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Nifedipine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 659. View All

Nifedipine FDA safety alerts: No

Reported deaths: 113

Reported hospitalizations: 274

Nifedipine Dosage, Warnings, Usage.

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

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7027120-X | Eosinophilic Pneumonia, Interstitial Lung Disease, Lymphocyte Stimulation Test Positive, Organising Pneumonia, Pharyngeal Oedema, Tachycardia
on Sep 13, 2010 Female patient from JAPAN , 54 years of age, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: eosinophilic pneumonia, interstitial lung disease, lymphocyte stimulation test positive, organising pneumonia, pharyngeal oedema, tachycardia. Nifedipine dosage: . During the same period patient was treated with HAKUMOUNTOU (View Hakumountou Review and Hakumountou Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ), BAKUMONDOTO (View Bakumondoto Review and Bakumondoto Label ), ETIZOLAM (View Etizolam Review and Etizolam Label ). Patient was hospitalized.

7023191-5 | Fatigue, Hypertension, Oedema Peripheral, Thyroid Neoplasm
Patient was taking Nifedipine (View Usage). Patient had the following side effects: fatigue, hypertension, oedema peripheral, thyroid neoplasm on Sep 22, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 174.2 lb, was diagnosed with hypertension, cerebrovascular accident prophylaxis and. Nifedipine dosage: 30 Mg, Daily. During the same period patient was treated with ATENOLOL (30 Mg, Daily) (View Atenolol Review and Atenolol Label ).

7021976-2 | Blood Lactic Acid Increased, Blood Phosphorus Increased, Depressed Level Of Consciousness, Diarrhoea, Hyperkalaemia, Renal Failure Acute
Adverse event was reported on Aug 12, 2010 by a Male patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with colonoscopy (What is colonoscopy?) and. Location: HONG KONG , 75 years of age, After Nifedipine was administered, patient had the following side effects: blood lactic acid increased, blood phosphorus increased, depressed level of consciousness, diarrhoea, hyperkalaemia, renal failure acute. During the same period patient was treated with GLICLAZIDE NOS (View Gliclazide Nos Review and Gliclazide Nos Label ), SOTALOL (View Sotalol Review and Sotalol Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), SODIUM PHOSPHATE (View Sodium Phosphate Review and Sodium Phosphate Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), METFORMIN (View Metformin Review and Metformin Label ). Patient was hospitalized.

7005173-2 | Gingival Hyperplasia
on Sep 20, 2010 Male patient from UNITED STATES , 55 years of age, weighting 205.0 lb, was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: gingival hyperplasia. Nifedipine dosage: 120 Mg Every Day Po.


6988450-0 | Cough, Intestinal Obstruction, Memory Impairment, Oedema Peripheral
on Sep 08, 2010 Male patient from ISRAEL , 83 years of age, was treated with Nifedipine (View Usage). Patient had the following side effects: cough, intestinal obstruction, memory impairment, oedema peripheral. Nifedipine dosage: . Patient was hospitalized.

6979402-5 | Micturition Disorder
Patient was taking Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: micturition disorder on Sep 10, 2010 from UNITED STATES Additional patient health information: Female patient , 64 years of age, weighting 158.0 lb, was diagnosed with blood pressure decreased and. Nifedipine dosage: 60 Mg One Tab Daily.

6957028-7 | Hyperhidrosis, Palpitations
Adverse event was reported on Aug 27, 2010 by a Female patient taking Nifedipine (View Usage) (Dosage: 90mg Qday Po 1 Dose) was diagnosed with hypertension and. Location: UNITED STATES , 73 years of age, Patient experienced the following unwanted or unexpected effects: hyperhidrosis, palpitations. Patient was hospitalized.

6867546-8 | Atrioventricular Dissociation, Blood Pressure Decreased, Confusional State, Depressed Level Of Consciousness
on Jul 13, 2010 Female patient from UNITED STATES , 52 years of age, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient had the following side effects: atrioventricular dissociation, blood pressure decreased, confusional state, depressed level of consciousness. Nifedipine dosage: . During the same period patient was treated with CLONIDINE (View Clonidine Review and Clonidine Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ).

