Please choose an event type to view the corresponding MedsFacts report:

DRUG DEPENDENCE ( 351 FDA reports)
DENTAL CARIES ( 338 FDA reports)
PAIN ( 274 FDA reports)
DRUG PRESCRIBING ERROR ( 256 FDA reports)
NAUSEA ( 222 FDA reports)
DEPRESSION ( 221 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 218 FDA reports)
OVERDOSE ( 204 FDA reports)
ANXIETY ( 192 FDA reports)
SOMNOLENCE ( 183 FDA reports)
TOOTH LOSS ( 178 FDA reports)
VOMITING ( 169 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 143 FDA reports)
DIARRHOEA ( 137 FDA reports)
OFF LABEL USE ( 127 FDA reports)
DYSPNOEA ( 115 FDA reports)
DRUG INEFFECTIVE ( 114 FDA reports)
FATIGUE ( 110 FDA reports)
HYPERHIDROSIS ( 110 FDA reports)
BACK PAIN ( 106 FDA reports)
FALL ( 103 FDA reports)
SUICIDAL IDEATION ( 103 FDA reports)
TREMOR ( 103 FDA reports)
CONSTIPATION ( 102 FDA reports)
INSOMNIA ( 101 FDA reports)
SEDATION ( 100 FDA reports)
PYREXIA ( 97 FDA reports)
DRUG TOXICITY ( 90 FDA reports)
PNEUMONIA ( 81 FDA reports)
DEATH ( 80 FDA reports)
WEIGHT DECREASED ( 80 FDA reports)
MEMORY IMPAIRMENT ( 77 FDA reports)
DEPENDENCE ( 76 FDA reports)
MEDICATION ERROR ( 75 FDA reports)
LETHARGY ( 74 FDA reports)
LOSS OF CONSCIOUSNESS ( 74 FDA reports)
WITHDRAWAL SYNDROME ( 74 FDA reports)
TOOTH FRACTURE ( 71 FDA reports)
HEADACHE ( 70 FDA reports)
CONVULSION ( 69 FDA reports)
TOOTH DISORDER ( 69 FDA reports)
ARTHRALGIA ( 68 FDA reports)
ASTHENIA ( 68 FDA reports)
HYPERTENSION ( 68 FDA reports)
TOOTHACHE ( 68 FDA reports)
ANAEMIA ( 67 FDA reports)
MALAISE ( 67 FDA reports)
BONE DISORDER ( 65 FDA reports)
INFECTION ( 65 FDA reports)
VISION BLURRED ( 65 FDA reports)
ANGER ( 64 FDA reports)
TOOTH EXTRACTION ( 64 FDA reports)
ABDOMINAL PAIN ( 59 FDA reports)
DRUG ABUSE ( 58 FDA reports)
OSTEOARTHRITIS ( 58 FDA reports)
DIZZINESS ( 55 FDA reports)
PLEURAL EFFUSION ( 55 FDA reports)
TOOTH ABSCESS ( 55 FDA reports)
OSTEONECROSIS ( 53 FDA reports)
PAIN IN EXTREMITY ( 53 FDA reports)
CONFUSIONAL STATE ( 52 FDA reports)
INTENTIONAL DRUG MISUSE ( 52 FDA reports)
CARDIAC ARREST ( 51 FDA reports)
IMPAIRED HEALING ( 51 FDA reports)
ACCIDENTAL EXPOSURE ( 50 FDA reports)
HYPOTENSION ( 50 FDA reports)
OEDEMA PERIPHERAL ( 50 FDA reports)
GAIT DISTURBANCE ( 49 FDA reports)
MENTAL STATUS CHANGES ( 48 FDA reports)
INJURY ( 47 FDA reports)
OSTEOMYELITIS ( 47 FDA reports)
BALANCE DISORDER ( 45 FDA reports)
PAIN IN JAW ( 45 FDA reports)
ABNORMAL BEHAVIOUR ( 44 FDA reports)
ANHEDONIA ( 44 FDA reports)
CHEST PAIN ( 44 FDA reports)
DYSARTHRIA ( 44 FDA reports)
HALLUCINATION ( 44 FDA reports)
MUSCLE SPASMS ( 44 FDA reports)
OSTEONECROSIS OF JAW ( 44 FDA reports)
PARANOIA ( 44 FDA reports)
COMA ( 43 FDA reports)
DISEASE PROGRESSION ( 43 FDA reports)
EMPHYSEMA ( 43 FDA reports)
HYPOKALAEMIA ( 43 FDA reports)
RENAL FAILURE ( 43 FDA reports)
INFLAMMATION ( 42 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 41 FDA reports)
DEEP VEIN THROMBOSIS ( 41 FDA reports)
DEHYDRATION ( 41 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 41 FDA reports)
SLEEP DISORDER ( 41 FDA reports)
SUBSTANCE ABUSE ( 41 FDA reports)
ACCIDENTAL OVERDOSE ( 40 FDA reports)
BLOOD CREATININE INCREASED ( 40 FDA reports)
DRY MOUTH ( 40 FDA reports)
URINARY TRACT INFECTION ( 40 FDA reports)
HYPOAESTHESIA ( 38 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 38 FDA reports)
METASTASES TO BONE ( 38 FDA reports)
NEOPLASM MALIGNANT ( 38 FDA reports)
EMOTIONAL DISTRESS ( 37 FDA reports)
SINUS TACHYCARDIA ( 37 FDA reports)
AMNESIA ( 36 FDA reports)
BONE PAIN ( 36 FDA reports)
FUNGAL INFECTION ( 36 FDA reports)
MYOCARDIAL INFARCTION ( 36 FDA reports)
PANIC ATTACK ( 36 FDA reports)
PULMONARY EMBOLISM ( 36 FDA reports)
BRONCHITIS ( 35 FDA reports)
METASTATIC NEOPLASM ( 35 FDA reports)
ARACHNOIDITIS ( 34 FDA reports)
CELLULITIS ( 34 FDA reports)
COGNITIVE DISORDER ( 34 FDA reports)
DRUG INTERACTION ( 34 FDA reports)
