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

NO ADVERSE EVENT ( 4164 FDA reports)
DRUG INEFFECTIVE ( 1929 FDA reports)
HEADACHE ( 1871 FDA reports)
PAIN ( 1138 FDA reports)
NAUSEA ( 655 FDA reports)
BACK PAIN ( 634 FDA reports)
DIZZINESS ( 578 FDA reports)
ABDOMINAL PAIN UPPER ( 575 FDA reports)
ARTHRALGIA ( 538 FDA reports)
DYSMENORRHOEA ( 528 FDA reports)
HYPERSENSITIVITY ( 475 FDA reports)
PRURITUS ( 441 FDA reports)
SOMNOLENCE ( 434 FDA reports)
ABDOMINAL DISCOMFORT ( 420 FDA reports)
FEELING ABNORMAL ( 415 FDA reports)
DYSPNOEA ( 370 FDA reports)
VOMITING ( 363 FDA reports)
URTICARIA ( 355 FDA reports)
PAIN IN EXTREMITY ( 326 FDA reports)
INSOMNIA ( 311 FDA reports)
FATIGUE ( 305 FDA reports)
BLOOD PRESSURE INCREASED ( 293 FDA reports)
EUPHORIC MOOD ( 286 FDA reports)
OEDEMA PERIPHERAL ( 281 FDA reports)
DYSPEPSIA ( 279 FDA reports)
RASH ( 248 FDA reports)
DIARRHOEA ( 246 FDA reports)
MALAISE ( 234 FDA reports)
CONSTIPATION ( 233 FDA reports)
ERYTHEMA ( 229 FDA reports)
MUSCLE SPASMS ( 218 FDA reports)
ASTHENIA ( 213 FDA reports)
SWELLING FACE ( 213 FDA reports)
TOOTHACHE ( 192 FDA reports)
ABDOMINAL PAIN ( 190 FDA reports)
CHEST PAIN ( 187 FDA reports)
ANXIETY ( 163 FDA reports)
HAEMATOCHEZIA ( 161 FDA reports)
MIGRAINE ( 158 FDA reports)
HYPOAESTHESIA ( 156 FDA reports)
LIP SWELLING ( 154 FDA reports)
LOSS OF CONSCIOUSNESS ( 152 FDA reports)
FOREIGN BODY ( 150 FDA reports)
PRURITUS GENERALISED ( 145 FDA reports)
ARTHRITIS ( 143 FDA reports)
MUSCULOSKELETAL PAIN ( 132 FDA reports)
PARAESTHESIA ( 129 FDA reports)
THROAT IRRITATION ( 125 FDA reports)
FEELING HOT ( 122 FDA reports)
UNEVALUABLE EVENT ( 122 FDA reports)
CONTUSION ( 115 FDA reports)
PYREXIA ( 115 FDA reports)
TREMOR ( 111 FDA reports)
PALPITATIONS ( 108 FDA reports)
ABDOMINAL DISTENSION ( 106 FDA reports)
DRUG DEPENDENCE ( 101 FDA reports)
MYALGIA ( 100 FDA reports)
NECK PAIN ( 100 FDA reports)
HYPERHIDROSIS ( 99 FDA reports)
RASH MACULAR ( 98 FDA reports)
RECTAL HAEMORRHAGE ( 98 FDA reports)
NERVOUSNESS ( 96 FDA reports)
EPISTAXIS ( 95 FDA reports)
BURNING SENSATION ( 94 FDA reports)
FAECES DISCOLOURED ( 92 FDA reports)
COUGH ( 91 FDA reports)
EYE SWELLING ( 87 FDA reports)
HEART RATE INCREASED ( 87 FDA reports)
SWOLLEN TONGUE ( 85 FDA reports)
WEIGHT INCREASED ( 85 FDA reports)
DEPRESSION ( 84 FDA reports)
HYPERTENSION ( 82 FDA reports)
FLUSHING ( 81 FDA reports)
JOINT SWELLING ( 81 FDA reports)
BLOOD URINE PRESENT ( 79 FDA reports)
PHARYNGEAL OEDEMA ( 79 FDA reports)
ANAEMIA ( 78 FDA reports)
DRUG HYPERSENSITIVITY ( 77 FDA reports)
DYSGEUSIA ( 76 FDA reports)
FLATULENCE ( 75 FDA reports)
OROPHARYNGEAL PAIN ( 75 FDA reports)
DYSPHAGIA ( 74 FDA reports)
VISION BLURRED ( 74 FDA reports)
WEIGHT DECREASED ( 74 FDA reports)
GAIT DISTURBANCE ( 72 FDA reports)
SYNCOPE ( 72 FDA reports)
GASTRIC ULCER ( 71 FDA reports)
BLISTER ( 70 FDA reports)
BLOOD GLUCOSE INCREASED ( 70 FDA reports)
SWELLING ( 70 FDA reports)
CEREBROVASCULAR ACCIDENT ( 69 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 68 FDA reports)
URINARY TRACT INFECTION ( 67 FDA reports)
CHILLS ( 66 FDA reports)
HAEMORRHAGE ( 66 FDA reports)
ANAPHYLACTIC SHOCK ( 65 FDA reports)
CHEST DISCOMFORT ( 65 FDA reports)
MYOCARDIAL INFARCTION ( 65 FDA reports)
DEEP VEIN THROMBOSIS ( 63 FDA reports)
GASTRIC DISORDER ( 63 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 63 FDA reports)
CHOLELITHIASIS ( 62 FDA reports)
FEELING JITTERY ( 62 FDA reports)
THROAT TIGHTNESS ( 62 FDA reports)
DRY MOUTH ( 61 FDA reports)
MEDICATION ERROR ( 61 FDA reports)
FALL ( 60 FDA reports)
HAEMATEMESIS ( 60 FDA reports)
PULMONARY EMBOLISM ( 59 FDA reports)
