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

PAIN ( 119 FDA reports)
DYSPNOEA ( 100 FDA reports)
ANXIETY ( 94 FDA reports)
CHEST PAIN ( 90 FDA reports)
FATIGUE ( 82 FDA reports)
NAUSEA ( 79 FDA reports)
ABDOMINAL PAIN ( 75 FDA reports)
DIZZINESS ( 75 FDA reports)
ABDOMINAL PAIN UPPER ( 69 FDA reports)
DEPRESSION ( 67 FDA reports)
DRUG INEFFECTIVE ( 65 FDA reports)
HEADACHE ( 63 FDA reports)
ARTHRALGIA ( 61 FDA reports)
CHOLELITHIASIS ( 61 FDA reports)
ASTHENIA ( 58 FDA reports)
ANAEMIA ( 56 FDA reports)
INJURY ( 55 FDA reports)
CHOLECYSTITIS CHRONIC ( 52 FDA reports)
DIARRHOEA ( 52 FDA reports)
VOMITING ( 52 FDA reports)
INSOMNIA ( 51 FDA reports)
CHEST DISCOMFORT ( 46 FDA reports)
BACK PAIN ( 45 FDA reports)
HYPOTENSION ( 45 FDA reports)
MALAISE ( 45 FDA reports)
PULMONARY EMBOLISM ( 44 FDA reports)
PAIN IN EXTREMITY ( 42 FDA reports)
HYPERSENSITIVITY ( 39 FDA reports)
RASH ( 39 FDA reports)
WEIGHT DECREASED ( 37 FDA reports)
CONSTIPATION ( 36 FDA reports)
DEEP VEIN THROMBOSIS ( 36 FDA reports)
HYPOAESTHESIA ( 36 FDA reports)
PALPITATIONS ( 35 FDA reports)
ERYTHEMA ( 34 FDA reports)
PRURITUS ( 34 FDA reports)
PYREXIA ( 33 FDA reports)
DECREASED APPETITE ( 32 FDA reports)
DEHYDRATION ( 32 FDA reports)
COUGH ( 31 FDA reports)
GALLBLADDER DISORDER ( 31 FDA reports)
OVERDOSE ( 31 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 30 FDA reports)
PARAESTHESIA ( 30 FDA reports)
FLUSHING ( 28 FDA reports)
HYPERHIDROSIS ( 28 FDA reports)
MUSCLE SPASMS ( 28 FDA reports)
URINARY TRACT INFECTION ( 27 FDA reports)
MIGRAINE ( 26 FDA reports)
SOMNOLENCE ( 26 FDA reports)
DRUG INTERACTION ( 25 FDA reports)
FEELING ABNORMAL ( 25 FDA reports)
HYPERTENSION ( 25 FDA reports)
NECK PAIN ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
RECTAL HAEMORRHAGE ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
BRONCHITIS ( 24 FDA reports)
EMOTIONAL DISTRESS ( 24 FDA reports)
MUSCULOSKELETAL PAIN ( 24 FDA reports)
RESPIRATORY FAILURE ( 24 FDA reports)
SINUSITIS ( 24 FDA reports)
CONVULSION ( 23 FDA reports)
DRY MOUTH ( 23 FDA reports)
INCORRECT DOSE ADMINISTERED ( 23 FDA reports)
MYALGIA ( 23 FDA reports)
MYOCARDIAL INFARCTION ( 23 FDA reports)
PNEUMONIA ( 23 FDA reports)
TYPE 2 DIABETES MELLITUS ( 23 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 22 FDA reports)
BLOOD GLUCOSE INCREASED ( 22 FDA reports)
MUSCULAR WEAKNESS ( 22 FDA reports)
NEUROPATHY PERIPHERAL ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
SUICIDE ATTEMPT ( 22 FDA reports)
FIBROMYALGIA ( 21 FDA reports)
HYPERLIPIDAEMIA ( 21 FDA reports)
MEDICATION RESIDUE ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 20 FDA reports)
OSTEONECROSIS OF JAW ( 20 FDA reports)
TREMOR ( 20 FDA reports)
URTICARIA ( 20 FDA reports)
BILIARY DYSKINESIA ( 19 FDA reports)
CROHN'S DISEASE ( 19 FDA reports)
EXOSTOSIS ( 19 FDA reports)
LEUKOCYTOSIS ( 19 FDA reports)
OSTEONECROSIS ( 19 FDA reports)
TACHYCARDIA ( 19 FDA reports)
ANHEDONIA ( 18 FDA reports)
ATELECTASIS ( 18 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
CONTUSION ( 18 FDA reports)
EMOTIONAL DISORDER ( 18 FDA reports)
GASTROINTESTINAL DISORDER ( 18 FDA reports)
NERVOUSNESS ( 18 FDA reports)
PRODUCT QUALITY ISSUE ( 18 FDA reports)
STRESS ( 18 FDA reports)
SWELLING FACE ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
ARTHROPATHY ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
DYSURIA ( 17 FDA reports)
HYPOKALAEMIA ( 17 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 17 FDA reports)
POUCHITIS ( 17 FDA reports)
COLITIS ULCERATIVE ( 16 FDA reports)
DRY EYE ( 16 FDA reports)
DRY SKIN ( 16 FDA reports)
HAEMORRHOIDS ( 16 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 16 FDA reports)
PHARYNGEAL OEDEMA ( 16 FDA reports)
DEATH ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
FALL ( 15 FDA reports)
FEELING HOT ( 15 FDA reports)
HAEMATOCHEZIA ( 15 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
OSTEOARTHRITIS ( 15 FDA reports)
OSTEOMYELITIS ( 15 FDA reports)
TENDONITIS ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 15 FDA reports)
ABDOMINAL DISCOMFORT ( 14 FDA reports)
AMNESIA ( 14 FDA reports)
DISABILITY ( 14 FDA reports)
EYE PAIN ( 14 FDA reports)
FLATULENCE ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
LIP DRY ( 14 FDA reports)
METASTATIC NEOPLASM ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
SLEEP APNOEA SYNDROME ( 14 FDA reports)
SWOLLEN TONGUE ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
BURSITIS ( 13 FDA reports)
CHILLS ( 13 FDA reports)
CHOLECYSTITIS ACUTE ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
DYSPHAGIA ( 13 FDA reports)
FAECES DISCOLOURED ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
HEPATIC LESION ( 13 FDA reports)
INTESTINAL HAEMORRHAGE ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 13 FDA reports)
PERNICIOUS ANAEMIA ( 13 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
ACNE ( 12 FDA reports)
BREAST RECONSTRUCTION ( 12 FDA reports)
BURNING SENSATION ( 12 FDA reports)
CHOLECYSTITIS ( 12 FDA reports)
COLITIS ( 12 FDA reports)
ECZEMA ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
KIDNEY INFECTION ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
SKIN LACERATION ( 12 FDA reports)
THROMBOCYTOSIS ( 12 FDA reports)
THROMBOSIS ( 12 FDA reports)
TINNITUS ( 12 FDA reports)
TOOTH EXTRACTION ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
HOT FLUSH ( 11 FDA reports)