INCORRECT DOSE ADMINISTERED ( 34 FDA reports)
PULMONARY OEDEMA ( 34 FDA reports)
SACROILIITIS ( 34 FDA reports)
SUICIDE ATTEMPT ( 34 FDA reports)
HAEMATOMA ( 33 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 33 FDA reports)
SWELLING ( 33 FDA reports)
DIABETES MELLITUS ( 32 FDA reports)
EATING DISORDER ( 32 FDA reports)
INADEQUATE ANALGESIA ( 32 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 32 FDA reports)
BONE DEBRIDEMENT ( 31 FDA reports)
CONDITION AGGRAVATED ( 31 FDA reports)
DECREASED APPETITE ( 31 FDA reports)
DYSGEUSIA ( 31 FDA reports)
FEELING ABNORMAL ( 31 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 31 FDA reports)
EXOSTOSIS ( 30 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 30 FDA reports)
THROMBOSIS ( 30 FDA reports)
TREATMENT NONCOMPLIANCE ( 30 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 29 FDA reports)
HALLUCINATION, AUDITORY ( 29 FDA reports)
RESPIRATORY DEPRESSION ( 29 FDA reports)
SLEEP APNOEA SYNDROME ( 28 FDA reports)
SWELLING FACE ( 28 FDA reports)
WEIGHT INCREASED ( 28 FDA reports)
ATAXIA ( 27 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 27 FDA reports)
CEREBRAL ATROPHY ( 27 FDA reports)
CEREBROVASCULAR ACCIDENT ( 27 FDA reports)
CHILLS ( 27 FDA reports)
ENDODONTIC PROCEDURE ( 27 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 27 FDA reports)
PERSONALITY CHANGE ( 27 FDA reports)
POOR PERSONAL HYGIENE ( 27 FDA reports)
ATELECTASIS ( 26 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 26 FDA reports)
DELIRIUM ( 26 FDA reports)
DRUG EFFECT DECREASED ( 26 FDA reports)
FAECAL INCONTINENCE ( 26 FDA reports)
FORMICATION ( 26 FDA reports)
HERNIA REPAIR ( 26 FDA reports)
MUSCULAR WEAKNESS ( 26 FDA reports)
PALPITATIONS ( 26 FDA reports)
THINKING ABNORMAL ( 26 FDA reports)
DENTAL OPERATION ( 25 FDA reports)
DISCOMFORT ( 25 FDA reports)
DRUG TOLERANCE ( 25 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 25 FDA reports)
EUPHORIC MOOD ( 25 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 25 FDA reports)
ORAL DISORDER ( 25 FDA reports)
PRURITUS ( 25 FDA reports)
THORACOTOMY ( 25 FDA reports)
VASCULAR OPERATION ( 25 FDA reports)
ACTINOMYCOSIS ( 24 FDA reports)
ALVEOLAR OSTEITIS ( 24 FDA reports)
ANOREXIA ( 24 FDA reports)
BREATH ODOUR ( 24 FDA reports)
DRUG ABUSER ( 24 FDA reports)
NEURALGIA ( 24 FDA reports)
PERIODONTAL OPERATION ( 24 FDA reports)
SINUS DISORDER ( 24 FDA reports)
TACHYCARDIA ( 24 FDA reports)
ASPIRATION PLEURAL CAVITY ( 23 FDA reports)
BURNING SENSATION ( 23 FDA reports)
DIPLOPIA ( 23 FDA reports)
HYPOXIA ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
SUBCUTANEOUS ABSCESS ( 23 FDA reports)
VENA CAVA FILTER INSERTION ( 23 FDA reports)
WHEELCHAIR USER ( 23 FDA reports)
ARTERIOSCLEROSIS ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
CONTUSION ( 22 FDA reports)
DISTURBANCE IN ATTENTION ( 22 FDA reports)
INCISIONAL DRAINAGE ( 22 FDA reports)
NERVOUSNESS ( 22 FDA reports)
NEUTROPENIA ( 22 FDA reports)
ORAL PAIN ( 22 FDA reports)
PURULENCE ( 22 FDA reports)
SINUSITIS ( 22 FDA reports)
AGITATION ( 21 FDA reports)
ARTHROPATHY ( 21 FDA reports)
GASTRITIS ( 21 FDA reports)
HEART RATE INCREASED ( 21 FDA reports)
HYPERSOMNIA ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
NEPHROLITHIASIS ( 21 FDA reports)
RECTAL HAEMORRHAGE ( 21 FDA reports)
STOMATITIS ( 21 FDA reports)
SYNCOPE ( 21 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 21 FDA reports)
TOOTH IMPACTED ( 21 FDA reports)
URINARY INCONTINENCE ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 20 FDA reports)
GRAND MAL CONVULSION ( 20 FDA reports)
HYPOPHAGIA ( 20 FDA reports)
LIVER CARCINOMA RUPTURED ( 20 FDA reports)
MAJOR DEPRESSION ( 20 FDA reports)
NECK PAIN ( 20 FDA reports)
NEUROPATHY PERIPHERAL ( 20 FDA reports)
OSTEOPENIA ( 20 FDA reports)
THROMBOPHLEBITIS ( 20 FDA reports)
CATARACT ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