BLOOD PRESSURE DECREASED ( 58 FDA reports)
INJURY ( 56 FDA reports)
ADVERSE EVENT ( 55 FDA reports)
MUSCULAR WEAKNESS ( 55 FDA reports)
OVERDOSE ( 54 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 53 FDA reports)
TINNITUS ( 50 FDA reports)
CONVULSION ( 49 FDA reports)
GASTRIC HAEMORRHAGE ( 49 FDA reports)
RENAL FAILURE ( 49 FDA reports)
OCULAR HYPERAEMIA ( 48 FDA reports)
RASH GENERALISED ( 48 FDA reports)
PNEUMONIA ( 47 FDA reports)
CHOLECYSTITIS CHRONIC ( 46 FDA reports)
CONFUSIONAL STATE ( 45 FDA reports)
GASTRITIS ( 45 FDA reports)
RASH ERYTHEMATOUS ( 45 FDA reports)
BALANCE DISORDER ( 44 FDA reports)
ANAPHYLACTIC REACTION ( 43 FDA reports)
DECREASED APPETITE ( 43 FDA reports)
ULCER HAEMORRHAGE ( 43 FDA reports)
CHROMATURIA ( 42 FDA reports)
DEATH ( 42 FDA reports)
DRUG SCREEN POSITIVE ( 42 FDA reports)
GENERALISED ERYTHEMA ( 42 FDA reports)
INFLUENZA LIKE ILLNESS ( 42 FDA reports)
ORAL DISCOMFORT ( 42 FDA reports)
CHOKING ( 40 FDA reports)
DEHYDRATION ( 39 FDA reports)
GLOSSODYNIA ( 39 FDA reports)
HYPOTENSION ( 39 FDA reports)
SKIN DISCOLOURATION ( 39 FDA reports)
HAEMOGLOBIN DECREASED ( 38 FDA reports)
HYPOAESTHESIA ORAL ( 38 FDA reports)
ALOPECIA ( 37 FDA reports)
RASH PAPULAR ( 37 FDA reports)
MOBILITY DECREASED ( 36 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 36 FDA reports)
SPEECH DISORDER ( 36 FDA reports)
WHEEZING ( 36 FDA reports)
RENAL IMPAIRMENT ( 35 FDA reports)
ABASIA ( 34 FDA reports)
EYE PRURITUS ( 34 FDA reports)
FEELING COLD ( 34 FDA reports)
HAEMOPTYSIS ( 34 FDA reports)
POLLAKIURIA ( 34 FDA reports)
RENAL DISORDER ( 34 FDA reports)
RESTLESSNESS ( 34 FDA reports)
THROMBOSIS ( 34 FDA reports)
DRUG EFFECT DECREASED ( 33 FDA reports)
GALLBLADDER DISORDER ( 33 FDA reports)
INCORRECT DOSE ADMINISTERED ( 33 FDA reports)
RETCHING ( 33 FDA reports)
STOMACH DISCOMFORT ( 33 FDA reports)
DISTURBANCE IN ATTENTION ( 32 FDA reports)
DYSURIA ( 32 FDA reports)
FEELING DRUNK ( 32 FDA reports)
GASTROINTESTINAL DISORDER ( 32 FDA reports)
SLEEP DISORDER ( 32 FDA reports)
VAGINAL HAEMORRHAGE ( 32 FDA reports)
CONDITION AGGRAVATED ( 31 FDA reports)
EAR PAIN ( 31 FDA reports)
PAIN IN JAW ( 31 FDA reports)
SCIATICA ( 31 FDA reports)
SINUSITIS ( 31 FDA reports)
INITIAL INSOMNIA ( 30 FDA reports)
ORAL PAIN ( 30 FDA reports)
PANIC ATTACK ( 30 FDA reports)
PARAESTHESIA ORAL ( 30 FDA reports)
ULCER ( 30 FDA reports)
VISUAL IMPAIRMENT ( 30 FDA reports)
OEDEMA ( 29 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 29 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 29 FDA reports)
SKIN BURNING SENSATION ( 29 FDA reports)
DYSARTHRIA ( 28 FDA reports)
EMOTIONAL DISTRESS ( 28 FDA reports)
FLUID RETENTION ( 28 FDA reports)
HALLUCINATION ( 28 FDA reports)
HYPERSOMNIA ( 28 FDA reports)
NIGHT SWEATS ( 28 FDA reports)
SKIN DISORDER ( 28 FDA reports)
STRESS ( 28 FDA reports)
CELLULITIS ( 27 FDA reports)
ABNORMAL DREAMS ( 26 FDA reports)
ASTHMA ( 26 FDA reports)
CARDIAC DISORDER ( 26 FDA reports)
EYE PAIN ( 26 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 26 FDA reports)
INJECTION SITE ERYTHEMA ( 26 FDA reports)
INJECTION SITE PAIN ( 26 FDA reports)
MEMORY IMPAIRMENT ( 26 FDA reports)
NEUROPATHY PERIPHERAL ( 26 FDA reports)
SKIN EXFOLIATION ( 26 FDA reports)
STOMATITIS ( 26 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
AGITATION ( 25 FDA reports)
BONE DISORDER ( 25 FDA reports)
DRUG ADMINISTRATION ERROR ( 25 FDA reports)
MIDDLE INSOMNIA ( 25 FDA reports)
MUSCLE TWITCHING ( 25 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 25 FDA reports)
ATRIAL FIBRILLATION ( 24 FDA reports)
EYELID OEDEMA ( 24 FDA reports)
FIBROMYALGIA ( 24 FDA reports)
