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Ramipril Haemoglobin Decreased Side Effects

Ramipril Haemoglobin Decreased Side Effect Reports


The following Ramipril Haemoglobin Decreased side effect reports were submitted by healthcare professionals and consumers.

This information will help you understand how side effects, such as Haemoglobin Decreased, can occur, and what you can do about them.

A side effect could appear soon after you start Ramipril or it might take time to develop.



Haemoglobin Decreased, International Normalised Ratio Increased, Blood Creatinine Increased

This Haemoglobin Decreased side effect was reported by a health professional from DE. A 76-year-old female patient (weight:NA) experienced the following symptoms/conditions: cardiomyopathy. The patient was prescribed Ramipril (dosage: NA), which was started on 201301. Concurrently used drugs: NA. When starting to take Ramipril the consumer reported the following symptoms:
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
  • Blood Creatinine Increased
The patient was hospitalized. These side effects may potentially be related to Ramipril.
Blood Creatinine Increased, Haemoglobin Decreased, International Normalised Ratio Increased

This Haemoglobin Decreased Ramipril side effect was reported by a physician from DE on Jun 12, 2013. A Female , 76 years of age, was diagnosed with and was treated with Ramipril. The patient presented the following health conditions:
  • Blood Creatinine Increased
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
. Ramipril dosage: Daily Dose: 5 Mg Millgram(s) Every Days. Additional drugs used at the same time:
  • Pradaxa (Daily Dose: 220 Mg Millgram(s) Every Days)
  • Spironolactone (Daily Dose: 25 Mg Millgram(s) Every Days)
  • Torasemid (Daily Dose: 20 Mg Millgram(s) Every Days)
  • Acetylsalicylic Acid (Daily Dose: 100 Mg Millgram(s) Every Days)
The patient was hospitalized.
Blood Creatinine Increased, Haemoglobin Decreased, International Normalised Ratio Increased

This is a Ramipril (ramipril) side effect report of a 76-year-old female patient (weight:NA) from DE, suffering from the following symptoms/conditions: cardiomyopathy,atrial fibrillation, who was treated with Ramipril (ramipril) (dosage:5 Mg (5 Mg, 1 In 1 D), Oral Stopped, start time: 201210), combined with:
  • Pradaxa (220 Mg (110 Mg, 2 In 1 D), Oral?)
  • Spironolactone (spironolactone) (25 Mg (25 Mg, 1 In 1 D), Oral Stopped)
  • Torasemide (torasemide)
  • Acetylsalicylic Acid (acetylsalicylic Acid)
, and developed a serious reaction and a Haemoglobin Decreased side effect. The patient presented with:
  • Blood Creatinine Increased
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Ramipril (ramipril) treatment in female patients suffering from cardiomyopathy,atrial fibrillation, resulting in Haemoglobin Decreased.

Blood Creatinine Increased, Haemoglobin Decreased, International Normalised Ratio Increased

A 76-year-old female patient (weight: NA) from DE with the following symptoms: cardiomyopathy started Ramipril treatment (dosage: NA) on 201301. Soon after starting Ramipril treatment, the consumer experienced several side effects, including:
  • Blood Creatinine Increased
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
. Concurrently used drugs:
  • Spironolactone (spironolactone)
  • Pradaxa (dabigatran Etexilate Mesilate)
  • Torasemide (torasemide)
  • Acetylsalicyclic Acid (acetylsalicylic Acid)
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Ramipril side effects, such as Haemoglobin Decreased.
Blood Creatinine Increased, Haemoglobin Decreased, International Normalised Ratio Increased

A female patient from DE was prescribed and started Ramipril on Jun 06, 2013. Patient felt the following Ramipril side effects: blood creatinine increased, haemoglobin decreased, international normalised ratio increased Additional patient health information: Female , 76 years of age, The consumer reported the following symptoms: was diagnosed with and. Ramipril dosage: 5 Milligram Daily;. Concurrently used drugs:
  • Spironolactone (25 Milligram Daily;)
  • Pradaxa (220 Milligram Daily;)
  • Torasemid (20 Milligram Daily;)
  • Acetylsalicylic Acid (100 Milligram Daily;)
The patient was hospitalized.
Blood Creatinine Increased, Haemoglobin Decreased, International Normalised Ratio Increased

