 | Chills, Exfoliative Rash, Fatigue, Pustular Psoriasis, Pyrexia, Rash Pruritic, Rash Pustular
Patient was taking Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: chills, exfoliative rash, fatigue, pustular psoriasis, pyrexia, rash pruritic, rash pustular on Apr 19, 2010 from UNITED STATES Additional patient health information: Female patient , 67 years of age, weighting 142.2 lb, was diagnosed with hypertension, psoriatic arthropathy and. Ramipril dosage: 5 Mg/day. During the same period patient was treated with ADALIMUMAB (View Adalimumab Review and Adalimumab Label ). Patient was hospitalized.

6700105-6 | Dysphagia, Pharyngeal Oedema, Swollen Tongue, Thirst
Adverse event was reported on Apr 27, 2010 by a Female patient taking Ramipril (View Usage) (Dosage: Ramipril 2,5 1/day Buccal) was diagnosed with cardiac failure and. Location: UNITED STATES , 85 years of age, weighting 123.0 lb, Patient had the following side effects: dysphagia, pharyngeal oedema, swollen tongue, thirst. During the same period patient was treated with . (View . Review and . Label ). Patient was hospitalized and became disabled.

6699916-5 | Hyperkalaemia
on Apr 14, 2010 Female patient from UNITED KINGDOM , 61 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?), depression (What is depression?) and was treated with Ramipril (View Usage). After Ramipril was administered, patient had the following side effects: hyperkalaemia. Ramipril dosage: 10 Mg, Qd. During the same period patient was treated with TRIMETHOPRIM (200 Mg, Bid) (View Trimethoprim Review and Trimethoprim Label ), AMLODIPINE (5 Mg, Qd) (View Amlodipine Review and Amlodipine Label ), ASPIRIN (75 Mg, Qd) (View Aspirin Review and Aspirin Label ), ATORVASTATIN (40 Mg, Qd) (View Atorvastatin Review and Atorvastatin Label ), CITALOPRAM (10 Mg, Qd) (View Citalopram Review and Citalopram Label ), CLONAZEPAM (500 Ug, Qd) (View Clonazepam Review and Clonazepam Label ), ACETAMINOPHEN AND CODEINE PHOSPHATE (Unk) (View Acetaminophen And Codeine Phosphate Review and Acetaminophen And Codeine Phosphate Label ), CREON (10000 Iu, Prn) (View Creon Review and Creon Label ). Patient was hospitalized.

6699501-5 | Jaundice, Liver Function Test Abnormal
on Apr 27, 2010 Female patient from UNITED STATES , 74 years of age, weighting 160.0 lb, was diagnosed with hypertension and was treated with Ramipril (View Usage). Patient experienced the following unwanted or unexpected effects: jaundice (What is jaundice?), liver function test abnormal. Ramipril dosage: 2.5mg Qd Po.

6698535-4 | Dermatomyositis
Patient was taking Ramipril (View Usage). Patient had the following side effects: dermatomyositis on Apr 26, 2010 from GERMANY Additional patient health information: Male patient , 68 years of age, weighting 229.3 lb, was diagnosed with hypertension and. Ramipril dosage: 5 Mg, Qd. During the same period patient was treated with COLCHYSAT (View Colchysat Review and Colchysat Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

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Ramipril Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

jannette   11201

7:27am on Monday, April 18th, 2011

i'am take a ramipril 5 mg cap (will cost my eyes is so red)?

Flora Isherwood   Location unknown

1:22pm on Friday, November 14th, 2008

I think ramipril caused my feet, legs and ocassionally my mouth to swell

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 Ramipril 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 Ramipril quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ramipril 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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Ramipril Reactions
Acute Myocardial Infarction
Angioedema
Angioneurotic Oedema
Asthenia
Blood Creatinine Increased
Blood Pressure Increased
Bradycardia
Condition Aggravated
Confusional State
Cough
Dehydration
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
Fatigue
HeadacheWhat is Headache?
Hyperkalaemia
Hyponatraemia
Hypotension
Lip Swelling
Malaise
NauseaWhat is Nausea?
Overdose
Palpitations
Presyncope
RashWhat is Rash?
Renal Failure Acute
Swelling Face
Syncope
Vomiting
Ramipril 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 Ramipril 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!