HEART RATE IRREGULAR ( 24 FDA reports)
MUSCLE STRAIN ( 24 FDA reports)
PALLOR ( 24 FDA reports)
ANALGESIC THERAPY ( 23 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 23 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 23 FDA reports)
DISCOMFORT ( 23 FDA reports)
OSTEOMYELITIS ( 23 FDA reports)
RENAL INJURY ( 23 FDA reports)
RENAL PAIN ( 23 FDA reports)
APHAGIA ( 22 FDA reports)
FEAR ( 22 FDA reports)
HEPATIC STEATOSIS ( 22 FDA reports)
HOT FLUSH ( 22 FDA reports)
RHEUMATOID ARTHRITIS ( 22 FDA reports)
RHINORRHOEA ( 22 FDA reports)
SENSATION OF FOREIGN BODY ( 22 FDA reports)
SNEEZING ( 22 FDA reports)
AMNESIA ( 21 FDA reports)
BONE PAIN ( 21 FDA reports)
COGNITIVE DISORDER ( 21 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
DYSPHONIA ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
LYMPHADENOPATHY ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
PRODUCT QUALITY ISSUE ( 21 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 21 FDA reports)
VISUAL ACUITY REDUCED ( 21 FDA reports)
EATING DISORDER ( 20 FDA reports)
EYE IRRITATION ( 20 FDA reports)
MELAENA ( 20 FDA reports)
OESOPHAGITIS ( 20 FDA reports)
RASH PRURITIC ( 20 FDA reports)
URINARY INCONTINENCE ( 20 FDA reports)
DIVERTICULUM INTESTINAL ( 19 FDA reports)
DYSSTASIA ( 19 FDA reports)
FOREIGN BODY TRAUMA ( 19 FDA reports)
HAEMORRHOIDS ( 19 FDA reports)
HIATUS HERNIA ( 19 FDA reports)
IMPAIRED HEALING ( 19 FDA reports)
MENTAL IMPAIRMENT ( 19 FDA reports)
PROCEDURAL PAIN ( 19 FDA reports)
ABNORMAL BEHAVIOUR ( 18 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
CHOKING SENSATION ( 18 FDA reports)
CRYING ( 18 FDA reports)
DRY SKIN ( 18 FDA reports)
ERUCTATION ( 18 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 18 FDA reports)
HYPOAESTHESIA FACIAL ( 18 FDA reports)
LETHARGY ( 18 FDA reports)
LIVER DISORDER ( 18 FDA reports)
NASOPHARYNGITIS ( 18 FDA reports)
NIGHTMARE ( 18 FDA reports)
ORAL PRURITUS ( 18 FDA reports)
POOR QUALITY SLEEP ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
ABDOMINAL PAIN LOWER ( 17 FDA reports)
CATARACT ( 17 FDA reports)
CROHN'S DISEASE ( 17 FDA reports)
DENTAL CARIES ( 17 FDA reports)
FACIAL PAIN ( 17 FDA reports)
GINGIVAL INFECTION ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 17 FDA reports)
INJECTION SITE HAEMATOMA ( 17 FDA reports)
LACRIMATION INCREASED ( 17 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 17 FDA reports)
OEDEMA MOUTH ( 17 FDA reports)
OESOPHAGEAL PAIN ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
RENAL FAILURE CHRONIC ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
ANGER ( 16 FDA reports)
ANOREXIA ( 16 FDA reports)
BONE DEBRIDEMENT ( 16 FDA reports)
CHAPPED LIPS ( 16 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 16 FDA reports)
HEART RATE DECREASED ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
PRIMARY SEQUESTRUM ( 16 FDA reports)
RESTLESS LEGS SYNDROME ( 16 FDA reports)
SINUS HEADACHE ( 16 FDA reports)
TACHYCARDIA ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
EPIGASTRIC DISCOMFORT ( 15 FDA reports)
FISTULA ( 15 FDA reports)
HAEMORRHAGIC DIATHESIS ( 15 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
HUNGER ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
MOOD ALTERED ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 15 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
ANGINA PECTORIS ( 14 FDA reports)
BLOOD POTASSIUM INCREASED ( 14 FDA reports)
BRONCHITIS ( 14 FDA reports)
CHEILITIS ( 14 FDA reports)
DISORIENTATION ( 14 FDA reports)
DRUG DOSE OMISSION ( 14 FDA reports)
DYSPNOEA EXERTIONAL ( 14 FDA reports)
FACE OEDEMA ( 14 FDA reports)
GASTROINTESTINAL ULCER ( 14 FDA reports)