DEAFNESS ( 19 FDA reports)
DECREASED ACTIVITY ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
EPIDURAL LIPOMATOSIS ( 19 FDA reports)
EXERCISE TOLERANCE DECREASED ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
HAEMATURIA ( 19 FDA reports)
INTESTINAL OBSTRUCTION ( 19 FDA reports)
LIFE EXPECTANCY SHORTENED ( 19 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 19 FDA reports)
RHINORRHOEA ( 19 FDA reports)
ROAD TRAFFIC ACCIDENT ( 19 FDA reports)
ARTHRITIS ( 18 FDA reports)
BONE LESION ( 18 FDA reports)
DEVICE FAILURE ( 18 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 18 FDA reports)
PHYSICAL DISABILITY ( 18 FDA reports)
SEXUAL DYSFUNCTION ( 18 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 18 FDA reports)
ABDOMINAL PAIN LOWER ( 17 FDA reports)
BEDRIDDEN ( 17 FDA reports)
BIPOLAR I DISORDER ( 17 FDA reports)
COUGH ( 17 FDA reports)
DYSTHYMIC DISORDER ( 17 FDA reports)
DYSURIA ( 17 FDA reports)
MIGRAINE ( 17 FDA reports)
MULTIPLE MYELOMA ( 17 FDA reports)
MYELITIS TRANSVERSE ( 17 FDA reports)
POST LAMINECTOMY SYNDROME ( 17 FDA reports)
RESPIRATORY ARREST ( 17 FDA reports)
SKIN LACERATION ( 17 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 17 FDA reports)
TOOTH DECALCIFICATION ( 17 FDA reports)
UNEVALUABLE EVENT ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
BREATH SOUNDS ABNORMAL ( 16 FDA reports)
CARDIAC DISORDER ( 16 FDA reports)
DEVICE LEAKAGE ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
ERECTILE DYSFUNCTION ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
HAEMATOCHEZIA ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
JOINT SWELLING ( 16 FDA reports)
LUNG OPERATION ( 16 FDA reports)
MASTICATION DISORDER ( 16 FDA reports)
MUSCULOSKELETAL PAIN ( 16 FDA reports)
PLEURAL FIBROSIS ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
SKIN LESION ( 16 FDA reports)
SPINAL CORD DISORDER ( 16 FDA reports)
BREAST CANCER METASTATIC ( 15 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 15 FDA reports)
DRUG SCREEN POSITIVE ( 15 FDA reports)
EPISTAXIS ( 15 FDA reports)
INCONTINENCE ( 15 FDA reports)
MUCOSAL INFLAMMATION ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 15 FDA reports)
NYSTAGMUS ( 15 FDA reports)
OVARIAN CYST ( 15 FDA reports)
PERICARDIAL EFFUSION ( 15 FDA reports)
RASH ( 15 FDA reports)
SCREAMING ( 15 FDA reports)
SPINAL OSTEOARTHRITIS ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
TOOTH INFECTION ( 15 FDA reports)
ANGIOPATHY ( 14 FDA reports)
BURSITIS ( 14 FDA reports)
DENTURE WEARER ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
ELECTROLYTE IMBALANCE ( 14 FDA reports)
HIATUS HERNIA ( 14 FDA reports)
HYDRONEPHROSIS ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
MALNUTRITION ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
OSTEOPETROSIS ( 14 FDA reports)
OXYGEN SATURATION DECREASED ( 14 FDA reports)
PELVIC PAIN ( 14 FDA reports)
RADIOTHERAPY ( 14 FDA reports)
RASH PRURITIC ( 14 FDA reports)
STAPHYLOCOCCAL INFECTION ( 14 FDA reports)
TENDERNESS ( 14 FDA reports)
UNRESPONSIVE TO STIMULI ( 14 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 13 FDA reports)
AGGRESSION ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
COLITIS ( 13 FDA reports)
FAILURE TO THRIVE ( 13 FDA reports)
HEPATIC STEATOSIS ( 13 FDA reports)
IMPAIRED DRIVING ABILITY ( 13 FDA reports)
LUMBAR SPINAL STENOSIS ( 13 FDA reports)
MASS ( 13 FDA reports)
MOOD ALTERED ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE ( 13 FDA reports)
MULTIPLE SCLEROSIS ( 13 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 13 FDA reports)
OEDEMA ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
SCIATICA ( 13 FDA reports)
SELF-MEDICATION ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SPINAL COMPRESSION FRACTURE ( 13 FDA reports)
SPONDYLITIS ( 13 FDA reports)
AGEUSIA ( 12 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 12 FDA reports)