6837257-3 | International Normalised Ratio Increased, Peripheral Coldness, Post Procedural Haemorrhage, Tooth Extraction
on Jun 24, 2010 Male patient from UNITED KINGDOM , 48 years of age, was diagnosed with peripheral coldness and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: international normalised ratio increased, peripheral coldness, post procedural haemorrhage, tooth extraction. Nifedipine dosage: 5 Mg; Tid; Po. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ). Patient was hospitalized.

6817685-2 | Blood Pressure Increased, Fatigue, Nodule, Oedema Peripheral
Patient was taking Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, fatigue, nodule, oedema peripheral on Jun 24, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 175.0 lb, was diagnosed with hypertension, cerebrovascular accident prophylaxis and. Nifedipine dosage: 30 Mg, Daily. During the same period patient was treated with ATENOLOL (30 Mg, Daily) (View Atenolol Review and Atenolol Label ).

6805453-7 | Blood Pressure Inadequately Controlled
Adverse event was reported on Nov 29, 2007 by a Female patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 77 years of age, Patient had the following side effects: blood pressure inadequately controlled. During the same period patient was treated with METOPROLOL (View Metoprolol Review and Metoprolol Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ), DIGOXIN (View Digoxin Review and Digoxin Label ).

6805252-6 | Product Quality Issue
on Sep 24, 2007 Female patient from UNITED STATES , 55 years of age, was diagnosed with hypertension and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: product quality issue. Nifedipine dosage: .

6805174-0 | Muscle Spasms, Myalgia
on Oct 26, 2007 Female patient from UNITED STATES , 71 years of age, weighting 143.0 lb, was diagnosed with cardiac disorder and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: muscle spasms, myalgia. Nifedipine dosage: .

6805035-7 | Feeling Abnormal
Patient was taking Nifedipine (View Usage). Patient had the following side effects: feeling abnormal on Aug 06, 2007 from UNITED STATES Additional patient health information: Female patient , 78 years of age, was diagnosed with hypertension and. Nifedipine dosage: .

6805018-7 | Blood Pressure Inadequately Controlled
Adverse event was reported on Aug 07, 2007 by a Male patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 68 years of age, After Nifedipine was administered, patient had the following side effects: blood pressure inadequately controlled. During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6805007-2 | Constipation, Eye Pruritus, Lacrimation Increased, Rash Pruritic, Vision Blurred
on Jul 25, 2007 Female patient from UNITED STATES , 87 years of age, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), eye pruritus, lacrimation increased, rash pruritic, vision blurred. Nifedipine dosage: . During the same period patient was treated with AVALIDE (View Avalide Review and Avalide Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

6804982-X | Blood Pressure Inadequately Controlled
on Aug 03, 2007 Female patient from UNITED STATES , 86 years of age, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient had the following side effects: blood pressure inadequately controlled. Nifedipine dosage: . During the same period patient was treated with COREG (View Coreg Review and Coreg Label ), DIGITALIS TAB (View Digitalis Tab Review and Digitalis Tab Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

6804343-3 | Blood Pressure Inadequately Controlled
Patient was taking Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: blood pressure inadequately controlled on Feb 28, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 158.0 lb, . Nifedipine dosage: . During the same period patient was treated with ATORVASTATIN CALCIUM (Once Daily) (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ).

6804263-4 | Abdominal Distension, Dyspepsia, Foreign Body, Nausea
Adverse event was reported on Mar 06, 2007 by a Male patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 75 years of age, Patient experienced the following unwanted or unexpected effects: abdominal distension, dyspepsia, foreign body, nausea (What is nausea?). During the same period patient was treated with ENALAPRIL MALEATE (View Enalapril Maleate Review and Enalapril Maleate Label ), LABETALOL HYDROCHLORIDE (View Labetalol Hydrochloride Review and Labetalol Hydrochloride Label ).