This report suggests a potential Ramipril Haemoglobin Decreased side effect(s) that can have serious consequences. A 76-year-old female patient from DE (weight:NA) was diagnosed with the following health condition(s): cardiomyopathy,atrial fibrillation and used Ramipril (dosage: 5 Mg, 1x/day) starting 201210. Soon after starting Ramipril the patient began experiencing various side effects, including:
  • Blood Creatinine Increased
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
Drugs used concurrently:
  • Pradaxa (110 Mg, 2x/day)
  • Spironolactone (25 Mg, 1x/day)
  • Torasemide (20 Mg, 1x/day)
  • Acetylsalicylic Acid (100 Mg, 1x/day)
The patient was hospitalized. Although Ramipril demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Haemoglobin Decreased, may still occur.
International Normalised Ratio Increased, Blood Creatinine Increased, Haemoglobin Decreased

An adverse event was reported by a health professional on Jun 05, 2013 by a Female taking Ramipril (dosage: 5 Mg, Qd) was diagnosed with and. Location: DE , 76 years of age, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Ramipril side effects: international normalised ratio increased, blood creatinine increased, haemoglobin decreased. Additional medications/treatments:
Associated medications used:
  • Spironolacton (25 Mg, Qd)
  • Pradaxa (110 Mg, Bid)
  • Torasemid (20 Mg, Qd)
  • Acetylsalicylic Acid (100 Mg, Qd)
The patient was hospitalized.
Febrile Neutropenia, Diarrhoea, Haemoglobin Decreased, Red Blood Cell Sedimentation Rate Increased, White Blood Cell Count Decreased, Neutrophil Count Decreased

This Haemoglobin Decreased problem was reported by a consumer or non-health professional from COUNTRY NOT SPECIFIED. A 75-year-old patient (weight: NA) was diagnosed with the following medical condition(s): NA.On NS a consumer started treatment with Ramipril (ramipril) (dosage: NA). The following drugs/medications were being taken at the same time:
  • Tamsulosin (tamsulosin) (10 Mg (10 Mg, 1 In 1 D) , Oral)
  • Omeprazole (omeprazole)
  • Amlodipine (amlodipine)
  • Atorvastatin (atorvastatin)
  • Docetaxel (docetaxel)?
  • Mirtazapine (mirtazapine)
  • Timolol (timolol) (none)
  • Zoladex (goserelin)
When commencing Ramipril (ramipril), the patient experienced the following unwanted symptoms /side effects:
  • Febrile Neutropenia
  • Diarrhoea
  • Haemoglobin Decreased
  • Red Blood Cell Sedimentation Rate Increased
  • White Blood Cell Count Decreased
  • Neutrophil Count Decreased
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Haemoglobin Decreased, may become evident only after a product is in use by the general population.
Febrile Neutropenia, Diarrhoea, Pyrexia, White Blood Cell Count Decreased, Neutrophil Count Decreased, Haemoglobin Decreased, Red Blood Cell Sedimentation Rate Increased

This is a Ramipril side effect report of a 75-year-old patient (weight: NA) from GB. The patient developed the following symptoms/conditions: NA and was treated with Ramipril (dosage: 10 Mg, 1x/day) starting Jan 14, 2013. Concurrently used drugs:
  • Tamsulosin (400 Ug, 1x/day)
  • Omeprazole (20 Mg, 1x/day)
  • Zoladex
  • Docetaxel
  • Mirtazapine
  • Atorvastatin
  • Amlodipine
  • Timolol (0.5 %, Unk)
Soon after that, the consumer experienced the following of symptoms:
  • Febrile Neutropenia
  • Diarrhoea
  • Pyrexia
  • White Blood Cell Count Decreased
  • Neutrophil Count Decreased
  • Haemoglobin Decreased
  • Red Blood Cell Sedimentation Rate Increased
The patient was hospitalized. This opens a possibility that Ramipril could cause Haemoglobin Decreased and that some patients may be more susceptible.
Febrile Neutropenia, Red Blood Cell Sedimentation Rate Increased, Haemoglobin Decreased, White Blood Cell Count Decreased, Neutrophil Count Decreased, Pyrexia, Diarrhoea

