Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Nifedipine
Drug ID BADD_D01566
Description Nifedipine, or BAY a 1040, is a first generation dihydropyridine L-type calcium channel blocker, similar to [nicardipine].[A190210,A190273,A175390,L11383] Nifedipine was developed by Bayer and first described in the literature, along with other dihydropyridines, in 1972.[A175390,A190276] Since nifedipine's development, second and third generation dihydropyridines have been developed with slower onsets and longer durations of action.[A190273] The most popular of the third generation dihydropyridines is [amlodipine].[A190273] Nifedipine was granted FDA approval on 31 December 1981.[L11383]
Indications and Usage Nifedipine capsules are indicated to treat vasospastic angina and chronic stable angina.[L11383] Extended release tablets are indicated to treat vasospastic angina, chronic stable angina, and hypertension.[L11389,L1245]
Marketing Status approved
ATC Code C08CA05
DrugBank ID DB01115
KEGG ID D00437
MeSH ID D009543
PubChem ID 4485
TTD Drug ID D04OSE
NDC Product Code 0904-7229; 46438-0635; 52932-0711; 0069-2670; 68981-039; 23155-194; 23155-195; 43826-031; 46708-732; 50090-1843; 50742-622; 51655-738; 55289-798; 62332-734; 68084-597; 68382-687; 68645-512; 68682-106; 70771-1365; 71335-0497; 48589-0006; 51927-0233; 0069-2660; 46708-734; 50742-261; 50742-262; 51407-624; 0228-2497; 60429-049; 62175-262; 62332-732; 68084-598; 70771-1192; 71610-055; 11014-0036; 11014-0341; 52133-0028; 60592-507; 50742-260; 59651-297; 68071-2619; 68382-688; 68645-603; 68682-108; 69315-211; 70771-1191; 70807-503; 71335-0744; 71335-1721; 71335-9651; 55154-4690; 68084-603; 70934-973; 11014-0035; 11014-0342; 48292-0034; 62991-1106; 43826-030; 46708-733; 50268-598; 50742-621; 51655-780; 55154-4157; 62175-261; 63629-9109; 68382-686; 68682-105; 70771-1366; 71610-689; 0904-7081; 0069-2650; 24979-009; 24979-011; 50268-599; 50742-620; 59651-295; 59651-296; 59762-1004; 67877-757; 68645-513; 68682-109; 71205-965; 71335-0489; 71610-290; 72162-1277; 38779-0280; 51927-5205; 65427-250; 71052-650; 51655-407; 51655-798; 60429-048; 62135-521; 67877-758; 68382-689; 70934-603; 71205-963; 71335-2132; 71610-144; 72214-503; 72789-219; 49452-4847; 52133-0009; 24979-010; 50268-597; 51655-386; 62135-523; 62175-260; 62332-733; 68382-685; 71205-412; 71335-1550; 71610-012; 0904-7082; 82920-709; 43826-032; 0228-2530; 53808-1118; 62135-522; 63187-875; 68682-107; 68788-7642; 68788-8164; 69315-212; 70518-2679; 70518-3520; 12527-0787; 0904-7208; 46438-0052; 60524-002; 50090-4158; 50090-5284; 50090-5328; 50090-6201; 50090-6450; 51655-990; 55154-8177; 67877-756; 68071-4411; 68382-690; 68645-604; 70771-1190; 70771-1367; 70934-963; 71205-964; 11014-0038; 51552-0720; 50090-4234; 50090-6203; 51407-622; 51407-623; 51655-593; 60429-047
UNII I9ZF7L6G2L
Synonyms Nifedipine | Bay-1040 | Bay 1040 | Bay1040 | BAY-a-1040 | BAY a 1040 | BAYa1040 | Cordipin | Cordipine | Corinfar | Korinfar | Nifangin | Nifedipine Monohydrochloride | Monohydrochloride, Nifedipine | Procardia | Procardia XL | Nifedipine-GTIS | Nifedipine GTIS | Vascard | Adalat | Fenigidin
Chemical Information
Molecular Formula C17H18N2O6
CAS Registry Number 21829-25-4
SMILES CC1=C(C(C(=C(N1)C)C(=O)OC)C2=CC=CC=C2[N+](=O)[O-])C(=O)OC
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Ataxia17.02.02.001; 08.01.02.004--
Atrial fibrillation02.03.03.002--
Atrioventricular block02.03.01.0020.000224%Not Available
Atrioventricular block complete02.03.01.0030.000075%
Back pain15.03.04.005--
Basal cell carcinoma23.08.02.001; 16.03.02.0010.000075%Not Available
Bezoar07.11.01.0080.000075%Not Available
Blindness17.17.01.003; 06.02.10.0030.000224%Not Available
Blindness transient06.02.10.006; 17.17.01.004--Not Available
Blindness unilateral06.02.10.007; 17.17.01.016--Not Available
Blister23.03.01.001; 12.01.06.002--Not Available
Blood pressure fluctuation24.06.01.0020.000254%Not Available
Blood pressure increased13.14.03.005--Not Available
Body temperature increased13.15.01.001--Not Available
Bradycardia02.03.02.0020.000799%Not Available
Bradycardia foetal18.03.02.006; 02.03.02.0180.000187%Not Available
Breast engorgement21.05.05.002; 18.08.02.001--Not Available
Breast pain21.05.05.003--
Bronchiectasis22.03.02.0050.000075%Not Available
Bronchospasm22.03.01.004; 10.01.03.012--
Bundle branch block left02.03.01.0070.000112%Not Available
Burning sensation08.01.09.029; 17.02.06.0010.000291%Not Available
Cardiac arrest02.03.04.0010.001306%
Cardiac failure02.05.01.0010.000149%
Cardiac failure congestive02.05.01.0020.000224%Not Available
Cardio-respiratory arrest22.02.06.007; 02.03.04.0020.000336%Not Available
Cardiogenic shock02.05.01.003; 24.06.02.0060.000373%Not Available
Cardiovascular disorder02.11.01.010; 24.03.02.009--Not Available
Cataract06.06.01.001--
Cellulitis23.11.02.004; 11.02.01.001--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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