6804144-6 | Abdominal Pain Upper, Blood Pressure Inadequately Controlled, Chest Pain, Dizziness, Tremor, Vision Blurred
on Dec 28, 2007 Female patient from UNITED STATES , weighting 125.0 lb, was diagnosed with chest pain (What is chest pain?), cardiac disorder, hypertension, blood cholesterol increased and was treated with Nifedipine (View Usage). Patient had the following side effects: abdominal pain upper, blood pressure inadequately controlled, chest pain (What is chest pain?), dizziness (What is dizziness?), tremor, vision blurred. Nifedipine dosage: . During the same period patient was treated with PROCARDIA XL (Qd: Every Day) (View Procardia Xl Review and Procardia Xl Label ), LIPITOR (Daily: Every Day) (View Lipitor Review and Lipitor Label ), CALCIUM (View Calcium Review and Calcium Label ), PRILOSEC (View Prilosec Review and Prilosec Label ). Patient was hospitalized.

6804133-1 | Oedema Peripheral, Rash
on Feb 15, 2007 Male patient from UNITED STATES , 72 years of age, was diagnosed with ill-defined disorder and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: oedema peripheral, rash (What is rash?). Nifedipine dosage: Once Daily. During the same period patient was treated with EZETIMIBE (Once Daily) (View Ezetimibe Review and Ezetimibe Label ), GLIPIZIDE (Once Daily) (View Glipizide Review and Glipizide Label ).

6800848-X | Blood Pressure Inadequately Controlled, Insomnia, Nightmare, Suffocation Feeling
Patient was taking Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure inadequately controlled, insomnia, nightmare, suffocation feeling on Jul 16, 2007 from UNITED STATES Additional patient health information: Female patient , 85 years of age, weighting 155.0 lb, was diagnosed with hypertension and. Nifedipine dosage: . During the same period patient was treated with COLCHICINE (Qd) (View Colchicine Review and Colchicine Label ), HYDROCHLOROTHIAZIDE (Weekly) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6797782-0 | Burning Sensation, Dizziness, Headache, Palpitations, Tremor
Adverse event was reported on Jun 10, 2010 by a Female patient taking Nifedipine (View Usage) (Dosage: 10 Mg; Po) was diagnosed with raynaud's phenomenon and. Location: DENMARK , 28 years of age, Patient had the following side effects: burning sensation, dizziness (What is dizziness?), headache (What is headache?), palpitations, tremor. During the same period patient was treated with CEFRADINE (View Cefradine Review and Cefradine Label ), COLPERMIN (View Colpermin Review and Colpermin Label ), MEBEVERINE (View Mebeverine Review and Mebeverine Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6797782-0 | Burning Sensation, Dizziness, Headache, Palpitations, Tremor
on Jun 10, 2010 Female patient from DENMARK , 28 years of age, was diagnosed with raynaud's phenomenon and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: burning sensation, dizziness (What is dizziness?), headache (What is headache?), palpitations, tremor. Nifedipine dosage: 10 Mg; Po. During the same period patient was treated with CEFRADINE (View Cefradine Review and Cefradine Label ), COLPERMIN (View Colpermin Review and Colpermin Label ), MEBEVERINE (View Mebeverine Review and Mebeverine Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6792915-4 | Blood Pressure Inadequately Controlled
on Oct 24, 2008 Female patient from UNITED STATES , weighting 119.9 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure inadequately controlled. Nifedipine dosage: .

6792563-6 | Blood Pressure Fluctuation, Blood Pressure Systolic Increased
Patient was taking Nifedipine (View Usage). Patient had the following side effects: blood pressure fluctuation, blood pressure systolic increased on Aug 11, 2008 from UNITED STATES Additional patient health information: Female patient , 83 years of age, was diagnosed with hypertension and. Nifedipine dosage: . During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ), HYZAAR (View Hyzaar Review and Hyzaar Label ), LANOXIN (View Lanoxin Review and Lanoxin Label ).