AXILLARY MASS ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
CHEST DISCOMFORT ( 12 FDA reports)
CRYING ( 12 FDA reports)
CYST ( 12 FDA reports)
DIALYSIS ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
LUNG INFILTRATION ( 12 FDA reports)
MENTAL DISORDER ( 12 FDA reports)
MENTAL IMPAIRMENT ( 12 FDA reports)
MOBILITY DECREASED ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
NIGHT SWEATS ( 12 FDA reports)
OSTEOPOROSIS ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PARTNER STRESS ( 12 FDA reports)
POST PROCEDURAL COMPLICATION ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
RESPIRATORY RATE INCREASED ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
SUICIDAL BEHAVIOUR ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
BACK INJURY ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
CARDIOMEGALY ( 11 FDA reports)
CAUDA EQUINA SYNDROME ( 11 FDA reports)
DECREASED INTEREST ( 11 FDA reports)
DENTAL IMPLANTATION ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
ILEUS ( 11 FDA reports)
INGUINAL HERNIA ( 11 FDA reports)
LACERATION ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
OVARIAN MASS ( 11 FDA reports)
POLYURIA ( 11 FDA reports)
RADICULOPATHY ( 11 FDA reports)
SOFT TISSUE DISORDER ( 11 FDA reports)
SPEECH DISORDER ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 10 FDA reports)
COLONIC OBSTRUCTION ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
ECONOMIC PROBLEM ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
HOT FLUSH ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
MEGACOLON ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PARAPLEGIA ( 10 FDA reports)
PLASMACYTOMA ( 10 FDA reports)
PULMONARY HAEMORRHAGE ( 10 FDA reports)
RENAL CYST ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
RESPIRATORY RATE DECREASED ( 10 FDA reports)
RETINOPATHY ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
SPINAL CORPECTOMY ( 10 FDA reports)
STUPOR ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
THORACIC OPERATION ( 10 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ABSCESS ORAL ( 9 FDA reports)
APPLICATION SITE RASH ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
BRUXISM ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
COLONIC STENOSIS ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
DROP ATTACKS ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
EXPOSED BONE IN JAW ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
FACET JOINT SYNDROME ( 9 FDA reports)
FOOT FRACTURE ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
GINGIVAL INFECTION ( 9 FDA reports)
GINGIVAL PAIN ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
IMPRISONMENT ( 9 FDA reports)
JOINT INJURY ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
NEUTROPHIL COUNT DECREASED ( 9 FDA reports)
ORAL SURGERY ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PERINEURIAL CYST ( 9 FDA reports)
PROSTATE CANCER ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
SCOLIOSIS ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 9 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 9 FDA reports)
APPLICATION SITE ERYTHEMA ( 8 FDA reports)
APPLICATION SITE IRRITATION ( 8 FDA reports)
ASCITES ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BULIMIA NERVOSA ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DETOXIFICATION ( 8 FDA reports)
DILATATION VENTRICULAR ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DRUG DISPENSING ERROR ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FEAR ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
GASTRIC DISORDER ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GINGIVAL RECESSION ( 8 FDA reports)
GLAUCOMA ( 8 FDA reports)
HAEMODYNAMIC INSTABILITY ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
INCOHERENT ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PNEUMATOSIS INTESTINALIS ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
