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)
Flatulence07.01.04.002--
Flushing24.03.01.002; 23.06.05.003; 08.01.03.0250.000634%
Foetal distress syndrome18.03.02.0030.000261%Not Available
Food interaction08.06.03.002--Not Available
Gait disturbance15.03.05.013; 17.02.05.016; 08.01.02.002--
Gamma-glutamyltransferase increased13.03.04.024--
Gastric cancer16.13.03.001; 07.21.02.0010.000075%Not Available
Gastric haemorrhage24.07.02.007; 07.12.01.0010.000075%
Gastrooesophageal reflux disease07.02.02.0030.000075%
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal haemorrhage24.07.02.009; 07.12.02.001--Not Available
Gastrointestinal pain07.01.05.005--
Gingival bleeding24.07.02.010; 07.09.07.0010.000112%Not Available
Gingival disorder07.09.13.004--Not Available
Gingival hypertrophy07.09.13.0080.000515%Not Available
Gingival swelling07.09.13.0130.000276%Not Available
Gingivitis07.09.10.002; 11.01.04.013--
Gout15.01.06.001; 14.09.01.001--Not Available
Gynaecomastia21.05.04.003; 05.05.02.003--
Haematuria21.10.01.018; 24.07.01.047; 20.02.01.006--
Haemoglobin13.01.05.018--Not Available
Haemolytic anaemia01.06.03.002--Not Available
Hallucination, visual19.10.04.0070.000075%Not Available
Head discomfort17.02.05.0270.000201%Not Available
Headache17.14.01.0010.002590%
Hepatitis09.01.07.0040.000164%Not Available
Hyperglycaemia14.06.02.002; 05.06.02.0020.000149%
Hyperhidrosis08.01.03.028; 23.02.03.004--
Hyperkalaemia14.05.03.0010.000112%
Hyperkinesia17.01.02.008--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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