INTESTINAL HAEMORRHAGE ( 14 FDA reports)
METRORRHAGIA ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NON-CARDIAC CHEST PAIN ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
SCAR ( 14 FDA reports)
STAPHYLOCOCCAL INFECTION ( 14 FDA reports)
ACCIDENTAL EXPOSURE ( 13 FDA reports)
ANHEDONIA ( 13 FDA reports)
APHASIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
ERECTILE DYSFUNCTION ( 13 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 13 FDA reports)
FUNGAL INFECTION ( 13 FDA reports)
HEAD DISCOMFORT ( 13 FDA reports)
LIMB DISCOMFORT ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
NEURALGIA ( 13 FDA reports)
PALMAR ERYTHEMA ( 13 FDA reports)
PROCTALGIA ( 13 FDA reports)
SENSATION OF HEAVINESS ( 13 FDA reports)
SKIN WARM ( 13 FDA reports)
SOFT TISSUE INFECTION ( 13 FDA reports)
THINKING ABNORMAL ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
WOUND DEHISCENCE ( 13 FDA reports)
ABSCESS JAW ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
BASAL CELL CARCINOMA ( 12 FDA reports)
BLOOD DISORDER ( 12 FDA reports)
BLOOD TEST ABNORMAL ( 12 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CHOLECYSTITIS ( 12 FDA reports)
COLITIS ULCERATIVE ( 12 FDA reports)
COLONOSCOPY ABNORMAL ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
INCISIONAL DRAINAGE ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
MOVEMENT DISORDER ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
PULMONARY FIBROSIS ( 12 FDA reports)
PURULENCE ( 12 FDA reports)
SHOCK ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
TOOTH DISCOLOURATION ( 12 FDA reports)
TOOTH FRACTURE ( 12 FDA reports)
TOOTH LOSS ( 12 FDA reports)
ABDOMINAL TENDERNESS ( 11 FDA reports)
BLINDNESS TRANSIENT ( 11 FDA reports)
BLOOD PRESSURE ABNORMAL ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
CARDIOVASCULAR DISORDER ( 11 FDA reports)
COLD SWEAT ( 11 FDA reports)
DEPRESSED MOOD ( 11 FDA reports)
DRUG ABUSER ( 11 FDA reports)
DRY EYE ( 11 FDA reports)
ECZEMA ( 11 FDA reports)
GROIN PAIN ( 11 FDA reports)
HAEMORRHAGE URINARY TRACT ( 11 FDA reports)
HEMIPLEGIA ( 11 FDA reports)
HYPERCHLORHYDRIA ( 11 FDA reports)
HYPOXIA ( 11 FDA reports)
INFECTION ( 11 FDA reports)
INFLUENZA ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
MENTAL DISORDER ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
TOOTH DISORDER ( 11 FDA reports)
TREATMENT NONCOMPLIANCE ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
VISUAL DISTURBANCE ( 11 FDA reports)
ABSCESS ( 10 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
ARTERIOSCLEROSIS ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
COAGULOPATHY ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DRUG INTOLERANCE ( 10 FDA reports)
DRY THROAT ( 10 FDA reports)
FAECAL INCONTINENCE ( 10 FDA reports)
GASTROINTESTINAL PAIN ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
IRRITABLE BOWEL SYNDROME ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
MENSTRUATION IRREGULAR ( 10 FDA reports)
MULTIPLE SCLEROSIS ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
MUSCLE TIGHTNESS ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PELVIC PAIN ( 10 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 10 FDA reports)
PRODUCTIVE COUGH ( 10 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SKIN WRINKLING ( 10 FDA reports)
SLUGGISHNESS ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
AFFECT LABILITY ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
ARTHROPATHY ( 9 FDA reports)
AZOTAEMIA ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
COELIAC DISEASE ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEFORMITY ( 9 FDA reports)