INJECTION SITE PAIN ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
PAIN OF SKIN ( 11 FDA reports)
PULMONARY FIBROSIS ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
SKIN LESION ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
WHEEZING ( 11 FDA reports)
ANOREXIA ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CERVICAL SPINAL STENOSIS ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
DRUG EFFECT DECREASED ( 10 FDA reports)
DYSPHONIA ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
HILAR LYMPHADENOPATHY ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
POLLAKIURIA ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ALOPECIA ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BREAST DISCHARGE ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
DEPRESSED MOOD ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HAND FRACTURE ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
MYCOSIS FUNGOIDES ( 9 FDA reports)
NEOPLASM MALIGNANT ( 9 FDA reports)
ORAL DISORDER ( 9 FDA reports)
OSTEOPENIA ( 9 FDA reports)
OTITIS EXTERNA ( 9 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
PYODERMA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
SLEEP DISORDER ( 9 FDA reports)
SPINAL OSTEOARTHRITIS ( 9 FDA reports)
THROMBOSIS IN DEVICE ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ACUTE STRESS DISORDER ( 8 FDA reports)
ANAL INFLAMMATION ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
CRYING ( 8 FDA reports)
CYST ( 8 FDA reports)
DERMAL CYST ( 8 FDA reports)
DIABETIC COMPLICATION ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
FLANK PAIN ( 8 FDA reports)
GALLBLADDER OPERATION ( 8 FDA reports)
GASTROENTERITIS VIRAL ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HYPERGLYCAEMIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 8 FDA reports)
JOINT SPRAIN ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
OBESITY ( 8 FDA reports)
OEDEMA MUCOSAL ( 8 FDA reports)
PARANASAL SINUS DISCOMFORT ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
RASH MACULAR ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
RESTLESS LEGS SYNDROME ( 8 FDA reports)
SARCOIDOSIS ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TOOTH FRACTURE ( 8 FDA reports)
VENOUS OCCLUSION ( 8 FDA reports)
VENOUS THROMBOSIS ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
VITAMIN B12 DEFICIENCY ( 8 FDA reports)
VULVOVAGINAL DRYNESS ( 8 FDA reports)
ANGER ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CATARACT ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
FEAR ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 7 FDA reports)
HISTOPLASMOSIS ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PELVIC PAIN ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
THINKING ABNORMAL ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
APHONIA ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 6 FDA reports)
ERYTHEMA NODOSUM ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FIBROSIS ( 6 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LIMB REDUCTION DEFECT ( 6 FDA reports)
LOW SET EARS ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
PULMONARY HYPOPLASIA ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
SCAR ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
CONJUNCTIVAL ABRASION ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 5 FDA reports)
EAR INFECTION ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
OSTEOLYSIS ( 5 FDA reports)
OTITIS MEDIA ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
POLYP ( 5 FDA reports)
PRESBYOPIA ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TOOTH DISORDER ( 5 FDA reports)
TOOTH INFECTION ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
WINGED SCAPULA ( 5 FDA reports)
ABSCESS ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CARTILAGE INJURY ( 4 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
COMPLICATION OF DELIVERY ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DIASTOLIC HYPERTENSION ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENDOMETRIAL ATROPHY ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
FOREIGN BODY REACTION ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFERTILITY ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MAMMARY DUCT ECTASIA ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MICROCYTIC ANAEMIA ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
SCAR EXCISION ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TRACHEAL OEDEMA ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADHESION ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOLIPIN ANTIBODY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
COMA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DERMOID CYST ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GINGIVAL DISORDER ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GINGIVAL OPERATION ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NODULE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POISONING ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PULMONARY VEIN OCCLUSION ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
TIC ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD AND NECK CANCER STAGE III ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY NEGATIVE ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY INDOLENT ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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