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

DRUG INEFFECTIVE ( 322 FDA reports)
DRUG EFFECT DECREASED ( 99 FDA reports)
NAUSEA ( 74 FDA reports)
DIZZINESS ( 62 FDA reports)
ANXIETY ( 59 FDA reports)
PAIN ( 53 FDA reports)
DYSPNOEA ( 49 FDA reports)
FATIGUE ( 49 FDA reports)
CONSTIPATION ( 44 FDA reports)
HYPERTENSION ( 44 FDA reports)
INSOMNIA ( 44 FDA reports)
OVERDOSE ( 41 FDA reports)
VOMITING ( 38 FDA reports)
OEDEMA PERIPHERAL ( 37 FDA reports)
SOMNOLENCE ( 37 FDA reports)
OSTEOPENIA ( 36 FDA reports)
PNEUMONIA ( 34 FDA reports)
CONDITION AGGRAVATED ( 33 FDA reports)
INJURY ( 33 FDA reports)
ASTHENIA ( 31 FDA reports)
COUGH ( 31 FDA reports)
DIARRHOEA ( 31 FDA reports)
BACK PAIN ( 30 FDA reports)
WEIGHT DECREASED ( 29 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
HEADACHE ( 27 FDA reports)
MALAISE ( 27 FDA reports)
SYNCOPE ( 27 FDA reports)
TREMOR ( 27 FDA reports)
DEEP VEIN THROMBOSIS ( 26 FDA reports)
DEPRESSION ( 26 FDA reports)
INFECTION ( 26 FDA reports)
PARAESTHESIA ( 26 FDA reports)
RHINORRHOEA ( 26 FDA reports)
ARTHRALGIA ( 25 FDA reports)
HEART RATE INCREASED ( 25 FDA reports)
OSTEONECROSIS OF JAW ( 25 FDA reports)
ABDOMINAL PAIN ( 24 FDA reports)
ANHEDONIA ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
FALL ( 24 FDA reports)
HYPERSENSITIVITY ( 24 FDA reports)
OSTEOARTHRITIS ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
ANAEMIA ( 23 FDA reports)
ATELECTASIS ( 23 FDA reports)
EYE PRURITUS ( 23 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 23 FDA reports)
MULTIPLE MYELOMA ( 23 FDA reports)
PATHOLOGICAL FRACTURE ( 23 FDA reports)
RENAL FAILURE CHRONIC ( 23 FDA reports)
BRONCHITIS ( 22 FDA reports)
CHEST PAIN ( 22 FDA reports)
FEELING ABNORMAL ( 22 FDA reports)
MUSCLE SPASMS ( 22 FDA reports)
MYALGIA ( 22 FDA reports)
NASAL CONGESTION ( 22 FDA reports)
DECREASED APPETITE ( 21 FDA reports)
PRURITUS ( 21 FDA reports)
URINARY TRACT INFECTION ( 21 FDA reports)
CORONARY ARTERY DISEASE ( 20 FDA reports)
DIABETES MELLITUS ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
HYPERCHOLESTEROLAEMIA ( 20 FDA reports)
HYPOAESTHESIA ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
NEURALGIA ( 20 FDA reports)
OBESITY ( 20 FDA reports)
SINUSITIS ( 20 FDA reports)
SLEEP DISORDER ( 20 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
EXOSTOSIS ( 19 FDA reports)
HYPERHIDROSIS ( 19 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 19 FDA reports)
PANCYTOPENIA ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
AGITATION ( 18 FDA reports)
DRY MOUTH ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
LACRIMATION INCREASED ( 18 FDA reports)
RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
SNEEZING ( 18 FDA reports)
SWELLING ( 18 FDA reports)
GOITRE ( 17 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 17 FDA reports)
MENTAL STATUS CHANGES ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
SINUS DISORDER ( 17 FDA reports)
SPINAL OSTEOARTHRITIS ( 17 FDA reports)
URINARY INCONTINENCE ( 17 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
BONE DISORDER ( 16 FDA reports)
BONE MARROW FAILURE ( 16 FDA reports)
BONE NEOPLASM ( 16 FDA reports)
CATARACT ( 16 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
COLITIS ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
FRACTURED SACRUM ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
HYPERLIPIDAEMIA ( 16 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 16 FDA reports)
HYPOTHYROIDISM ( 16 FDA reports)
OSTEOLYSIS ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 16 FDA reports)
PROTEINURIA ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
RASH ( 16 FDA reports)
RASH MACULO-PAPULAR ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
AORTIC CALCIFICATION ( 15 FDA reports)
DRUG INTERACTION ( 15 FDA reports)
HIATUS HERNIA ( 15 FDA reports)
HYPOVENTILATION ( 15 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 15 FDA reports)
PERICARDIAL EFFUSION ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
BREATH ODOUR ( 14 FDA reports)
CAROTID ARTERY STENOSIS ( 14 FDA reports)
CHEST DISCOMFORT ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
DIABETIC RETINOPATHY ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
GASTROINTESTINAL PAIN ( 14 FDA reports)
RHINITIS ALLERGIC ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
ACROCHORDON ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CELLULITIS ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
GROIN PAIN ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
RIB FRACTURE ( 12 FDA reports)
ALOPECIA ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
DEATH ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HAEMORRHOIDS ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
ADVERSE DRUG REACTION ( 10 FDA reports)
CHILLS ( 10 FDA reports)
DEFORMITY ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
IMPAIRED HEALING ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
DERMOID CYST ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
BONE DEFORMITY ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
MUSCLE TWITCHING ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
MUSCULOSKELETAL PAIN ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
REFLUX GASTRITIS ( 8 FDA reports)
SYNOVIAL CYST ( 8 FDA reports)
TOOTHACHE ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
CERVICAL SPINAL STENOSIS ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
FACET JOINT SYNDROME ( 7 FDA reports)
FEELING JITTERY ( 7 FDA reports)
GALLBLADDER DISORDER ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
LUMBAR SPINAL STENOSIS ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SLEEP APNOEA SYNDROME ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TABLET PHYSICAL ISSUE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
ANGIOPATHY ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG EFFECT DELAYED ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PYURIA ( 6 FDA reports)
STRESS ( 6 FDA reports)
TOOTH FRACTURE ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ACTINOMYCOSIS ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
EAR PRURITUS ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
NASAL DRYNESS ( 5 FDA reports)
NOCTURIA ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
LACERATION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MUCOSAL ATROPHY ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGER ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EXOMPHALOS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FOETAL MALPRESENTATION ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KYPHOSCOLIOSIS ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MASS ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORAL PAPILLOMA ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENTEROBIASIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS INJURY ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA AQUAGENIC ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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