This Haemoglobin Decreased side effect was reported by a health professional from GB on Feb 11, 2014. A patient from GB , 75 years of age, weighting 178.6 lb, was treated with Ramipril. Directly after treatment started, patient experienced the unwanted or unexpected Ramipril side effects: febrile neutropenia, red blood cell sedimentation rate increased, haemoglobin decreased, white blood cell count decreased, neutrophil count decreased, pyrexia, diarrhoea. Ramipril dosage: 10 Mg Daily.
Associated medications used:
  • Tamsulosin (400 Ug Daily)
  • Omeprazole (20 Mg Daily)
  • Zoladex (11.25 Mg)
  • Docetaxel (120 Mg)
  • Mirtazapine
  • Atorvastatin
  • Amlodipine
  • Timolol (0.5 %)
The patient was hospitalized. These side effects may potentially be related to Ramipril.
Febrile Neutropenia, Diarrhoea, Pyrexia, White Blood Cell Count Decreased, Neutrophil Count Decreased, Haemoglobin Decreased, Red Blood Cell Sedimentation Rate Increased

This Haemoglobin Decreased side effect was reported by a physician from GB. A 75-year-old patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Ramipril (dosage: 10 Mg, 1x/day), which was started on Jan 14, 2013. Concurrently used drugs:
  • Tamsulosin Hydrochloride (400 Ug, 1x/day)
  • Omeprazole (20 Mg, 1x/day)
  • Zoladex (11.25 Mg, Unk)
  • Docetaxel (120 Mg, Unk)
  • Mirtazapine (Unk)
  • Atorvastatin (Unk)
  • Amlodipine (Unk)
  • Timolol (0.5 %, Unk)
When starting to take Ramipril the consumer reported the following symptoms:
  • Febrile Neutropenia
  • Diarrhoea
  • Pyrexia
  • White Blood Cell Count Decreased
  • Neutrophil Count Decreased
  • Haemoglobin Decreased
  • Red Blood Cell Sedimentation Rate Increased
The patient was hospitalized. These side effects may potentially be related to Ramipril.
Red Blood Cell Abnormality, Anaemia, White Blood Cell Disorder, Aplasia Pure Red Cell, Lethargy, Cardiac Failure, Haemoglobin Decreased, Histiocytosis Haematophagic, Megakaryocytes Increased

This Haemoglobin Decreased Ramipril side effect was reported by a pharmacist from UNITED KINGDOM on Jun 21, 2012. A male , 31 years of age, was diagnosed with and was treated with Ramipril. The patient presented the following health conditions:
  • Red Blood Cell Abnormality
  • Anaemia
  • White Blood Cell Disorder
  • Aplasia Pure Red Cell
  • Lethargy
  • Cardiac Failure
  • Haemoglobin Decreased
  • Histiocytosis Haematophagic
  • Megakaryocytes Increased
. Ramipril dosage: 5 Mg Daily. Additional drugs used at the same time:
  • Atripla (1 Df Daily)
The patient was hospitalized.
Lethargy, Dyspnoea, Megakaryocytes Increased, Aplasia Pure Red Cell, Histiocytosis Haematophagic, Haemoglobin Decreased, Anaemia, Bone Marrow Disorder, Cardiac Failure