6792337-6 | Blood Pressure Increased
Adverse event was reported on Aug 12, 2008 by a Female patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 57 years of age, After Nifedipine was administered, patient had the following side effects: blood pressure increased. During the same period patient was treated with LEXAPRO (View Lexapro Review and Lexapro Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ).

6792076-1 | Insomnia, Nervousness
on Jul 22, 2008 Male patient from UNITED STATES , 77 years of age, was diagnosed with hypertension, dyspnoea, gastrooesophageal reflux disease, blood cholesterol increased, osteopenia and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: insomnia, nervousness. Nifedipine dosage: . During the same period patient was treated with THEOPHYLLINE (View Theophylline Review and Theophylline Label ), POTASSIUM (View Potassium Review and Potassium Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), LIPITOR (View Lipitor Review and Lipitor Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ).

6792021-9 | Blood Pressure Fluctuation
on Aug 05, 2008 Male patient from UNITED STATES , 52 years of age, weighting 170.0 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient had the following side effects: blood pressure fluctuation. Nifedipine dosage: .

6791492-1 | Oedema Peripheral
Patient was taking Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: oedema peripheral on Jul 10, 2008 from UNITED STATES Additional patient health information: Female patient , 77 years of age, weighting 160.0 lb, was diagnosed with hypertension and. Nifedipine dosage: . During the same period patient was treated with OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), HYDROCHLOROTHIAZIDE (2 Every 1 Weeks) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), COZAAR (View Cozaar Review and Cozaar Label ).

6790604-3 | Decreased Appetite, Palpitations, Weight Decreased
Adverse event was reported on May 14, 2008 by a Female patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension, ear infection (What is ear infection?) and. Location: UNITED STATES , 58 years of age, Patient experienced the following unwanted or unexpected effects: decreased appetite, palpitations, weight decreased. During the same period patient was treated with LEVAQUIN (View Levaquin Review and Levaquin Label ), XANAX (Prn) (View Xanax Review and Xanax Label ).

6788939-3 | Dyspepsia, Fatigue, Pyrexia, Urinary Tract Infection
on May 23, 2008 Female patient from UNITED STATES , 70 years of age, weighting 133.0 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient had the following side effects: dyspepsia, fatigue, pyrexia, urinary tract infection (What is urinary tract infection?). Nifedipine dosage: . During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), AXID (View Axid Review and Axid Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

6788853-3 | Hypertension
on Aug 01, 2008 Female patient from UNITED STATES , 56 years of age, was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: hypertension. Nifedipine dosage: .

6788752-7 | Constipation, Peripheral Coldness
Patient was taking Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), peripheral coldness on Apr 30, 2008 from UNITED STATES Additional patient health information: Male patient , 86 years of age, was diagnosed with peripheral coldness, peripheral vascular disorder and. Nifedipine dosage: .

6788732-1 | Neuropathy Peripheral, Oedema Peripheral
Adverse event was reported on Jun 05, 2008 by a Male patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 84 years of age, Patient had the following side effects: neuropathy peripheral, oedema peripheral. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), VITACAL (View Vitacal Review and Vitacal Label ), TRUSOPT (View Trusopt Review and Trusopt Label ), PILOCARPINE NITRATE (View Pilocarpine Nitrate Review and Pilocarpine Nitrate Label ).

6788581-4 | Oedema Peripheral, Rash
on May 02, 2008 Male patient from UNITED STATES , 63 years of age, weighting 321.0 lb, was diagnosed with hypertension, acne (What is acne?) and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: oedema peripheral, rash (What is rash?). Nifedipine dosage: . During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), DOXAZOSIN MESYLATE (View Doxazosin Mesylate Review and Doxazosin Mesylate Label ).