DERMATITIS ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
ENERGY INCREASED ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
METASTASES TO BONE ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
NASAL OEDEMA ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
ORAL HERPES ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
SCRATCH ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SELF-INJURIOUS IDEATION ( 9 FDA reports)
SKIN TIGHTNESS ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
TENDON PAIN ( 9 FDA reports)
THIRST ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
AMENORRHOEA ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
AURICULAR SWELLING ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BURSITIS ( 8 FDA reports)
CHOLECYSTECTOMY ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
COMA ( 8 FDA reports)
CYSTITIS ( 8 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 8 FDA reports)
DIPLOPIA ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
FOAMING AT MOUTH ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GENITAL RASH ( 8 FDA reports)
GOUT ( 8 FDA reports)
HOMICIDAL IDEATION ( 8 FDA reports)
HYPOACUSIS ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INCREASED TENDENCY TO BRUISE ( 8 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
NASAL DRYNESS ( 8 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
OSTEOSCLEROSIS ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PHOTOPSIA ( 8 FDA reports)
PLEURITIC PAIN ( 8 FDA reports)
PRURITUS GENITAL ( 8 FDA reports)
ROAD TRAFFIC ACCIDENT ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN HYPERTROPHY ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
URINE ODOUR ABNORMAL ( 8 FDA reports)
URTICARIA GENERALISED ( 8 FDA reports)
VASCULAR RUPTURE ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ASTHENOPIA ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DEPENDENCE ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
FAECES HARD ( 7 FDA reports)
GASTRITIS EROSIVE ( 7 FDA reports)
GOITRE ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HYPERVIGILANCE ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
LIBIDO DECREASED ( 7 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
MICTURITION FREQUENCY DECREASED ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OESOPHAGEAL DISCOMFORT ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OVARIAN CYST ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
RETINAL HAEMORRHAGE ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SYNOVIAL CYST ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ACUTE SINUSITIS ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BONE SWELLING ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
BREAST MASS ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CHOLESTEROSIS ( 6 FDA reports)
CLUMSINESS ( 6 FDA reports)
COLITIS ( 6 FDA reports)
CYST ( 6 FDA reports)
DENTURE WEARER ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DIZZINESS POSTURAL ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
EAR PRURITUS ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
GALLBLADDER INJURY ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
LOCAL SWELLING ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PAINFUL RESPIRATION ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TENSION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TONGUE PRURITUS ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
UTERINE PAIN ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ALCOHOL INTERACTION ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BLADDER CANCER STAGE III ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BONE OPERATION ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