This is a Ramipril side effect report of a 31-year-old patient (weight:NA) from UNITED KINGDOM, suffering from the following symptoms/conditions: hypertension,hiv infection, who was treated with Ramipril (dosage:5 Mg, 1x/day, start time: Dec 01, 2011), combined with:
  • Atripla (1 Df, 1x/day)
, and developed a serious reaction and a Haemoglobin Decreased side effect. The patient presented with:
  • Lethargy
  • Dyspnoea
  • Megakaryocytes Increased
  • Aplasia Pure Red Cell
  • Histiocytosis Haematophagic
  • Haemoglobin Decreased
  • Anaemia
  • Bone Marrow Disorder
  • Cardiac Failure
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Ramipril treatment in patients suffering from hypertension,hiv infection, resulting in Haemoglobin Decreased.
Haemoglobin Decreased, Haematemesis, Duodenal Ulcer, Melaena

A 72-year-old female patient (weight: NA) from UNITED KINGDOM with the following symptoms: NA started Ramipril treatment (dosage: NA) on Dec 21, 2011. Soon after starting Ramipril treatment, the consumer experienced several side effects, including:
  • Haemoglobin Decreased
  • Haematemesis
  • Duodenal Ulcer
  • Melaena
. Concurrently used drugs:
  • Albuterol
  • Lactulose
  • Fostair
  • Naproxen
  • Bendroflumethiazide
  • Quinine Sulfate
  • Senna-mint Waf (As Necessary)
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Ramipril side effects, such as Haemoglobin Decreased.
Lethargy, White Blood Cell Disorder, Histiocytosis Haematophagic, Cardiac Failure, Bone Marrow Disorder, Haemoglobin Decreased, Red Blood Cell Abnormality, Megakaryocytes Increased, Aplasia Pure Red Cell

A female patient from UNITED KINGDOM was prescribed and started Ramipril on May 22, 2012. After Ramipril was administered, patient encountered several Ramipril side effects: lethargy, white blood cell disorder, histiocytosis haematophagic, cardiac failure, bone marrow disorder, haemoglobin decreased, red blood cell abnormality, megakaryocytes increased, aplasia pure red cell Additional patient health information: Female , 31 years of age, The consumer reported the following symptoms: was diagnosed with and. Ramipril dosage: 5 Mg, Daily. Concurrently used drugs:
  • Atripla (1 Df, Daily)
The patient was hospitalized.
Anaemia, Haemoglobin Decreased, Cardiac Failure, Red Blood Cell Abnormality, White Blood Cell Disorder, Dyspnoea, Histiocytosis Haematophagic, Aplasia Pure Red Cell, Lethargy

This report suggests a potential Ramipril Haemoglobin Decreased side effect(s) that can have serious consequences. A 31-year-old female patient from UNITED KINGDOM (weight:NA) was diagnosed with the following health condition(s): hypertension,hiv infection and used Ramipril (dosage: 5 Mg, Qd) starting Dec 01, 2011. Soon after starting Ramipril the patient began experiencing various side effects, including:
  • Anaemia
  • Haemoglobin Decreased
  • Cardiac Failure
  • Red Blood Cell Abnormality
  • White Blood Cell Disorder
  • Dyspnoea
  • Histiocytosis Haematophagic
  • Aplasia Pure Red Cell
  • Lethargy
Drugs used concurrently:
  • Atripla (1 Df, Qd)
The patient was hospitalized. Although Ramipril demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Haemoglobin Decreased, may still occur.
Dyspnoea, Chest Pain, Haemoglobin Decreased, Lethargy, Aplasia Pure Red Cell, Bone Marrow Disorder, White Blood Cell Disorder, Histiocytosis Haematophagic, Red Blood Cell Abnormality