6788306-2 | Headache, Migraine, Paraesthesia
on Feb 01, 2009 Female patient from UNITED STATES , 65 years of age, weighting 131.0 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: headache (What is headache?), migraine (What is migraine?), paraesthesia. Nifedipine dosage: Qd. During the same period patient was treated with COREG (Bid) (View Coreg Review and Coreg Label ), VALSARTAN (Qd) (View Valsartan Review and Valsartan Label ), ASPIRIN (Qd) (View Aspirin Review and Aspirin Label ), ALPRAZOLAM (Prn) (View Alprazolam Review and Alprazolam Label ). Patient was hospitalized.

6767072-0 | Dizziness, Dyspnoea, Heart Rate Irregular, Palpitations
Patient was taking Nifedipine (View Usage). Patient had the following side effects: dizziness (What is dizziness?), dyspnoea, heart rate irregular, palpitations on May 31, 2010 from CANADA Additional patient health information: Female patient , 61 years of age, weighting 148.0 lb, was diagnosed with blood pressure increased and. Nifedipine dosage: 60mg. During the same period patient was treated with APO INDAPAMIDE (View Apo-indapamide Review and Apo-indapamide Label ), ACCUPRIL (View Accupril Review and Accupril Label ), APO ATENOLOL (View Apo-atenolol Review and Apo-atenolol Label ), DETROL LA (View Detrol La Review and Detrol La Label ), THYROID TAB (View Thyroid Tab Review and Thyroid Tab Label ), ROCALTROL (View Rocaltrol Review and Rocaltrol Label ).

6710552-4 | Caesarean Section, Clonus, Eclampsia, Headache, Hyperreflexia, Hypotension, Proteinuria, Visual Impairment
Adverse event was reported on Mar 11, 2010 by a Female patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with pregnancy induced hypertension and. Location: UNITED KINGDOM , 37 years of age, After Nifedipine was administered, patient had the following side effects: caesarean section, clonus, eclampsia, headache (What is headache?), hyperreflexia, hypotension, proteinuria, visual impairment. Patient was hospitalized.

6710551-2 | Aphasia, Myoclonus
on Mar 08, 2010 Male patient from UNITED KINGDOM , 51 years of age, weighting 154.3 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), myoclonus. Nifedipine dosage: . During the same period patient was treated with CEPHALEXIN (View Cephalexin Review and Cephalexin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ).

6710360-4 | International Normalised Ratio Increased, Post Procedural Haemorrhage, Tooth Disorder
on Apr 22, 2010 Male patient from UNITED KINGDOM , 48 years of age, was diagnosed with peripheral coldness and was treated with Nifedipine (View Usage). Patient had the following side effects: international normalised ratio increased, post procedural haemorrhage, tooth disorder (What is tooth disorder?). Nifedipine dosage: 5 Mg; Tid; Po. During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ).

6700142-1 | Hypertensive Crisis
Patient was taking Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: hypertensive crisis on Apr 13, 2010 from SPAIN Additional patient health information: Female patient , 69 years of age, . Nifedipine dosage: . During the same period patient was treated with PIPERACILLIN W/ (View Piperacillin W/ Review and Piperacillin W/ Label ), TAZOBACTAM (View Tazobactam Review and Tazobactam Label ), DOXAZOSIN (View Doxazosin Review and Doxazosin Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), HEPARIN (View Heparin Review and Heparin Label ). Patient was hospitalized.

6646242-6 | Malaise
Adverse event was reported on Mar 11, 2010 by a Female patient taking Nifedipine (View Usage) (Dosage: 60 Mg, 1x/day) was diagnosed with hypertension, cardiac disorder and. Location: UNITED STATES , weighting 127.9 lb, Patient experienced the following unwanted or unexpected effects: malaise. During the same period patient was treated with SYNTHROID (Unk, Daily) (View Synthroid Review and Synthroid Label ).

6635872-3 | Aphasia, Myoclonus
on Mar 08, 2010 Male patient from UNITED KINGDOM , 51 years of age, weighting 154.3 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient had the following side effects: aphasia (What is aphasia?), myoclonus. Nifedipine dosage: .