PULSE ABSENT ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
TOOTH DISCOLOURATION ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
ALCOHOL USE ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
COLOSTOMY ( 7 FDA reports)
COORDINATION ABNORMAL ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
DRUG DIVERSION ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
GASTROINTESTINAL PAIN ( 7 FDA reports)
GINGIVAL BLEEDING ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
LACRIMATION INCREASED ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
MAXILLOFACIAL OPERATION ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
METASTASES TO LIVER ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
ORTHOSIS USER ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PLEURISY ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
PURULENT DISCHARGE ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
SNORING ( 7 FDA reports)
SURGERY ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
ANDROGEN DEFICIENCY ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
ARTERIAL BYPASS OPERATION ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLADDER PROLAPSE ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 6 FDA reports)
ETHMOID SINUS SURGERY ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FEELING HOT AND COLD ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
FRUSTRATION ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
MENINGIOMA ( 6 FDA reports)
METASTASES TO MUSCLE ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NASAL SEPTUM DEVIATION ( 6 FDA reports)
NASAL SEPTUM PERFORATION ( 6 FDA reports)
NECK INJURY ( 6 FDA reports)
NERVE BLOCK ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PLASMAPHERESIS ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
PROLAPSE REPAIR ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
SARCOIDOSIS ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 6 FDA reports)
STRESS ( 6 FDA reports)
TACHYARRHYTHMIA ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
URETHRAL PAIN ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
ACCIDENTAL DEATH ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
APNOEA ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FASCIITIS ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
OPIATES POSITIVE ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VICTIM OF SEXUAL ABUSE ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APPLICATION SITE PRURITUS ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
FACE AND MOUTH X-RAY ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NO ADVERSE EFFECT ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
VISCERAL CONGESTION ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ADMINISTRATION SITE REACTION ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
CARDIOTOXICITY ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GINGIVAL BLISTER ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
IUD MIGRATION ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LEGAL PROBLEM ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO PANCREAS ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
POST PROCEDURAL SWELLING ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRODUCT PACKAGING ISSUE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RETINAL TEAR ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SCAR ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENNOX-GASTAUT SYNDROME ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC NERVE NEOPLASM ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT FRIABLE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
STARING ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR OPERATION ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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