An adverse event was reported by a pharmacist on May 22, 2012 by a Female taking Ramipril (dosage: NA) was diagnosed with and. Location: UNITED KINGDOM , 31 years of age, patient began experiencing various side effects, including: Patient felt the following Ramipril side effects: dyspnoea, chest pain, haemoglobin decreased, lethargy, aplasia pure red cell, bone marrow disorder, white blood cell disorder, histiocytosis haematophagic, red blood cell abnormality. Additional medications/treatments:
Multiple prescriptions taken:
  • Atripla
The patient was hospitalized.
Dyspnoea, Haemoglobin Decreased, Megakaryocytes Increased, Cardiac Failure, Aplasia Pure Red Cell, Histiocytosis Haematophagic, Chest Pain, Lethargy, Red Blood Cell Abnormality

This Haemoglobin Decreased problem was reported by a pharmacist from UNITED KINGDOM. A 31-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): hypertension,hiv infection.On Dec 01, 2011 a consumer started treatment with Ramipril (dosage: NA). The following drugs/medications were being taken at the same time:
  • Atripla
When commencing Ramipril, the patient experienced the following unwanted symptoms /side effects:
  • Dyspnoea
  • Haemoglobin Decreased
  • Megakaryocytes Increased
  • Cardiac Failure
  • Aplasia Pure Red Cell
  • Histiocytosis Haematophagic
  • Chest Pain
  • Lethargy
  • Red Blood Cell Abnormality
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Haemoglobin Decreased, may become evident only after a product is in use by the general population.
Syncope, Blood Urea Increased, Hyperkalaemia, Haemoglobin Decreased, Blood Creatinine Increased, Hypotension

This is a Ramipril side effect report of a 83-year-old patient (weight: NA) from ITALY. The patient developed the following symptoms/conditions: hypertension and was treated with Ramipril (dosage: 10 Mg, Once) starting Jun 01, 2010. Concurrently used drugs:
  • Casodex (Unk)
  • Metformin Hydrochloride (2 Units, 1x/day)
  • Warfarin Sodium (5 Mg, 1x/day)
  • Amitriptyline Hcl (Unk)
Soon after that, the consumer experienced the following of symptoms:
  • Syncope
  • Blood Urea Increased
  • Hyperkalaemia
  • Haemoglobin Decreased
  • Blood Creatinine Increased
  • Hypotension
The patient was hospitalized. This opens a possibility that Ramipril could cause Haemoglobin Decreased and that some patients may be more susceptible.
Haemoglobin Decreased, Myelodysplastic Syndrome, White Blood Cell Count Decreased

This Haemoglobin Decreased side effect was reported by a health professional from UNITED KINGDOM on Mar 14, 2012. A patient from UNITED KINGDOM , 80 years of age, was diagnosed with and was treated with Ramipril. Patient felt the following Ramipril side effects: haemoglobin decreased, myelodysplastic syndrome, white blood cell count decreased. Ramipril dosage: 1.25 Mg, 1x/day.
Multiple prescriptions taken:
  • Levothyroxine (25 Ug, 1x/day)
  • Tamsulosin (400 Ug, 1x/day)
  • Isopropyl Myristate And Paraffin, Liquid (Unk)
  • Lamotrigine (25 Mg, 1x/day)
  • Latanoprost (50 Ug/ml, Unk)
  • Finasteride (5 Mg, 1x/day)
  • Warfarin (As Per Inr)
These side effects may potentially be related to Ramipril.
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DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Ramipril Haemoglobin Decreased Causes and Reviews


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Ramipril Haemoglobin Decreased Reviews

Sat, 05 Jan 2013

Have been taken off Ramipril... I was on 7.5mg. First I had the cough and servere tingling in the face and legs. Then came the puffiness that was gradual. Feeling generally unwell. I have been off Ramipril for the past 3 weeks. Just on felodpine 2.5mg at the moment my bp is around 125/80 in the past went up to 180/111. I have lost 2.1/2 stone in weight I am 66years of age. The only problem now is I still fill edgy, still some tingling in my face puffiness has gone.  I do feel that Ramipril needs to be looked at more carefully. As do other bp tablets... Seems to me they can do more harm than good in some people.