6621521-7 | Caesarean Section, Clonus, Headache, Hyperreflexia, Hypotension, Proteinuria, Visual Impairment
on Feb 12, 2010 Female patient from UNITED KINGDOM , 37 years of age, was diagnosed with pregnancy induced hypertension and was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: caesarean section, clonus, headache (What is headache?), hyperreflexia, hypotension, proteinuria, visual impairment. Nifedipine dosage: .

6621519-9 | Hypotension, Tachycardia
Patient was taking Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension, tachycardia on Feb 01, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 26 years of age, weighting 110.2 lb, was diagnosed with hypertension, convulsion, agitation, urine output decreased, caesarean section and. Nifedipine dosage: . During the same period patient was treated with PHENOBARBITAL (View Phenobarbital Review and Phenobarbital Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), CHLORPROMAZINE (View Chlorpromazine Review and Chlorpromazine Label ), MANNITOL (View Mannitol Review and Mannitol Label ), FRUSEMIDE (Two Doses) (View Frusemide Review and Frusemide Label ), PLASMANATE CUTTER (View Plasmanate Cutter Review and Plasmanate Cutter Label ), FROZEN HUMAN PLASMA (View Frozen Human Plasma Review and Frozen Human Plasma Label ), RINGER'S (View Ringer's Review and Ringer's Label ).

6617144-6 | Eosinophilic Pneumonia, Sjogren's Syndrome
Adverse event was reported on Aug 15, 2008 by a Female patient taking Nifedipine (View Usage) (Dosage: ) was diagnosed with hypertension, pneumonia bacterial and. Location: JAPAN , 54 years of age, Patient had the following side effects: eosinophilic pneumonia, sjogren's syndrome (What is sjogren's syndrome?). During the same period patient was treated with ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ).

6614750-X | Cardio-respiratory Arrest
on Feb 19, 2010 Female patient from UNITED STATES , 38 years of age, was treated with Nifedipine (View Usage). After Nifedipine was administered, patient had the following side effects: cardio-respiratory arrest. Nifedipine dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), QUINAPRIL HYDROCHLORIDE (View Quinapril Hydrochloride Review and Quinapril Hydrochloride Label ), SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ).

6611892-X | Headache, Hypertension, Product Substitution Issue
on Feb 26, 2010 Female patient from UNITED STATES , 64 years of age, weighting 148.3 lb, was diagnosed with hypertension and was treated with Nifedipine (View Usage). Patient experienced the following unwanted or unexpected effects: headache (What is headache?), hypertension, product substitution issue. Nifedipine dosage: 90mg Once Daily Po.

6604979-9 | Foetal Distress Syndrome, Premature Baby, Tachycardia Foetal
Patient was taking Nifedipine (View Usage). Patient had the following side effects: foetal distress syndrome, premature baby, tachycardia foetal on Feb 12, 2010 from UNITED KINGDOM Additional patient health information: Female patient , weighting 3.42 lb, was diagnosed with pregnancy induced hypertension and. Nifedipine dosage: Mother Took 10 Mg Capsule Sublingual.

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Nifedipine Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

Pat McGee   Location unknown

5:37pm on Wednesday, November 12th, 2008

The only potential side effect that coincides with my being prescribed Nifedipine is weight loss. Th... read more »

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Nifedipine 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 Nifedipine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Nifedipine 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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Nifedipine Reactions
Asthenia
Blood Creatinine Increased
Blood Pressure Decreased
Blood Pressure Inadequately Controlled
Blood Pressure Increased
Bradycardia
Caesarean Section
Cardiac ArrestWhat is Cardiac arrest?
Chest PainWhat is Chest pain?
Completed Suicide
Condition Aggravated
Cyanosis
DizzinessWhat is Dizziness?
Dyspnoea
Fatigue
Flushing
HeadacheWhat is Headache?
Heart Rate Increased
Hypertension
Hypotension
Intra-uterine Death
Malaise
NauseaWhat is Nausea?
Oedema Peripheral
Palpitations
Premature Baby
Renal Failure
Respiratory Arrest
Tachycardia
Vomiting
Nifedipine 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 Nifedipine 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!