BREATH ODOUR ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DRUG EFFECT DELAYED ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FEELING OF RELAXATION ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
JAW OPERATION ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
ORAL SURGERY ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
POOR DENTAL CONDITION ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TONGUE DRY ( 5 FDA reports)
TONGUE INJURY ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
UTERINE LEIOMYOMA ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ANALGESIA ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BURNING SENSATION MUCOSAL ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DROOLING ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EPICONDYLITIS ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
GASTRIC INFECTION ( 4 FDA reports)
GASTRIC PH DECREASED ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HERNIA PAIN ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HOMANS' SIGN ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUTISM ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PENILE BLISTER ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PURPURA ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL HAEMORRHAGE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
SCAB ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE EROSION ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 3 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GENITAL ERYTHEMA ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEMICEPHALALGIA ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OSTEORADIONECROSIS ( 3 FDA reports)
PANCREATOLITHIASIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PRURITUS ANI ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL INFARCTION ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATROPHIC GLOSSITIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BENIGN VAGINAL NEOPLASM ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE MATERIAL ISSUE ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GENITAL DISORDER MALE ( 2 FDA reports)
GENITAL INJURY ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BILIARY TRACT ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PSEUDOPOLYPOSIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 2 FDA reports)
REFLUX LARYNGITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL CYST ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
STARING ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TIC ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLAR INFLAMMATION ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL ALLERGY ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER POLYPECTOMY ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE FREE ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARNITINE PALMITOYLTRANSFERASE DEFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PRURITUS MALE ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTED VARICOSE VEIN ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT USED FOR UNKNOWN INDICATION ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEMINAL VESICULITIS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOMATIC HALLUCINATION ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERMOHYPOAESTHESIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE PIGMENTATION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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