Sat, 08 Jun 2013

I have just woke up again cant bear pain in wrist and thumb came on overnight, as well as swollen feet, wheezing, dizzyness all started 3-4 months after being presicribed RAMPRIL always feel ill after taking it. Docs monday not taking it any more its dangerous.

Sun, 06 May 2012

Ramipril is horrible, my symptoms shaky, passing out, off balance, very low BP 80/40, stomach pain , numbness in hands and feet, rash, bad cough. My doctor told me to drink tomato juice and i will be ok. thats was when i stopped taken it and fired my doctor

Mon, 09 May 2011

I have been taking Rampril Hexal 5mg tablet evry day for the last about one month. It does not seem to lower down my blood pressure which is about 160/90. At the same time I have started feeling weakness in my legs - upper thighs - while climbinga few stairs.

Wed, 03 Aug 2011

i have been on Ramipril for a year and a half,( 2.5) i have congenital aortic stenosis,which has caused my bp to go up, for the past 8 months or so i have gotten bladder pain, lower abdominal pain which is worse when i lie down to rest, awful back pain, i have had lots of scans, blood tests, one doctor i had refused to do any more tests, he turned his back on me when i was in sooo much pain,(i got another doctor) i have seen a gynecologist, all was well.. i have an appointment with an urologist next month.. all my tests have come back OK except i always have blood in my urine???..anyway i was talking to my pharmacist, and he said that this may be caused by by Ramipril, this could be a very rare side effect.. so i called my cardiologist, talked to his receptionist and i will be switching bp meds in a few days (he is out of town) i will keep you informed as to what happens.. how old is this drug ? i do not want to be a guinea pig for these drug companies....

Tue, 15 Nov 2011

My Mother was put on Ramipril for hghi BP, soon she developed really bad cough, when we went back to the doctor she advised my Mother to stop smocking and recomended Xray for her lungs, came back ok, later when the cough got worst the dr.diagnosed COPD and prescribed Advair plus all other paffers, they did not bring much relief and I foud it strainge cose I have asma and all the "paffers" are my life line, they work wonders.Soon my Mother develop breast cancer and died.When she died there was a large bottle of Ramipril left and I decided to use it becouse my BP is olso high, after taking Ramipril for two, maybe tree days I had the same horrible spazmatic cough,I though"OMG I am sounding like my Mother and then I just new,I never took that med.again, I am doing well on Norvasc, but I have no dout about this side effect and I just wander why so many doctors we have seen in the meantime and no one had a clue,or they don't care especiali when you are a smoker.

Fri, 14 Nov 2008
I think Ramipril caused my feet, legs and ocassionally my mouth to swell
Mon, 18 Apr 2011
i'am take a Ramipril 5 mg cap (will cost my eyes is so red)?
DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

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Top Ramipril Side Effects

Renal Failure Acute (252)
Dyspnoea (156)
Angioedema (149)
Hypotension (148)
Dizziness (130)
Cough (125)
Dehydration (107)
Nausea (105)
Hyperkalaemia (104)
Hyponatraemia (97)
Diarrhoea (95)
Confusional State (91)
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Vomiting (87)
Malaise (85)
Fall (82)
Fatigue (78)
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Headache (77)
Asthenia (75)
Swollen Tongue (65)
Lip Swelling (64)
Blood Pressure Increased (63)
Blood Creatinine Increased (62)
Cardiac Failure (62)
Hypoaesthesia (61)
Pruritus (58)
Palpitations (55)
Renal Failure (55)
Loss Of Consciousness (54)
Hypertension (52)
Haemoglobin Decreased (48)
Atrial Fibrillation (47)
Condition Aggravated (47)
Somnolence (45)
Pain In Extremity (44)
Paraesthesia (43)
Rash (42)
Abdominal Pain (41)
Hyperhidrosis (39)
Overdose (38)
Pneumonia (38)
International Normalised Ratio Increased (38)
Depression (37)
Vision Blurred (36)
Renal Impairment (36)
Lactic Acidosis (36)
Bradycardia (36)
Sepsis (35)
Myalgia (35)

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